Clinical Operations Jobs in Pharma & Biotech

We have an exciting opportunity for an Administrative Coordinator at HHMI working in the Science Operations Office located at Stanford University in Stanford, California. The role involves assisting the Science Operations Services (SOS) in the delivery of financial, procurement and lab management services to assigned HHMI research laboratories at Stanford. This is an opportunity to work at a world class research organization, supporting science that is fundamentally changing how we look at and interact with the world around us. We are ideally targeting a self-motivated, curious, and responsible candidate. This role serves as an integral part of the operational support...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose Through the application of scientific and medical training, clinical expertise,...

Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as accessioning, processing, automation usage, sample racking,...

This Clinical Research Associate works remote but must be based in Illinois. We are seeking an experienced professional individual contributor to join our team and oversee the direction, planning, execution, and data collection activities of clinical trials/research. This role operates under limited supervision and requires the application of subject matter knowledge in Medical Affairs. This role will support our Abbott Diagnostics division. What You’ll Work On Contribute to the implementation of clinical protocols and facilitate the completion of final reports. Recruit clinical investigators and negotiate study design and costs. Direct human clinical trials (phases III & IV) for company products...

The CoreValve Principal Therapy Development Specialist (TDS) provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-Based Therapies (CBT) and CVG field organizations to drive procedural and practice success. Technical and Clinical Expertise Provide clinical expertise for TAVR implanting centers, including “scrubbing in” for TAVI implant procedures to assist with loading valves onto delivery catheter, and providing technical support in accordance with the instructions for use/trial protocol, and best -practices to facilitate procedural...

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day “What would I do if this patient were my mom?” That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a...

AbbVie is committed to being an industry leader in accelerating the transformation of molecules to medicines to maximize the value for patients and AbbVie. To do so, we must have a clear strategy to attract underserved, diverse populations of investigator sites and patients to improve representation in our clinical trials. The Clinical Trial Diversity & Inclusion Sr. Manager sits within the Clinical Development Operations (CDO) organization and is responsible for driving the implementation of AbbVie’s enterprise-wide plan to improve clinical trial diversity. With this role, you will be an important member of the team that will be driving change in...

The Strategic Medical Writing Operations Team is dedicated to delivering high-quality, scientifically accurate, and strategically aligned clinical and regulatory documentation that supports AbbVie's mission to transform the standard of care. Our team serves as a critical link between research, development, and regulatory submissions, ensuring clarity and compliance in all clinical and regulatory documents. We strive to innovate and enhance the processes of medical writing through cross-functional collaboration, agile methodologies, and the integration of cutting-edge technology, driving forward AbbVie's commitment to improving patient outcomes worldwide. Responsibilities Responsible for the formatting, report publishing and coordination of the Clinical Study Reports (CSR) Appendices...

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day “What would I do if this patient were my mom?” That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a...

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self, and live a full life. You’ll also have access to Career development with an international company where you can grow the career you dream of Free medical coverage for employees* via the Health Investment Plan (HIP) PPO An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work...

Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and...

Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and helping people live longer,...

Accountable for all country clinical/medical aspects associated with Development and prioritized research programs/trials by providing clinical strategic and tactical leadership as the Country Clinical Development representative. Major Accountabilities From Strategy to Functional Excellence Provides Clinical Development and indication expertise specific to Country, and together with the clinical trial operations team, drives the execution of clinical trials with high quality and within planned timelines · Actively contributes to scientific/clinical/medical aspects of the start-up phase to ensure fast clinical trial site start-up. · Develops clinical/medical trial plans taking the broader ecosystem into account for assigned programs/trials to ensure successful trial implementation,...

Johnson and Johnson is currently seeking a Clinical Research Scientist to JJMT Electrophysiology. This role is based in Irvine, CA and reports to the office on assigned days 2-3 times per week. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and...

Johnson and Johnson is currently seeking a Staff Clinical Research Scientist to support the scientific publication medical writing needs of the Electrophysiology business. This role is based in Irvine, CA and reports to the office on assigned days 2-3 times per week. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of...

Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as accessioning, processing, automation usage, sample racking,...

Johnson & Johnson MedTech Electrophysiology is recruiting for a Clinical Research, Manager, to support the Electrophysiology (EP) business unit based in Irvine, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at Fueled...

Johnson & Johnson MedTech Electrophysiology is recruiting for a Clinical Research, Manager, to support the Electrophysiology (EP) business unit based in Irvine, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at Fueled...

Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and helping people live longer,...

The Senior Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study...

The Senior Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study...

Internal Project Coordinator CEO of Communications & Operations A Day in the Life In this highly visible role, you will provide comprehensive administrative and project coordination support to the Vice President of CEO Communications & Operations and their team. You will serve as a trusted partner, ensuring seamless operations, effective communication, and efficient execution of priorities. This includes managing complex scheduling, preparing executive materials, organizing meetings and events, and supporting departmental projects. The role requires a proactive, detail-oriented professional who thrives in a fast-paced environment and can balance multiple priorities with discretion and professionalism. At Medtronic, we bring bold...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Clinical Research Physician – Medical Affairs - Oncology Purpose At Lilly,...

JOB SUMMARY The Clinical Research Nursing Provider is a member of the Pfizer Clinical Research Unit which is a global organization with Clinical Research Units in New Haven, CT and Brussels, Belgium. The Clinical Research Units operate for the purpose of conducting early clinical trials with healthy volunteers. This individual assures and is responsible for data and sample collection and safety of the trial subjects. This individual focuses on the clinical nursing requirements of PCRU study protocols that yield reliable, high quality research outcomes, and valid scientific data and findings. This individual is also responsible for performing self-daily check on...

We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The Congenital Therapies Therapy Development Specialist provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic Congenital Therapies System and therapy technologies. The Congenital Therapies Therapy Development Specialist works closely with implanting teams and the Medtronic Heart Valve Therapies and CVG field...

Peripheral Vascular Health therapies treat patients with Peripheral and Carotid Artery Disease, End-Stage Renal Disease, Superficial and Deep Venous Diseases, and a variety of conditions treated with Peripheral Embolization. The operating unit leads the way in the Superficial Venous, Deep Venous Stenting, and Drug-Coated Balloon markets, caring for nearly 1 million patients globally with lifesaving and life-enhancing therapies. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to...

Key Responsibilities In the role as Associate Director, Companion Diagnostics Program Management within Precision Medicine and Translational Science, the ideal candidate Responsibilities may vary based on project and stages of development (early, late, and lifecycle) Manage the implementation of Biomarker Strategies and Companion Diagnostic projects to support global Development Teams Responsible for managing the Precision Medicine project team and deliverables, working effectively with cross-functional representatives including scientific, clinical, regulatory, legal, finance Responsible for developing and coordinating resource planning across functions to assure that adequate resources are being applied to the project Develop and maintain timelines for Precision Medicine activities, assure...

We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The CoreValve Therapy Development Specialist provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-based Therapies (CBT) and CVG field organizations...

Johnson & Johnson MedTech - Electrophysiology division is currently seeking a Clinical Research Leader (PM) position. This position is located in Irvine, California and has a hybrid work schedule of 3 days a week on-site. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of...

Scientific Director – Pathologist, Translational Pathology, Precision Medicine What you will do The use of Biomarkers and Diagnostics is central to understanding how our therapeutics work and identifying patients that benefit most from these therapies. Accordingly, the Precision Medicine (PMED) function plays a critical role in advancing our drug development programs and is accountable for the development of biomarker and diagnostics strategy across our pipeline. The PMED Translational Pathology group is responsible for implementing the biomarker and diagnostics strategies. We are seeking a highly motivated individual to provide pathology expertise and help drive implementation of tissue-based assays including digital...

Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and helping people live longer,...

Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and helping people live longer,...

The Senior Country Coordinator (CC) provides administrative support to the conduct of clinical trials conducted by Regional Clinical Operations (RCO) from study start-up to study closure; and may include administrational support to the RCO Regional Heads, Head of RDLs, Head of Clinical Operations (HCOs) or Country Heads. Key Responsibilities Study support In line with country requirements, arrange drug and non-drug (Lab kits, ECG, e-COA) importation to support study sites, and where required contact with CSC Logistics for drug shipment. Coordinate, and where applicable, prepare study related documents for printing, sealing, scanning, binding and delivery to site. This includes printing and/or...

#LI-HYBRID This position will be located at the Cambridge, MA or Basel, Switzerland. This position may require up to 5% travel as defined by the business. We are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Trial Leaders (Clinical Scientists) who plan and execute early phase trials worldwide. From First-in-Human to ph2a studies and beyond. We design and operationalize trials, ensuring they run smoothly, on time and – most importantly – with patients’ interests to the fore. Curious, unbossed and inspired; we are committed to flexibility in the workplace. As a member of our team, you will...

#LI-Hybrid Internal Principal Scientist II As a BMD Study Expert in LEO you will be driving patient-centric operational innovation and partnership with external service providers/CROs and internal subject matter experts. Laboratory Excellence and Operation (LEO) is the key global resource for Line functions (LF) and Biomedical Research (BR) Clinical Trial Teams for biomarkers including biomarker outsourcing, scientific bi-omarker monitoring, vendor management, biomarker logistics, clinical site communication and sample coordination. LEO is working in close collaboration with clinical teams, LF technology experts, Biomarker Leads (BMLs) as well as specialized external service providers (ESP), central labs and clinical sites. Key...

Purpose Design, generate and distribute daily, weekly, monthly, and quarterly reports for the team. Maintains departmental files, including headcount reporting and org charts for the team. Updates agenda and presentations for select leadership meetings, such as quarterly business review meetings and bi-monthly all-staff communication meetings. Process purchase orders in SRM, as well as track and review monthly invoices for customer service vendors. Works with Finance and Procurement functions to resolve issues and discrepancies in a timely manner. Track overall expenses for the team, including purchase order spend, travel expenses, and other department expenses. Review and triage customer inquiries in the...

Purpose Responsible for day to day inbound, outbound and third party domestic shipment requests. Accountable for the settings within SAP which control the selection of the carrier for shipments from the AbbVie DCs located in Lake County, IL. The Coordinator will work with the carriers to ensure established turn by turn directions are established for outbound truckload shipments are out of the AbbVie Lake County DC. This individual will use systems to plan and communicate bookings each week, and will keep the stakeholders informed of last minute changes. As the main interface on day to day bookings, this individual will...

In this role, you will serve as an operational liaison by fostering collaborative partnerships between operational and scientific staff. You will need to consistently provide timely, professional, customer-focused service with responsibilities to include various aspects of procurement, budget management, travel, seminar/meeting organization, asset management, and policy communication. You will seamlessly handle and take ownership of a wide variety of situations and tasks, communicate in an easily understood manner, and ensure the efficient management of labs to maximize their time spent conducting research. This position supports science but is similar in nature to a position such as an Office Manager (heavy...

Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and...

Johnson & Johnson MedTech - Electrophysiology division is currently seeking a Clinical Research Manager . This position is located in Irvine, CA with a hybrid work schedule of 2 -3 days a week on-site. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow...

RayzeBio , a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. Summary Located at our Indianapolis, IN facility, The Materials Coordinator will be responsible for supporting the procurement processes related to manufacturing and distribution of clinical trial and commercial products for RayzeBio programs. Responsibilities also include supporting implementation of...

The Material Coordinator 3 (MC3) plays a critical, hands-on role within Illumina’s San Diego Distribution team, responsible for executing a broad range of material handling, inventory, and logistics tasks to support the global movement of temperature-sensitive biotech products. This role requires strong operational knowledge and a proactive mindset, with an emphasis on cross-training and flexibility across multiple departments including Manufacturing, Quality, Planning, and Customer Support. The ideal candidate will be able to move seamlessly between functions, adapt quickly to shifting priorities, and support continuous improvement efforts. Key Responsibilities Perform intermediate to advanced picking, packing, and shipping for domestic and international...

Position Overview The Material Coordinator 2 is responsible for picking, packing, and transacting inventory to support San Diego’s shipments. Order Fulfillment is responsible for various types of requests. This role will also be working with other departments within Distribution. Responsibilities Support picking, packing and shipping of material for order fulfillment by using scanners or by manual methods. Perform shipping functions under general supervision. Responsible for picking and packing all shipments from Illumina. Process orders using various ERP's UPS WorldShip, SAP, JIRA, and FedEx Ship Manager software. Establishes and maintains cooperative relationships within their team and any other departments contacted during...

Johnson & Johnson MedTech - Electrophysiology division is currently seeking a Sr. Clinical Research Specialist . The preferred location is Irvine, CA on a hybrid work schedule of 2 -3 days a week onsite. We are open to remote applicants. W hile specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured,...

Public Affairs Coordinator - Latam - VIE Contract Location Mexico, Mexico City Target start date 01/01/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make...

This role is a new 3rd shift team. This team will TRAIN on 2nd shift ( 345pm - 215am M-Th - 10h). Once trained, likely 1Q26, the team will move to 3rd shift (11pm - 730am M-F 8 hr day). Accountabilities · Coordinate packaging activities for all products as assigned · Work closely with the Process Facilitator to ensure department priorities are met · Understand and follow GMP procedures required to package product to specification · Assign packaging operators to predetermined visual staffing plan · Understand the daily packaging schedule to maintain line operation and adjust schedule if required ·...

A Natera Test Coordinator Phlebotomist serves patients by scheduling and identifying the best method for retrieving blood; preparing specimens for laboratory testing; and reconciling paperwork requirements as needed. *This is an onsite position in Houston, TX* PRIMARY RESPONSIBILITIES PHLEBOTOMY SERVICES Perform venipunctures to obtain blood specimens with precision and care. Verify patient identity and test requisitions, ensuring accuracy by cross-referencing EMR records and resolving discrepancies. Maintain specimen integrity by following aseptic techniques, department protocols, and isolation procedures. Accurately track collected specimens by documenting initials, date, and collection time, while maintaining daily collection logs. PATIENT CARE COORDINATION Oversee...

Senior Principal Scientist, Precision Medicine, Immunology Precision Medicine is an integral part of our Immunology Therapeutic Area. To support our growing Immunology pipeline across Gastroenterology, Rheumatology and Dermatology we are seeking an experienced experimental medicine leader in our newly created Precision Medicine and Diagnostics function. Reporting to the Associate Vice President ,Precision Medicine and Diagnostics, in this role, you will serve as the translational lead on late-stage immunology programs, driving the Precision Medicine objectives in alignment with clinical development plans. Collaborating with Discovery, Translational Medicine and Product Development Teams, you will be the authority in defining and interpreting the translational...

Senior Administrative Coordinator, US Corporate Affairs Location Washington, DC Introduction to role Are you ready to make a significant impact in a dynamic environment? We are seeking a proactive and highly organized Senior Administrative Coordinator to join our US Corporate Affairs team in Washington, DC. This pivotal role involves providing executive-level support to the Vice President of US Corporate Affairs and the team. If you thrive in fast-paced settings and can demonstrate initiative, discretion, and attention to detail, while adapting to evolving business needs, this opportunity is for you! Accountabilities Provide comprehensive administrative support to the Vice President of US...

Johnson & Johnson MedTech - Electrophysiology division is currently seeking to fill two Clinical Research Leader (PM) positions. This position is located in Irvine, California and has a hybrid work schedule of 3 days a week on-site. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the...

Our J&J MedTech Electrophysiology clinical team is currently recruiting for two Sr. Clinical Research Specialists . These roles are based in Irvine, California with a hybrid work schedule of 2 - 3 days a week on-site. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs...

Johnson & Johnson MedTech - Electrophysiology division is currently seeking to fill two Clinical Research Leader positions. This position is located in Irvine, California and has a hybrid work schedule of 3 days a week on-site. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs...

Patient Support Program Coordinator COPAC Ubicación Ciudad de México (Mitikah) 60% presencial Tipo de contrato Indeterminado Acerca de la posición En Sanofi General Medicines , nos dedicamos a mejorar la salud diaria de millones de pacientes en todo el mundo. A pesar de los enormes avances en salud pública, incluso hoy en día, muchos pacientes aún no reciben la atención que necesitan. No solo estamos ayudando a tratar a más pacientes en la actualidad, sino que también estamos haciendo posible la ciencia que proporcionará mejores medicamentos mañana. Estamos transformando nuestro negocio y la forma en que nos relacionamos con nuestros...

About Cardiovascular Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at We are searching for the best talent for...

Functional Area Description The Senior Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a...

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day “What would I do if this patient were my mom?” That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a...

Local Trial Manager What you will do and what we expect of you In this vital role you will Duties Process clinical data, including receipt, entry, verification, or filing of information; Monitor work productivity or quality to ensure compliance with standard operating procedures; Contribute to the compilation, organization, and production of protocols, clinical study reports, regulatory submissions, or other controlled documentation; Read technical literature and participate in continuing education or professional associations to maintain awareness of current database technology and best practices; Provide support and information to functional areas such as marketing, clinical monitoring, and medical affairs; Partner with...

Local Trial Manager What you will do and what we expect of you In this vital role you will Duties Communicate country status including timelines and deliverables to key partners including updates to relevant systems for transparency; Accountable for site-level goal setting and study specific deliverables for clinical sites within their countries; Manage, oversee and supervise applicable vendor activities such as laboratories and equipment provisioning; Contribute and develop program and study-specific materials such as monitoring plan, study specific training documents; Support and contribute to Clinical Study Teams or Trial Management Teams; Partner with global and local country teams to...

The Analyst role is an entry-level position within Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) organization — an internal consulting team dedicated to accelerating clinical development through data-driven analytics and trial planning. As an Analyst, you will be embedded in a project-based delivery team supporting a specific clinical trial. You’ll work under the guidance of more senior team members to help execute feasibility analyses, forecasting models, dashboards, and other core analytics deliverables. You are not expected to be a clinical or therapeutic area expert at the start, but you will be expected to learn quickly, apply structured problem-solving,...

Our J&J MedTech Electrophysiology clinical team is currently recruiting for a Sr.Clinical Research Specialist . This role is based in Irvine, California however we are open to remote candidates within the United States. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and...

The Future Talent Program features internships that lasts up to 12 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals. The Global Clinical Trial Operations (GCTO) team is seeking applicants for the Monitoring Excellence Organization intern position. The intern will engage with the Monitoring Excellence organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of clinical trials across GCTO. Activities may include (but are not limited to)...

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day “What would I do if this patient were my mom?” That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a...

The intern will assist the Pharmacy Services team of Clinical Research Pharmacists (CRPs) in daily operations and any special projects as assigned. The Clinical Research Pharmacist’s primary objective is to provide pharmacy expertise in the development, management, and handling of investigational products at a program and protocol level (e.g. pharmacy manuals for utilization by health care personnel) at clinical sites. Key Responsibilities Working with the assigned Clinical Research Pharmacist (CRP) the intern will have opportunity to perform some of the key Pharmacy Services responsibilities as outlined below; Support pharmacy services strategies and processes for CSC (Clinical Supply Chain) supported clinical...

The Senior Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed cardiovascular and respiratory medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may be responsible for Evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and investigational new drug applications Developing clinical development strategies for investigational or marketed cardiovascular and respiratory drugs Planning clinical trials (design, operational plans, settings) based on...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Organization Overview At Lilly, we serve an extraordinary purpose. We make...

Ready to push the limits of what’s possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world. The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is responsible for the creation of the clinical development plan in alignment with the project strategy, its endorsement by governance and its execution in close collaboration with clinical operations. The CRD is expected to advance scientific and clinical knowledge for immunology in Dermatology, incorporate new methodologies and pro-actively...

The Future Talent Program features internships with a duration of up to 12 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals. The Global Clinical Trial Operations (GCTO) team is seeking applicants for the Epidemiology Operations intern position. The intern will engage with the Epidemiology Operations organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of epidemiology trials across GCTO. Activities may include (but are not limited...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research & Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our clinical team is recruiting for summer interns within the trial manager area of our company. The Trial Data Manager Creates and ensures the successful execution of the clinical data management strategy for assigned trials within a specific drug/vaccine program. Develops and manages project plans which span from protocol development through database...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals. The Diversity and Inclusion in Clinical Trials (DICT) Intern will play a pivotal role in supporting the organization's efforts to enhance representation in clinical trials. The intern will contribute to various initiatives aimed to improve representation inclusive of age, race, ethnicity, sex, gender, socioeconomic background and geography in clinical research. The Internship Program will last up to 12...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research Labs can provide you with great development and a chance to see if we are the right company for your long-term goals. Our company's Global Clinical Trial Operations (GCTO) regional team is currently recruiting for summer interns. GCTO is a global organization operating in over 52 countries and is responsible in the delivery of our company's diverse development portfolio comprising over 300 clinical trials in compliance with global and local regulations. The Regional organization is comprised...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. At Lilly, we unite caring with discovery to make life better...

Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and helping people live longer,...

The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. Location Alameda, CA Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Conduct single or multi-center medical device clinical studies. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items. Participate in study...