Clinical Operations Jobs in Pharma & Biotech

The OPIC Project Coordinator V provides essential administrative support, ensuring smooth operations and efficiency within the organization. This role involves managing and leveraging technology platforms to streamline processes and enhance productivity. Additionally, the Project Coordinator V serves as the office liaison for OPIC Minneapolis sites, facilitating communication and coordination among various stakeholders. Provide comprehensive project support to OPIC, including Compiling and preparing reports and materials for recurring meetings. Managing projects, documentation, and communication for compliance initiatives (e.g., compliance training launches, ethics and integrity culture programs, Sunshine reporting). Deliver advanced administrative support to the SVP, Chief Privacy, Compliance & Integrity Officer,...

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...

#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...

#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...

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...

The Clinical Trial Manager is responsible for the overall management, planning, implementation, and execution of clinical trial(s) in a fast-paced environment with moderate oversight from the Senior Clinical Trial Managers and/or Associate Director, Clinical Operations. Key Responsibilities Include Leads and/or assists the trial team to execute and deliver the clinical trial in accordance with the clinical development plan/strategy, budget and timeline. Author clinical trial documents and trial-related plans. Contributes to and/or approves with oversight, the clinical review of CRFs, CRF completion guidelines, and the data review plan. Leads/assists in the identification and selection of investigator sites. Responsible for planning, conducting,...

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...

Manages administrative functions related to the full-lifecycle recruitment process. Serves as the subject matter expert as it pertains to interview scheduling, recruiting systems, and expense report submission. Primary Responsibilities Executes and oversees interview scheduling logistics in a timely and professional manner. Proactively follows up with candidates and hiring teams as changes arise to ensure a seamless recruiting process. Ensures a positive candidate experience and adherence by interviewers to Acadia Talent Acquisition processes and policies. Administer Acadia’s travel program for onsite candidate interviews. Manages background checks and references, and transitions pending new hires to People and Performance Operations. Supports Greenhouse systems...

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 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...

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...

This is a dynamic Project Coordinator role supporting the VP & Chief Medical Officer and VP of Medical Affairs for the global Cardiac Rhythm Management (CRM) Clinical and Medical Affairs organization. The CRM Operating Unit (OU) is the longest standing business within Medtronic that aims to help patients with heart rhythm disturbances. The Clinical & Medical Affairs organization is a global team of over 200 individuals focused on generating evidence, educating and building strong scientific relationships with health care professionals. This role will report directly to the CRM Chief Medical Officer/VP of Medical Affairs to drive and support the daily...

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 ·...

The Senior CRA will enable AbbVie’ s emergence as a world class R&D organization, the position plays a key role in ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies. Responsibilities For assigned sites/study(s), ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out. Ensure site related study execution including but not limited to monitoring visits, site evaluations, site selection, and activation, and monitoring close out and visit reports. Anticipate and identify site issues that could affect timelines and develop alternative solutions. Ensure clinical trial management systems containing all site-specific information...

The CRA II advances AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. They partner with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. Lastly, the CRA II focuses on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing...

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...

As an Endoscopy Clinical Research Specialist (CRS), you will manage the daily operations of key market adoption studies and novel data collection activities. This position should be able to function with minimal supervision, handling various clinical study assignments and collaborating with cross-functional colleagues and external physicians in resolution of strategic and operational issues. The Endoscopy operating unit improves patient outcomes by empowering every gastroenterologist across the globe with artificial intelligence and disruptive therapeutic technologies. We develop diagnostic and therapeutic solutions that enable early detection and treatment of gastrointestinal diseases and cancers. As an Endoscopy Clinical Research Specialist (CRS), you will...

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...

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...

This position is responsible for providing high volume call center support and best in class customer service to patients and health care providers. This role will be responsible for educating patients on the enrollment process, handling status inquiries along with scheduling deliveries. This position uses the core CRM system to manage workload, perform activities and route work to other members of the team. Responsibilities Provide subject matter expertise of program requirements and application status while maintaining a high level of customer service, sense of urgency, reliability, data entry skills, active listening, proper phone etiquette, great verbal and writing skills, and...

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...

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,...

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)...

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,...

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...

Are you looking for a Warehouse Management opportunity where you will ensure all products are distributed correctly and inventory is maintained? If so, this is the role for you. As a Warehouse Inventory Coordinator , you will be responsible for assisting the Warehouse Supervisor in coordinating the activities Inventory Control and the effective flow of materials in the warehouse unit. This role will support a team of Warehouse Associates who carry out the daily activities of the areas (including, but not limited to, warehouse and non-warehouse inventory control, incoming GMP and non-GMP material movements, shipping and receiving) through on the...

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,...

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. Through the application of scientific and clinical training and expertise, the...

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...

In this exciting role as a Clinical Research Manager (CRM) , you will have primary focus responsibility to oversee all clinical activities related to one or more clinical studies and performing/directing/managing the daily in-house activities associated with the studies. This is a people leadership role. The CRM will report to the US Sr. Clinical Research Director and independently handle various clinical study assignments, have management responsibility, and oversees and directs the work of a team of Clinical Research Specialists at all levels, from entry level to tenured. Responsibilities may include the following and other duties may be assigned. Provides leadership...

Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. Our company's Neuroscience Medicines span all phases of clinical development (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical...

Generate Biomedicines is seeking an experienced and collaborative Senior Clinical Trial Manager (Sr. CTM) to lead the execution of Phase 3 clinical trials within our Clinical Development team. This role will report to the Sr. Director of Late Stage Clinical Operations and be responsible for managing global, late-stage studies intended to support regulatory submissions and eventual product approval. The Sr. CTM will work cross-functionally across Clinical Development, Regulatory Affairs, Clinical Supply, and Data Management, while serving as a key point of contact for CROs, vendors, and clinical sites. This is a critical role for ensuring operational excellence, compliance, and delivery...

POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *Please note this will be a clinic...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, 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 plans and Investigational New...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your...

Johnson & Johnson MedTech, Electrophysiology, is recruiting a Clinical Research Manager. This role is based in Irvine, CA on a hybrid work schedule onsite 2-3 days a week. 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....

Make a difference in patients' lives by applying your diagnostic and clinical test market expertise as a Precision Medicine Liaison! Key responsibilities include ensuring the timely, high quality in-market companion diagnostics / testing solutions are available to support optimal treatment. Engage collaborators before and after launch to provide approved information to proactively address barriers to testing at pre-specified region reference labs, pathology medical groups and a subset of academic/health system with well-developed diagnostic and molecular capabilities within assigned geography. Act as the regional expert to support oncology customers at the request of the cross functional team by providing more in-depth...

Your skills could be critical in helping our teams accelerate progress. Position Overview 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 rheumatologic diseases, incorporate new methodologies, and pro-actively progress study execution. The role will focus on developing innovative therapies for autoimmune and inflammatory diseases, with a particular emphasis on rheumatology. We are an innovative global...

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 The Associate Director/Director, Clinical Trial Foundations (CTF), will serve as...

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. The Senior Director, Clinical Development will lead clinical development program(s)...