Clinical Operations Jobs in Pharma & Biotech

Shipping & Receiving Coordinator - 2nd Shift Round Lake, IL About the role The Shipping & Receiving position is responsible for the efficient storage and movement of materials and finished goods. This role ensures that shipping, receiving, warehousing, and inventory control processes are executed effectively to support Takeda's operational needs. How you will contribute Supports all local Manufacturing Plasma Operations. Submit safety related beacons as necessary. Update shipping and receiving metrics daily. Receives physical and electronic plasma shipments. Ship and receive bulk albumin, raw materials, and finished goods. Performs order status inquiries for all completed orders. Adjusts orders as necessary...

Prin Clinical Research Spec – Surgical Robotics Operating Unit The Principal Clinical Research Spec is responsible for developing strategies and driving processes to meet the milestones of complex clinical studies/projects in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs. This role utilizes their broad range of experience in managing the technical execution of the trial and manages trials of a higher degree of complexity and global nature. This role works independently and under only general direction. Major deliverables are reviewed to ensure clinical and business requirements are met. The position provides work direction and...

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 Program Manager, you will have primary responsibility of managing the integrated clinical and medical science strategy for the Esophageal and Gastric portfolio. You will lead clinical evidence generation and dissemination and collaborate across the organization to drive market adoption for multiple innovations across the portfolio. This position should be able to function with minimal supervision. As an...

Medtronic is hiring in our Memphis Airways Distribution Center, here our employees are helping us deliver on the extraordinary. We require fresh ideas and inclusive insights to maintain our position as an innovative industry leader. That’s why we actively seek, attract, and develop employees who are patient-centric, passionate, and who reflect the wide variety of life experiences found among our patients. We’ve been on a three-year journey to modernize our U.S. distribution network and transform how we distribute our products. We’re aiming to elevate the customer experience and generate cost savings with state-of-the-art technology and standardized processes. But none of...

We are excited to have a Cardiac Echo Sonographer with experience in Structural Heart join our team as a Senior Clinical Research Specialist! Are you passionate, self-motivated and looking for a new challenge? Join Medtronic Structural Heart and Aortic team that works with Mitral and Tricuspid team creating superior therapies for patients with Mitral and Tricuspid Valve Disease. Careers That Change Lives In this exciting role as a Cardiac Echo Sonographer (Senior Clinical Research Specialist), you will play a critical role in enhancing the quality, safety, and efficacy of clinical research. Your responsibilities will include providing expert echocardiography and imaging...

This is a Remote Based position. Candidate must be located near an airport (Texas, Louisiana, Arizona, Arkansas, Oklahoma, Florida - highly desirable locations). The successful candidate will be required to travel up to 80% of the time. The Senior CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Pharma clinical trials within the country. The Senior CRA is responsible to deliver data within timelines and required quality standard, and adherence to monitoring procedures in accordance with ICH/GCP and US CFR and company SOPs. LI-#Remote This position can be based remotely anywhere...

The Coordinator, Oncology Planning & Execution responsibilities include working closely with Head of Oncology Planning and Execution and team and r espective Oncology leadership team members to perform numerous and varied tasks, such as engaging within internal and external stakeholders, coordinating bi-yearly Scientific Advisory Forum and advisory boards, external engagement activities, internal and external Governance and Board meetings (including assisting with preparations for board meetings, external partner meetings, interactions, and scientific engagements). In addition, the Oncology Development Coordinator will perform administrative duties, scheduling support and coordination of future internal and external audits, coordinating recruitment and onboarding activities, handling financial queries...

The Team Coordinator provides comprehensive administrative and operational support to ensure the effective functioning of the Sanofi Integrated Launch Capabilities (SILC) team. This role serves as a key point of contact, coordinating activities, managing communications, and supporting team initiatives to drive efficiency and productivity. We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing...

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 to drive procedural and practice success. Technical and Clinical Support 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 consistency and best...

Jenny was promoted to FCL - replacing her role in Miami 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...

This position works out of our Plymouth, MN location in the EP division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. As the Senior Contract Coordinator, you'll have the chance to w ork cross-functionally to facilitate contracting with health care providers (HCP) to support the organization's operational needs. Perform a variety of specialized contract management activities to ensure the organization's agreements are legally sound, protect its business interests, and comply with all relevant laws and regulations. What...

In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises independent judgment in planning,...

Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as the Director, Clinical Trial Reporting based remotely reporting to the VP, Clinical Data Operations & Standards. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by...

Sarepta Therapeutics is seeking a motivated Research Associate II ideally with experience working in a GCP/GLP environment for a clinical research operations support role. This position will collaborate with both internal and external stakeholders in planning, execution, and management of clinical sample logistics and clinical trial operations with a focus on specialty labs, biomarker, and immunology sample testing. This position will support site training, site feasibility activities, and oversight related to the transfer of samples from collaborators, vendors and CROs to Sarepta and third-party facilities. Working closely with the clinical operations, data management, translational, biomarker, and immunology R&D teams, this...

Clinical Study Monitor – Companion Diagnostics (CDx) The Clinical Study Monitor – Companion Diagnostics (CDx) is responsible for overseeing the day-to-day execution and monitoring of clinical studies involving in vitro diagnostic (IVD) devices, with a focus on companion diagnostics developed in collaboration with pharmaceutical and consortia partners. This role ensures that clinical performance studies are conducted in accordance with the protocol, applicable regulations (e.g., IVDR, GCP, FDA), and company SOPs. The Study Monitor will work closely with cross-functional teams including study team members, Quality and Clinical Affairs to support study site compliance and data quality. This position is ideal...

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 to drive procedural and practice success. Technical and Clinical Support 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 consistency and best...

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. Trial Capabilities Associate (P1-P3-2) Purpose The Trial Capabilities Associate (TCA) provides...

The Sr. Clinical Director for Neuromodulation, Pain Therapies reports to the VP, Clinical Research and Medical Science NMPH. This position is responsible for directing all global clinical research activities and programs to generate clinical evidence in support of the business. The Sr. Clinical Director is responsible for supporting the clinical strategy in alignment with the business, R&D, regulatory and commercial strategies for the pain therapies business. The leader is also responsible for designing and driving the execution of pre-market and post-market clinical trials globally, including driving outcomes and results, and collaborating for the dissemination of the resulting evidence to internal...

Associate Director, Clinical Research, Value & Evidence Generation, US Medical Lexington, MA Hybrid OBJECTIVES/PURPOSE Provides clinical project management and leadership to ensure successful operational execution of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS) collaborative studies and Investigator Initiated Research (IIR). Specific objectives include Partners with Head of US Medical Clinical Science Lead to translate strategy into efficiently executable research plan; predicting and planning solutions to achieve successful operational execution to meet study objectives and strategic objectives; driving the team to achieve clarity on issues and focus on effective contingencies; interfacing with senior management and influencing...

About the role As a member of Takeda Oncology, your work will contribute to our bold, inspiring vision We aspire to cure cancer. Here, you'll build a career grounded in purpose and be empowered to deliver your best. As part of the Global Medical Affairs Oncology Evidence Generation team, you will report to the Lung Evidence Generation Lead/ Medical Affairs Company Sponsored (MACS) Program Leader and work with various departments and functions. How you will contribute Assists with study tasks under the supervision of Investigator-Initiated Research (IIR), Externally Sponsored Collaborative Research, and MACS Study Leads Works closely with field staff,...

Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Senior Director, Clinical Trial Configuration based in Cambridge, MA reporting to the VP, Clinical Data Operations & Standards . At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global...

Johnson & Johnson MedTech Orthopaedics is recruiting for a Senior Coordinator, Education Logistics – located in Colorado Springs, Colorado. About Orthopaedics 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 Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities,...

Careers That Change Lives In this exciting role as SH&A R&D Project Coordinator IV for the Mounds View, Minnesota campus, you will be supporting the on-site R&D team activities. Specifically, you will be supporting the TAVR & Congenital R&D, Project Management Office, and Modeling, Simulation, and Reliability leadership teams. This includes coordinating on-site meetings, driving leadership team action items, supporting team leaders with purchase orders, calendars, travel arrangements, and meeting logistics. Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. It’s no accident — we work hard...

This is a Remote Based position. Candidates must be located near an airport (California, Washington, Oregon, Montana, Nevada, Idaho- highly desirable locations). The successful candidate will be required to travel up to 80% of the time. The Senior CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Pharma clinical trials within the country. The Senior CRA is responsible to deliver data within timelines and required quality standard, and adherence to monitoring procedures in accordance with ICH/GCP and US CFR and company SOPs. LI-#Remote This position can be based remotely anywhere in...

Responsibilities may include the following and other duties may be assigned. Maintains schedules for equipment spare part/supplies/tools ordering and availability for the maintaining of industrial and commercial manufacturing equipment to support maintenance efforts. Compiles records concerning quantity, cost, and type of spare parts/supplies/tools received, shipped, in stock or inventory, and/or in production. Expedites flow of parts/supplies/tools within or between departments in accordance with production and shipping schedules. Determine alternative spare parts/supplies for cost savings or improved reliability. Assists in determining possible and actual part shortages. May initiate action to correct these deficiencies. Uses knowledge of production, procurement, and engineering departments...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

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 position is not remote, it is located on site in Sierra Vista, AZ** PRIMARY RESPONSIBILITIES Split clinical and administrative duties Patient communications, including draw and timing requirements. Administrative duties, such as accessing patient information and reports in Electronic Medical Record (EMR), scheduling patients, aligning available blood draw times to clinic requirements, etc. Work from home time to be noted on timecard, submitted weekly Requires tracking and data entry for each drawcompleted,...

Are you passionate about talent acquisition and ready to make a real impact in a dynamic, fast-paced environment? Neurocrine Biosciences is seeking a Sr. Talent Acquisition Coordinator in San Diego to play a pivotal role in our Talent Acquisition (TA) team. This is your chance to contribute to the recruiting process, enhance candidate experience, and ensure our recruiting systems and programs scale to meet our future growth. _ Your Contributions (include, but are not limited to) Heavy coordination and scheduling of complex Clinical interviews for candidates across various departments, ensuring timely communication and logistical arrangements Handle travel and expense reporting,...

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 GI Therapeutic Area within Lilly Immunology Development is focused on...

Clinical Research Medical Director – Hematology Oncology What you will do In this vital role you will have an opportunity to shape this Therapeutic Area. This role will report directly to the Global Development Lead for a program. The position may be in-person or remote. Provide therapeutic area expertise in prostate cancer and contribute to the development, execution, and communication of the global scientific/medical evidence plan for hematology-oncology Serve as the medical monitor on key clinical trials in prostate cancer Conduct medical review of clinical trial data Support cross-functional and global collaborations to integrate broad medical, scientific, and commercial...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

Our location Lake Forest, IL has an opening a Project Coordinator position. This person will be responsible to manage the development and implementation process of the company's products and services involving departmental or cross-functional teams focused on the delivery of new or existing products. What You’ll Work On Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort. Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to...

In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises independent judgment in planning,...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

Head of Precision Medicine Program Management What you will do In this vital role you will lead a group of PMs to drive and develop global strategic Precision Medicine Plans for programs within Amgen’s Precision Medicine. The Director of the Program Management Office (PMO) in Precision Medicine partners with cross-functional stakeholders and manages Sr. PMs across all TAs in Research and Development to drive the creation and effective, consistent completion of high-quality, cross-functional, strategic precision medicine plans for Amgen’s assets. The Director also supports strategic cross-functional initiatives across Precision Medicine and key partner functions internal and external to Amgen....

Sr Inventory Coordinator This position works out of our Altavista, VA location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. Altavista, Va. , is one of Abbott’s largest nutrition manufacturing plants equipped with advanced technology to ensure efficient production. Working here will make you...

This position works out of our Alameda, CA location in the Diabetes Care division where we're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. This is an on-site position in Alameda, California. This is not a remote position. What You’ll Work On The...

This position works out of our Alameda, CA location in the Diabetes Care division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. As a Coordinator Project Design, you will have the opportunity to provide organizational and project support to the department by working directly with a cross-functional teams, external translation suppliers, as well as internal Design Production Artists to coordinate and execute activities related to the development of packaging and labeling...

About This Role Make the most meaningful impact of your career in this rewarding role with Biogen, a well established pioneer in the pharmaceutical industry. This is your rare opportunity to transcend day-to-day management operations as you design operational strategy and oversee our clinical research organization (CRO) partners to develop clear protocol concepts and final protocols. The best part You will own responsibility for entire clinical trial studies, including operational design, successful delivery, and the positive impact on the lives of patients with a wide array of conditions, including nephrotic conditions, multiple sclerosis (MS), Alzheimer’s disease, and spinal muscular atrophy...

Patent Coordinator What you will do Amgen is searching for a Patent Coordinator – Biotechnology & Process Development in our Intellectual Property and Litigation group. This role can be based at Amgen’s headquarters in Thousand Oaks, California; Amgen's site in Cambridge, Massachusetts; or at Amgen’s site in South San Francisco, California. Also considering remote workers outside a commuting distance from the listed locations. The successful candidate will provide support to the Intellectual Property Law team by assisting with the preparation, filing (including e-filing), prosecution, and maintenance of patent applications both U.S. and Foreign. Candidate may prepare interference and opposition...

Your skills could be critical in helping our teams accelerate progress. 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, and to incorporate new methodologies and pro-actively progress study execution. We are an innovative global healthcare company with one purpose to chase the miracles of science to improve people’s lives. We’re also a company where you can...

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. *This is not a remote position and will...

Johnson & Johnson is hiring for a Clinical Research Manager - Shockwave Medical (Remote) to join our team. The position is FULLY REMOTE and can sit anywhere in the US . 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...

Johnson & Johnson is hiring for a Principal Clinical Research Associate – Shockwave Medica l (Remote) to join our team. 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 by innovation at...

Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases. Immunovant is seeking a Senior Clinical Trial Manager to play a key role on a highly dynamic, cross-functional team. Reporting to the Director, Clinical Operations, you will be responsible for supporting the advancement of rare disease clinical trials as part of Immunovant’s Clinical Operations Team. Key Responsibilities Lead Study Start-up activities, including but not limited to...

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...

The Director (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 Director will manage the entire cycle of clinical development for late-stage studies, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, The Director May Be Responsible For Planning clinical trials (design, operational plans, settings) based on these clinical development strategies Monitoring and managing the conduct of ongoing or new clinical...

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Twist Bioscience is looking for a seasoned, team-oriented, Shipping Coordinator. This position will play a critical role in forming a best in class Shipping/Order Fulfillment team. This position will require collaboration with Manufacturing, Customer Support, and Supply Chain teams to ensure internal and external customer satisfaction. The Shipping Coordinator will perform all physical and administrative required for this position. This will include inventory management, continuous improvement, shipping, receiving, storing, distributing of orders, materials, parts, supplies and equipment. Must possess a team and collaborative attitude. Responsibilities Order fulfillment Perform inventory audit, reconciliation and inspection of finished goods and raw material.. Monitor,...

*** This is an in-clinic position in Cody, WY *** 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. PRIMARY RESPONSIBILITIES Split clinical and administrative duties Patient communications, including draw and timing requirements. Administrative duties, such as accessing patient information and reports in Electronic Medical Record (EMR), scheduling patients, aligning available blood draw times to clinic requirements, etc. Work from home time to be noted on timecard, submitted weekly Requires tracking and data entry for each drawcompleted, including billing information when...

POSITION SUMMARY The Senior Clinical Trial Manager (CTM) will be responsible for managing all aspects of clinical trials from start-up through close-out. The Sr. CTM should have experience in managing all aspects of the trials independently. The Sr CTM is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements. The Senior Clinical Trial is responsible for complex studies and has the experience, skills and knowledge to work independently. PRIMARY RESPONSIBILITIES Manage the execution and conduct of...

Children’s Medical Center Research Institute at UT Southwestern (CRI) is a joint venture established in 2011 to build upon the scientific excellence of UT Southwestern Medical Center and the clinical expertise of Children’s Medical Center. CRI’s mission is to perform transformative biomedical research to better understand the biological basis of disease, seeking breakthroughs that can yield new strategies for treating disease. CRI is creating interdisciplinary groups of scientists and physicians to pursue research at the interface of regenerative medicine, cancer biology, and metabolism, fields that hold uncommon potential for advancing science and medicine. We are seeking an Administrative Coordinator to...

The Office Services Coordinator role involves managing various aspects of office operations, such as space planning, office supply purchases, inventory control for breakrooms and workrooms, overseeing vendor services, mail sorting, and maintaining office signage. The ideal candidate should possess strong organizational skills, attention to detail, and effective multitasking abilities. _ Your Contributions Assist with space planning and updating floor plans as needed Oversee office supply purchases and pricing and manage inventory levels Developing standards and Inventory control for the breakroom and workrooms Manage Corodata (shredding services) vendor for secure disposal of sensitive information services and invoicing for all services Sort...

Clinical Research Associate (CRA), Oncology, As a Field Based Clinical Research Associate , you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. In this role as an Oncology CRA , you will have the local responsibility for the delivery of the studies at allocated centers and are active participants in the local study team(s). You’ll work in close collaboration with other Monitors and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will also be responsible for...

Johnson & Johnson is hiring for a Sr . Clinical Research Associate - Shockwave Medical (Remote) to join our team. The position is FULLY REMOTE and can sit anywhere in the US. 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...

Clinical Research Medical Director – Small Cell Lung Cancer What you will do In this vital role you will have an opportunity to shape this Therapeutic Area. This role will report directly to the Global Development Lead for a program. The position may be in-person or remote. Provide therapeutic area expertise in thoracic oncology and contribute to the development, execution, and communication of the global scientific/medical evidence plan for small cell lung cancer area. Serve as the medical monitor on key clinical trials in prostate cancer Conduct medical review of clinical trial data Support cross-functional and global collaborations to...