Deliverables: Provide local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Operational oversight of assigned projects at the country level for end-to-end project management from start-up through to closeout activities. Ensure the local trial t
Role Summary The Clinical Trial Transparency and Disclosure Lead is an integral member of the Medical Writing department. The role is responsible for providing strategic and operational expertise to support the disclosure of clinical regulatory documents pertaining to Pfizer-sponsored interventional
Department: 38923 Wake Forest University Health Sciences - Gerontology Status: Part time Benefits Eligible: Yes Hou rs Per Week: 29 Schedule Details/Additional Information: Up to 29 hours/week, on-site Pay Range $24.10 - $36.15 JOB SUMMARY This is an on site role within the Alzheimer's Disease Resea
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 co
Title: Clinical Research Associate *This role is located in either New York or New Jersey The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration wi
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and ma
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, in
Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Clinical Project Manager is an essential member of the core project team responsible for project delivery of clinical stu
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in differ
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU)
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
Job Description 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
Job Description The Clinical Research Director (CRD) is the Clinical Operations lead in a country/cluster and is responsible for execution of all Clinical Trials in scope for GCTO country operations. Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection ready
Job Description The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensu
Overview: M-F schedule, remote one day per week dependent on patient visits, and rare but possible Saturday and Sunday patient visit (minimal, 2-3 hours; based on study assignment). Job Description Summary: Works with the study physician to ensure all patients involved in a clinical research trial a
Overview: Job Description Summary: Manages elements of a clinical study to meet protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures. Coordinates start-up activities, launch activities, day-to-day management of a study, and study closur
Position: Digital Proxy Product Owner – Clinical Trials Risk Based Quality Management. Location: Hyderabad This job offer is accessible to all, regardless of gender. About the job At Sanofi, we chase the miracles of science to improve people’s lives. Digital R&D’s mission is to bring the power of tr
Work Schedule Other Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Australia and New Zealand Candidates are welcome to apply Relocation support to Brisbane may be provided for the successful candidate Location: Brisbane, Australia (Home-based, 100% Remote) Employment Type: Full-time At
Job Description Department of Emergency Medicine has an outstanding opportunity for a Research Study Coordinator 1. About this Opportunity: Report to Research Coordinator 4, the Research Study Coordinator 1 will coordinate and perform work in support of clinical and health services research in EMS.
At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to fo
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher’s PPD clinical research business, we’re using digital innovation, data science, and AI to reimagine how life-changing therapies reach patients. Our teams combine deep scientific expertise with advanced
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 bioteches, spanning 2,700 clinical trials acro
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakt