- IQVIA (Durham, NC)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (Durham, NC)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (Durham, NC)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Durham, NC)
- **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will ... **Why Join Us?** Be part of a team that's driving innovation in clinical research . Your contributions will help shape the future of healthcare. Apply now and… more
- IQVIA (Durham, NC)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate , you...research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent ... regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research 's applicable SOPs and working practices....is provided to the Field Monitor from the assigned Clinical Trial Associate . + Works closely with… more
- J&J Family of Companies (Raleigh, NC)
- Sr Clinical Research Associate - 2406209639W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation ... & Johnson Medtech companies is recruiting for a Sr Clinical Research Associate , located anywhere...+ Conduct site initiation visits; train site personnel on sponsor and regulatory requirements for study conduct; participate in… more
- Allucent (Cary, NC)
- …life-changing therapies to patients in need across the globe. We are looking for a Sr. Clinical Research Associate (sCRA I) to join our A-team (remote, with ... and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in… more
- IQVIA (Durham, NC)
- IQVIA MedTech is seeking a Clinical Research Associate II with Medical Device monitoring experience! Central Nervous System (CNS) experience is a plus! Job ... on-site monitoring experience + Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice… more
- UNC Health Care (Chapel Hill, NC)
- …and external stakeholders, including University research office personnel, clinical faculty and staff, faculty investigators, and sponsor representatives, ... serve. **Summary:** The Department of Pediatrics is seeking an experienced clinical Research Administrator for the Department's centralized administrative core.… more
- United Therapeutics (Durham, NC)
- … clinical trial material (CTM) is available for sites and/or Contract Research Organizations (CRO); Lead final clinical study report writing to summarize ... company experience in clinical development with a PhD/PharmD + For ( Clinical ) Product Development Associate Director level: + Master's degree or +… more
- Institute for Medical Research (Durham, NC)
- …to oversee study personnel, implementation, and quality assurance in support of clinical research studies conducted by the Principal Investigator, Dr. Stephen ... support personnel, facilitating manuscript development, ensuring quality of clinical research documentation, assisting in implementation of study-related… more
- Medtronic (Raleigh, NC)
- …procedures including TMVR or LAAC or other adjacent therapies + Clinical Research experience including coordinating multi-center trials and/or significant ... group presentations and hands-on experience with interventional/surgical cardiac procedures + Clinical Research experience in structural heart or other medical… more
- Institute for Medical Research (Durham, NC)
- …skilled in customer service and/or relations, and who may have an interest in clinical research . The successful candidate will be employed in the laboratory of ... of research study participants and implementation and execution of several clinical research projects, which may also include the acquisition and maintenance… more