- IQVIA (Durham, NC)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… 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
- Parexel (Raleigh, NC)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
- Parexel (Raleigh, NC)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... local country regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) +… more
- Parexel (Raleigh, NC)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery ... associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of… more
- Parexel (Raleigh, NC)
- …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global...of the projects according to contracted agreement with the sponsor (ie: tasks and time per task contracted) and… more
- ICON Clinical Research (NC)
- …Based (San Diego, CA) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ... us on our mission to shape the future of clinical development. **Study Start Up Associate II**...field. + Minimum of 2 years of experience in clinical research or regulatory affairs, with specific… more
- IQVIA (Durham, NC)
- …IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates ... ** Associate Director, Client Services - Clinical ...mid-size environment is highly preferred. + Experience in the Clinical Research industry is highly preferred. +… more
- WCG Clinical (Cary, NC)
- …in clinical strategy, data analytics, site identification or feasibility at a sponsor or clinical research organization. + Demonstrated ability to ... with product management in developing digital solutions or analytics platforms for clinical research or hospital/healthcare settings. + Minimum of 8 years'… more
- ThermoFisher Scientific (Greenville, NC)
- …management and oversight of all contracted services. **Discover Impactful Work:** The Associate /Medical Director provides medical oversight of clinical trials to ... with the applicant's training (comparable to 2 years); Or + Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company… more