- 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
- IQVIA (Durham, NC)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ... expectations. Your work will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct all types of site… 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
- Actalent (Chapel Hill, NC)
- …team dedicated to advancing groundbreaking clinical research . As a Research Proposal Development Associate II, you will contribute to the development and ... Job Title: Research Proposal Development Associate II Job...Engage in meaningful work within the world's largest academic clinical research organization, benefiting from professional growth… 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