- Merck & Co. (Rahway, NJ)
- …and education activities supporting the monitoring roles in clinical operations eg - Clinical Research Associate (CRAs), Clinical Research ... (eg, master's degree, MD, PhD) Required -Experience: - 5 years of experience in clinical research , with mandatory 2 years of CRA experience. - 6 months of… more
- Parexel (Trenton, NJ)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned ... Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and monitoring, managing...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
- Parexel (Trenton, NJ)
- …positions- Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate ( CRA ) has local responsibility for ... an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and...audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in ... studies. The SrCSA performs all the duties of the CRA with higher proficiency, independency, accountability, and ability to...audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable for site management and monitoring, managing...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... Whether you're beginning or continuing your career as a CRA , this role is an ideal stepping-stone. You'll have...three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. +… more
- IQVIA (Parsippany, NJ)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred: + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of positive change. The ** Clinical Research Nurse** is responsible for coordinating...to March 31, 2024 require a minimum of an associate in Nursing or diploma of Nursing degree.) Note:… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred:** + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of positive change. The ** Clinical Research Nurse** is responsible for coordinating...to March 31, 2024 require a minimum of an associate in Nursing or diploma of Nursing degree.) +… more
- Hackensack Meridian Health (Paramus, NJ)
- …Preferred** : + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of positive change. The ** Clinical Research Nurse** is responsible for coordinating...to March 31, 2024 require a minimum of an associate in Nursing or diploma of Nursing degree.) +… more
