- Merck & Co. (Rahway, NJ)
- Job DescriptionThe primary function of the Clinical Research Associate (CRA) I position is to assist with clinical study operations as well as monitor ... will be conducted in compliance with the requirements of Good Clinical Practice (GCP).The Clinical Research Associate I acts as a point of contact with… more
- Merck & Co. (Rahway, NJ)
- …MS Excel and WordPreferred Experience and Skills: Strong preference for experience with clinical trial specialty servicesExperience, either at a sponsor or CRO, ... Job DescriptionThe Associate Director is responsible for defining sourcing strategies... Director is responsible for defining sourcing strategies for Clinical Innovative and Decentralized Services in support of our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: Responsibility for ... study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready...related to CDx for Health Authority interactions (for both sponsor and partner side) CDx RA Policy and Intelligence… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …according to local requirement. **MINIMUM RECRUITMENT STANDARDS:** + **2.5 years of clinical research coordination experience at site level** + Nursing or ... of education, training and experience IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… 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 ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- IQVIA (Parsippany, NJ)
- …is required, Nursing experience in addition to this is ideal!_ **Job Overview** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an integral ... of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws, regulations and… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Nurse is a Registered Professional Nurse who is responsible for assisting in the assessment, management, and ... coordination of care for subjects enrolled onto IRB approved research studies/ clinical trials, as specified by the research protocol, across the continuum of… more
- Research Foundation CUNY (New York, NY)
- Job Title: Director of Clinical Healthcare Programs PVN ID: LA-2507-006906 Category: Instruction and Social Service Location: LAGUARDIA C. C. Job Description General ... to the Senior Director of Workforce Development, the Director of Clinical Healthcare Programs develops, implements, manages, assesses, and improves industry-informed… more
- IQVIA (Parsippany, NJ)
- …materials as required. Qualifications * Bachelor's Degree Related field. * 3-5-year relevant sponsor or clinical research organization clinical site ... language, terms, and financial options. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- CVS Health (Trenton, NJ)
- …solving issues. + Utilizes ATV/Med Compass, ASD and other Aetna systems to research and enter member benefit plan information. + Responsible for initial review and ... in accordance with the benefit plan information. + Performs non-medical research including eligibility verification, COB, and benefits verification. + Promotes… more
