Clinical Project Manager

Integrated Resources, Inc

South Plainfield, New Jersey

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JOB DETAILS

JOB TYPE

Full-time

SKILLS

Biology, Biotech and Pharmaceutical, Clinical Trial, Clinical Trial Management, Contract Research Organization (CRO), Drug Development, Financial Management, Hematology, Hospital, Oncology, Phase I Clinical Trials, Phase III Clinical Trials, Project/Program Management, Team Lead/Manager

LOCATION

South Plainfield, New Jersey

POSTED

2 days ago

Clinical Project ManagerThe Clinical Program Manager reports to the Program Director and Clinical Operations Group Leader. The Clinical Program manager is the first-line administrator within the Clinical Operations group responsible for the planning, implementation, coordination, supervision and execution of assigned Clinical Trial(s) activities throughout the entire lifecycle.Bachelor's degree, preferably in the life science or related field, advanced degree preferred. 5+ years or relevant project management of clinical trials experience managing all aspects of a Clinical Project to include financial management, drug development/NDA process, study development and implementation in a CRO and/or pharmaceutical industry with a focus on hospital-related drugs. 3+ years of experience as a CRA in Phase I-III clinical trials. Hematology/Oncology experience (highly desired but not required). Demonstrated comprehensive experience in clinical research processes, FDA regulations and GCP/ICH guidelines.

About the Company

Integrated Resources, Inc

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Clinical Project Manager

Integrated Resources, Inc

South Plainfield, New Jersey

About the Company

Integrated Resources, Inc

Resume Resources

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