Clinical Project Manager
Integrated Resources INC
South Plainfield, NJFull-time
Behavioral Health Market Context
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Job Description
dily grow.
Job Description
The 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.
Qualifications
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.
Additional Information
Kind Regards,
Kavita Kumari
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
DIRECT # - 732-844-8726
Job Description
The 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.
Qualifications
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.
Additional Information
Kind Regards,
Kavita Kumari
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
DIRECT # - 732-844-8726
Qualifications
- •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
- •Demonstrated comprehensive experience in clinical research processes, FDA regulations and GCP/ICH guidelines
Benefits
Responsibilities
- •The 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
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