Clinical Project Manager

Integrated Resources INC

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South Plainfield, NJ, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

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.

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.

Kind Regards,

Kavita Kumari

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - 732-844-8726

About this role

Summary

Manage clinical trial activities, oversee project lifecycle, ensure compliance with regulations.

Job title

Clinical Project Manager

Experience level

5+ years

Industry

healthcare

Location requirements

On-site in South Plainfield, NJ, no remote work allowed.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

clinical trialsproject managementFDA regulationsGCP/ICHdrug development

Preferred skills

hematologyoncologyCRA experience

Specializations

clinical trialsdrug developmentoncologypharmacology
Locations

Structured locations inferred from the posting.

South Plainfield, NJ 07080, USA

On-site City