Clinical Research Project Manager

Integrated Resources, Inc ( IRI ); Wauwatosa (WI); Hybrid; USD 80,000 - 100,000; Full time

Job summary

A leading company is seeking a Clinical Research Project Manager to oversee research activities in the Advanced Visualization Solutions business. This hybrid role requires managing research projects, ensuring compliance, and fostering relationships with partners. The ideal candidate will have a strong background in clinical research and project management, along with a relevant degree. This position offers a competitive pay rate and the opportunity to work in a dynamic environment.

Qualifications

• Progressive experience in project management of clinical or technical research.
• Strong understanding of Good Clinical Practices (GCP).

Responsibilities

• Manage internal and external research activities.
• Ensure compliance with research standards and regulations.
• Negotiate budgets and contracts with external partners.

Skills

Project Management

Clinical Research

Compliance

Education

Bachelor’s degree in life sciences

Master’s degree in a scientific field

Job description

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Integrated Resources, Inc ( IRI ) provided pay range

This range is provided by Integrated Resources, Inc ( IRI ). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $40.00/hr

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Lead Recruiter at Integrated Resources, Inc ( IRI )

Title- Clinical Research Project Manager

Duration: 6 months+

Note - this is a hybrid role that is 3 days a week in office at address below and 2 days remote. Please submit local candidates to the address below only.

Job Description Summary

The Clinical Research Project Manager (Research Program Integrator – RPI) is responsible for leading and managing defined research activities for the Advanced Visualization Solutions (AVS) business within Client HealthCare. This role oversees cross-functional planning, execution, and communication to ensure timely, high-quality, and compliant delivery of research projects. The RPI manages the full lifecycle of research initiatives—from strategic planning through execution and closure—while meeting all quality, content, schedule, and budget targets.

Roles and Responsibilities

Project Execution

- Manage internal and external research activities, including GEHC- and Investigator-Sponsored Studies, product evaluations, reader studies, and other strategic research initiatives.

- Lead cross-functional teams to execute research projects in alignment with business needs and study plans.

- Partner with the Research Manager (RM) to prioritize and adjust study details as needed.

Compliance & Documentation

- Ensure all research activities comply with cross-functional standards, Phased Review Discipline, QMS, SOPs, GCP, and applicable regional regulatory requirements.

- Develop and manage essential research documents, including protocols, study plans, informed consent forms, and document storage.

- Maintain accurate and timely study records in systems such as Clinical Trials Management System, MyWorkshop, ClinicalTrials.gov, Support Central, and others.

Stakeholder & Site Management

- Negotiate budgets and contracts with external partners and manage payment processes.

- Conduct or coordinate training, site initiation, monitoring, and study closure activities.

- Serve as a quality control reviewer for peer studies, supporting review and approval of study activities.

- Build and maintain professional, productive relationships with external research partners and study sites.

Required Qualifications

- Bachelor’s degree in life sciences, engineering, clinical field, or equivalent.

- Demonstrated progressive experience in project management of clinical or technical research in a clinical setting, industry, government agency, or a similar role in a medical device or pharmaceutical company.

- Strong understanding of Good Clinical Practices (GCP) and global/regional research or device regulations.

- Proven ability to build and sustain cross-functional relationships.

Desired Characteristics

- Master’s degree in a scientific or related field, or an advanced medical degree.

- Professional certification in project management (e.g., PMP) or clinical research (e.g., CCRP, CCRA, CCRN).

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Other

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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Clinical Research Project Manager - Hybrid

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