Research Engineer I, Milwaukee

Payrate: $40.00 - $40.00/hr.

 

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. 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:

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, My Workshop, 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).

 

 

Pay Transparency: The typical base pay for this role across the U.S. is: $40.00 - $40.00/hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.

 

For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy ((url removed)).

 

Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process.  AI technology is used to gather data only and does not replace human-based decision making in employment decisions.  By applying for this position, you agree to Aditi’s use of AI technology, including calls from an AI Voice Recruiter.

 

#AditiConsulting