Clinical Project Manager

Immediate need for a talented Clinical Project Manager. This is a 06+months contract opportunity with long-term potential and is located in Wauwatosa, WI (Hybrid). Please review the job description below and contact me ASAP if you are interested.
 
Job ID:25-71201
 
Pay Range: $39 - $40/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan .
 
Key Responsibilities:

• Project Execution:
• Manage internal and external research activities, including Client - 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.

Key Requirements and Technology Experience:

• Key Skills: Clinical Project Manager, Good Clinical Practices (GCP), Medical device/Pharma .
• 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).

Our client is a leading Electrical Logistics Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
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