Clinical Study Project Manager

February 15

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Infotree Global Solutions

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Infotree Global Solutions is a staffing and workforce management company that aims to meet the career needs of individuals while ensuring client satisfaction through its resources. It is heavily focused on recruitment and consultant care, providing opportunities across various industries such as automotive, engineering, IT, finance, and banking. Founded in 2002, Infotree Global Solutions operates globally, with more than 5,000 coworkers and 400 recruiters in 150 countries. The company is committed to delivering quality placements that lead to lifelong careers, supported by a dedicated team of recruiters and consultant care representatives.

Contract Staffing • Permanent Placement • Independent Contractor Solutions • Statement Of Work • Global Employer of Record

1001 - 5000 employees

Founded 2002

🎯 Recruitment

👥 HR Tech

🏢 Enterprise

📋 Description

• As a Clinical Study Project Manager, you will be responsible for end-to-end management of clinical studies, overseeing the process from initial planning to completion. • Your key duties will include: Selecting, negotiating, and contracting clinical study vendors. • Leading tenders preparation and execution with external consulting partners. • Developing study-related documents in collaboration with internal teams and contracted CROs. • Participating in feasibility and site selection processes for clinical studies. • Creating and overseeing the recruitment strategy, ensuring studies meet required participant numbers. • Acting as the main point of contact, leading and managing studies from start-up to close-out. • Coordinating with internal and external stakeholders to ensure timely execution and budget control. • Supporting quality assurance process implementation for clinical and medical research activities.

🎯 Requirements

• Master’s degree in a science/health-related field. • Project management experience in multi-center clinical studies (minimum 3 years). • Experience in at least one of the following areas: Full-cycle project management in multi-center clinical studies (from start-up to close-out). • Start-up phase project management in multi-center clinical studies. • Working knowledge of Good Clinical Practice (GCP). • Strong communication, collaboration, and leadership skills. • Excellent problem-solving and planning abilities. • Ability to work independently and within set timelines. • Fluent English skills (verbal and written). • Proficiency in clinical study management tools and software.

🏖️ Benefits

• Flexible working environment • Engaging and impactful projects • Career growth opportunities • Work with leading experts in the field