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Clinical Project Manager

2 hours, 25 minutes ago
Serbia
Full-time
Senior
Project Manager
Project and Program Management
GCP
Apply Now
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised
View All Jobs 114

Description

  • Lead full-service clinical projects in line with study budget, scope of work, timelines, and quality expectations.
  • Serve as the primary client liaison and provide customer service throughout the project lifecycle.
  • Participate in proposal strategy, development, costing, bid defense, and client presentations.
  • Manage all aspects of one or more clinical research trials, including cross-functional coordination.
  • Oversee functional areas such as data management, safety, clinical, medical monitoring, and biostatistics.
  • Prepare project status updates for clients and internal management, including deliverables, performance metrics, and escalations.
  • Review and prepare protocols and study documents, including project plans, informed consents, site contracts, and budgets.
  • Work with internal and external stakeholders, including project teams and senior management up to C-level.
  • Coordinate and support efficient study execution across global and international trials.
  • Manage client relationships, project teams, budgets, and timelines through the full study cycle.

Requirements

  • Degree or equivalent related life science qualification, or a comparable combination of education and experience.
  • 5 to 7 years of industry experience and at least 4 years of full-service project management experience in a clinical trial setting.
  • Prior full-service or global Project Management experience in the CRO industry is essential.
  • Experience managing oncology studies is required.
  • Working knowledge of GCP/ICH guidelines and the clinical development process.
  • Ability to travel domestically and internationally, including overnight stays.
  • Strong written and spoken English communication skills.
  • Strong presentation skills.
  • Proficiency with MS Office, MS Project, and PowerPoint.
  • Experience with CTMS, eTMF, EDC, and IXRS software systems.
  • Ability to build positive working relationships with internal and external teams.
  • Core understanding of medical terminology and clinical trial activities related to clinical development planning.

Benefits

  • Supportive, collaborative team environment.
  • Work-life balance focus.
  • Opportunities for team development.
  • High-energy, dynamic work environment.
  • Exposure to innovative oncology and precision medicine programs.
  • Equal Opportunity Employer protections and accommodations for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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