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Clinical Project Manager

3 days, 6 hours ago
Spain
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 102

Description

  • Lead full-service clinical projects in line with study budget, scope of work, timelines, and quality standards.
  • Serve as the primary client point of contact and support proposal activities and client presentations.
  • Liaise with project teams and senior management at Precision and sponsor organizations, including executive-level stakeholders.
  • Oversee all aspects of clinical research trials across functional areas including data management, safety, clinical operations, medical monitoring, and biostatistics.
  • Prepare project status updates for clients and management, including key deliverables, performance metrics, and escalation items.
  • Participate in proposal strategy, development, costing, and bid defense activities.
  • Review and prepare study documents such as protocols, project plans, informed consents, site contracts, and budgets.
  • Manage client relationships, project teams, and budgets throughout the full study lifecycle.
  • Coordinate cross-functional trial execution and drive efficient study delivery across internal and external stakeholders.

Requirements

  • Degree in a life science field or an equivalent combination of education and experience.
  • 5 to 7 years of industry experience, including at least 4 years of full-service project management experience in a clinical trial setting for a CRO.
  • Previous experience managing full-service/global project management work in the CRO industry is essential.
  • Experience managing oncology studies.
  • 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, plus experience with CTMS, eTMF, EDC, and IXRS.
  • Ability to build positive working relationships with individuals and teams internally and externally.
  • Core understanding of medical terminology and clinical trial activities related to executing a clinical development plan.

Benefits

  • Supportive, collaborative work environment with a strong emphasis on work-life balance.
  • Opportunity to work on ground-breaking cancer therapies in a growing organization.
  • Exposure to a high-energy, dedicated team and dynamic project environment.
  • Equal Opportunity Employer status with accommodations available for candidates with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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