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Senior Project Manager - Clinical Trials

3 hours, 59 minutes ago
Slovakia
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 4

Description

  • Independently lead full-service clinical projects in line with study budget and scope of work.
  • Serve as the primary client liaison and participate in proposal activities and client presentations.
  • Oversee clinical project delivery across global and regional phase I-IV trials in oncology, rare diseases, or CNS.
  • Manage all functional areas of the trial, including data management, safety, clinical, medical monitoring, and biostatistics.
  • Coordinate cross-functional internal and external stakeholders to support efficient trial execution.
  • Monitor project timelines, scope, cost, and quality, and escalate issues as needed.
  • Prepare project status updates for clients and senior management, including deliverables and performance metrics.
  • Review and prepare study documents such as protocols, project plans, informed consents, site contracts, and budgets.
  • Support proposal strategy, costing, and bid defence activities.
  • Maintain and manage client relationships, project teams, and budgets throughout the study lifecycle.

Requirements

  • Degree or similar life science qualification, 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.
  • Previous experience in a full-service/global Project Management role within the CRO industry is essential.
  • Experience managing oncology studies is required or strongly preferred.
  • Working knowledge of GCP/ICH guidelines and the clinical development process.
  • Ability to travel domestically and internationally, including overnight stays.
  • Strong English communication skills, both written and spoken.
  • Strong presentation skills.
  • Proven computer skills 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 clinical development planning.

Benefits

  • Join a supportive, collaborative, people-focused CRO environment.
  • Work in a high-energy team that values challenge, detail, and dynamic work.
  • Opportunity to support global oncology and rare disease research.
  • Work-life balance is actively encouraged.
  • Team development and employee appreciation are emphasized.

Interested in this position?

Apply directly on the company website

Apply Now

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