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Clinical Project Manager

1 week, 5 days ago
Poland
Full-time
Senior
Project Manager
Project and Program Management
GCP
Apply Now
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012
View All Jobs 117

Description

  • Lead full-service clinical projects within budget and scope, including potential international trials.
  • Serve as the primary client liaison and support proposal activities and client presentations.
  • Coordinate with project teams and senior stakeholders across Precision and sponsor organizations, including executive leadership.
  • Oversee all aspects of clinical research trials across functional areas such as data management, safety, clinical operations, medical monitoring, and biostatistics.
  • Manage project delivery to agreed timelines, scope, cost, and quality standards.
  • Prepare project status updates, track key deliverables and performance metrics, and escalate issues as needed.
  • Support proposal strategy, study costing, and bid defense activities.
  • Review and prepare study documentation including protocols, project plans, informed consents, site contracts, and budgets.
  • Drive effective cross-functional study team coordination and execution.
  • Maintain client relationships and manage the project team and budget through study completion.

Requirements

  • Degree or equivalent combination of education and experience in a life science-related field.
  • 5 to 7 years of industry experience, including at least 4 years of full-service project management experience in a clinical trial setting at 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.
  • Experience with CTMS, eTMF, EDC, and IXRS systems.
  • Ability to build positive working relationships with internal and external stakeholders.
  • Understanding of medical terminology and clinical trial activities within a clinical development plan.

Benefits

  • Annual discretionary bonus.
  • Private medical insurance.
  • MultiSport Card.
  • Life insurance.
  • Pension plan.
  • Home working allowance.
  • Vacation leave.
  • Competitive compensation range in Poland: 350,200 to 525,200 PLN gross per annum.

Interested in this position?

Apply directly on the company website

Apply Now

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