Clinical Project Manager

4 weeks ago
Full-time
Senior
Project and Program Management
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

Description

  • Lead full-service clinical projects in line with the study budget, scope of work, timelines, and quality expectations.
  • Serve as the primary client liaison and participate in proposal activities and client presentations.
  • Manage all stages of the study lifecycle, including proposal strategy, development, costing, bid defense, and study closeout.
  • Coordinate and oversee cross-functional project teams across internal departments and external stakeholders.
  • Provide total project management oversight for functional areas including data management, safety, clinical, medical monitoring, and biostatistics.
  • Prepare project status updates, performance metrics, deliverable tracking, and escalation reports for clients and management.
  • Review and prepare study documentation, including protocols, project plans, informed consents, site contracts, and budgets.
  • Liaise with sponsors and senior leadership, including C-level stakeholders, to support trial delivery and issue resolution.
  • Drive efficient trial execution and maintain accountability for project delivery across global or regional studies.

Requirements

  • Degree or similar life science qualification, or an equivalent 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 within a CRO.
  • Previous experience managing full-service/global project management responsibilities in the CRO industry is essential.
  • Experience managing oncology studies.
  • Working understanding 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.
  • Proven computer skills with MS Office, MS Project, and PowerPoint, plus experience with CTMS, eTMF, EDC, and IXRS software.
  • Ability to develop positive working relationships with individuals and teams internally and externally.
  • Demonstrated understanding of medical terminology and clinical trial activities related to clinical development plans.

Benefits

  • Supportive, collaborative, people-focused CRO environment.
  • Work-life balance encouraged.
  • Opportunities for team development and growth.
  • High-energy, dynamic team culture.
  • Equal Opportunity Employer status.
  • Reasonable accommodation available for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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