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Senior Project Manager - Clinical Trials

2 hours, 15 minutes ago
Serbia
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 47

Description

  • Lead full-service clinical projects within agreed budget, scope, timelines, and quality standards.
  • Serve as the primary client contact and provide customer service throughout the study lifecycle.
  • Participate in proposal strategy, development, costing, bid defense, and client presentations.
  • Manage clinical trials from study start-up through completion across phases I-IV.
  • Oversee all functional departments, including data management, safety, clinical, medical monitoring, and biostatistics.
  • Coordinate cross-functional internal and external stakeholders, including sponsors and senior leadership.
  • Prepare project status updates, performance metrics, deliverables tracking, and escalation plans.
  • Review and prepare protocols, project plans, informed consents, site contracts, and budgets.
  • Support efficient study execution by actively contributing as a member of the project team.
  • Lead international trials when required.

Requirements

  • Degree or equivalent life science qualification, or an equivalent combination of education and experience.
  • 5 to 7 years of industry experience.
  • At least 4 years of full-service Project Management experience in a clinical trial setting within a CRO.
  • Previous experience in a full-service/global Project Management role in the CRO industry is essential.
  • Experience managing studies in Oncology is required; Rare Diseases or CNS experience is also relevant.
  • Working understanding of GCP/ICH guidelines and the clinical development process.
  • Ability and willingness to travel domestically and internationally, including overnight stays.
  • Strong written and spoken English communication skills.
  • Strong presentation skills.
  • Proficiency with MS Office, MS Project, PowerPoint, and clinical systems such as CTMS, eTMF, EDC, and IXRS.

Benefits

  • Supportive, collaborative, and people-focused CRO environment.
  • Emphasis on work-life balance.
  • Opportunities for team development and growth.
  • Chance to work on groundbreaking cancer therapy research and precision medicine programs.
  • Equal Opportunity Employer commitment.
  • Reasonable accommodation available for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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