Global Oncology Study Lead | Senior PM (Remote)

Syneos Health, Inc.

Greater London

Hybrid

GBP 90,000 - 130,000

Full time

14 days+
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Job summary

Syneos Health is seeking a Global Study Manager (Oncology) / Sr PM for sponsor-dedicated projects across EMEA, working remotely from the UK. You will lead interdisciplinary clinical research programs, ensuring GCP compliance, timelines, and budget control while maintaining strong client communications.

The role requires strong knowledge of GCP/ICH guidelines, regulatory requirements, and drug development processes, with CRO experience preferred.

Qualifications

  • GCP/ICH guidelines, regulatory requirements and drug development process familiarity.
  • Clinical monitoring procedures experience is preferred.
  • CRO experience and therapeutic exposure are advantageous.

Responsibilities

  • Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with GCPs, SOPs and regulatory requirements.
  • Acts as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout according to contractual agreements.
  • Leads clinical team to ensure quality, timelines and budget management.
  • Accountable for the financial performance of assigned projects
  • Accountable for all project deliverables for assigned projects and/or project regions.
  • Coordinates activities and deliverables of all project conduct partners and proactively identifies and manages issues.
  • Maintains project information on databases, tracks progress, and prepares management reports.
  • Provides oversight for project plans, risk mitigation, and contingency planning.

Skills

GCP/ICH guidelines
Regulatory requirements
Drug development process
Clinical monitoring procedures

Education

Bachelor’s Degree in life sciences/Medicine/Pharmacy/Nursing or related field
Equivalent combination of education and experience

Job description

Syneos Health is seeking a Global Study Manager (Oncology) / Sr PM for sponsor-dedicated projects across EMEA, working remotely from the UK. You will lead interdisciplinary clinical research programs, ensuring GCP compliance, timelines, and budget control while maintaining strong client communications.

The role requires strong knowledge of GCP/ICH guidelines, regulatory requirements, and drug development processes, with CRO experience preferred.

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