Description
Syneos Health is seeking a Single Sponsor Clinical Project Manager II (Virology) to join their team.
The successful candidate will be responsible for managing clinical projects, specifically in the virology team, with 1-2 days in Uxbridge and office move to Central London in May 2026.
Job Responsibilities:
- Plan, direct, create, and communicate clinical study timelines to ensure deliverables are produced on schedule
- Gather input from cross-functional teams to create comprehensive plans for clinical studies
- Ensure consistency of clinical study processes across clinical trials, adhering to standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations
- Oversee and resolve operational aspects of clinical trials in conjunction with project teams
- Select sites and vendors, prepare clinical trial budgets, and ensure studies are conducted within clinical trial protocols
- Monitor progress and follow up with team members and line managers when issues develop
- Implement and prepare the clinical development strategy as outlined by the clinical teams
- Develop trial recruitment strategies to ensure successful participant enrollment
Qualifications:
- Bachelor's degree in a related field (e.g., Clinical Research, Life Sciences, Healthcare Management)
- Minimum of 5 years of experience in clinical project management or a related role
- Proven track record of successfully managing clinical trials and ensuring adherence to SOP, GCP, and country regulations
Certifications:
- Certification in Clinical Research (e.g., CCRP, CCRA) is preferred
- Project Management Professional (PMP) certification is a plus
Necessary Skills:
- Strong organizational and planning skills to create and manage clinical study timelines
- Excellent communication skills to gather input from cross-functional teams and communicate plans effectively
- Ability to oversee and resolve operational aspects of clinical trials
- Knowledge of SOP, GCP, and country regulations to ensure consistency across clinical studies
- Experience in site and vendor selection, budget preparation, and monitoring progress
- Ability to implement and prepare clinical development strategies
- Strong problem-solving skills to address issues that arise during clinical trials