Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge
Updated: May 28, 2026
Location: GBR-London-Hybrid
Job ID: 25109273
Description
Single Sponsor Clinical Project Manager II (Virology) – responsible for planning, directing, creating, and communicating clinical study timelines in a 3‑day per week schedule in Uxbridge.
Syneos Health is a leading integrated biopharmaceutical solutions organization focused on accelerating customer success in drug development and commercialization.
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 trials, adhering to SOP, GCP, and country regulations.
* Oversee and resolve operational aspects of clinical trials in conjunction with project teams.
* Select sites and vendors, prepare trial budgets, and ensure studies are conducted within 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 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.
Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability, or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at jobs@syneoshealth.com.
Phone: 919 876 9300
Fax: 919 876 9360
Toll-Free: 866 462 7373
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