Single Sponsor - Clinical Project Manager II (Late phase) UK based. in London

Syneos Health is a leading integrated life sciences services organization that supports clients throughout drug development and commercialization. Clinical Solutions team members bring a drug‑development mindset, extensive experience, and deep expertise to understand customer needs and shape solutions that accelerate progress.

Job Responsibilities

• Project Leadership and Delivery – manage a clinical research study as a project manager, ensuring compliance with GCP, SOPs, and regulatory requirements.
• Act as primary liaison between Company and Customer to ensure timely study launch, conduct, and close‑out according to contractual agreements.
• Lead project team to ensure quality, timelines, and budget management.
• Accountable for financial performance of each project; coordinate activities and deliverables of study conduct partners and proactively manage issues.
• Ensure studies are conducted in compliance with GCP, relevant SOPs and regulatory requirements; accountable for all project deliverables.
• Responsible for quality and completeness of TMF for assigned projects.
• Maintain study information in various databases and systems.
• Responsible for study management components of inspection readiness for all aspects of conduct; oversee development and implementation of project plans.
• Plan, coordinate and present at internal and external meetings; prepare project management reports for clients and management.
• Develop contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
• Build strong relationships with current clients to generate new or add‑on business for the future.
• May participate in bid defense meetings where presented as potential project manager.
• May manage other project‑management team members and clinical monitoring staff.

Qualifications

• Bachelor’s Degree (or equivalent) in life sciences, medicine, pharmacy, nursing, or equivalent combination of education and experience.
• Experience with a clinical research organization (CRO) and relevant therapeutic area preferred; strong knowledge of GCP/ICH guidelines and related regulatory requirements.
• Experience with real‑world evidence in a CRO or pharmaceutical environment.
• Strong organizational and time‑management skills; able to work independently.
• Direct therapeutic area expertise.
• Ability to embrace new technologies.
• Excellent communication, presentation, and interpersonal skills, both written and spoken.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, or job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Nothing contained herein should be construed to create an employment contract. The Company’s employment is governed by applicable laws including the EU Equality Directive. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate. Syneos Health is an equal opportunity employer and a diverse workforce is crucial to our success.