Syneos Health
Single Sponsor Clinical Project Manager II UK (Oncology)
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Single Sponsor Clinical Project Manager II UK (Oncology)
Single Sponsor Clinical Project Manager II (Oncology) – UK
(Syneos Health®)
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators across the drug development and commercialization continuum, helping them navigate complexity, anticipate change, and accelerate progress.
About the Role
Our Clinical Solutions team members operate with a drug development mindset, applying decades of experience and deep expertise to fully grasp customer needs and translate them into tailored solutions. Whether as a Functional Service Provider or in a Full-Service capacity, you’ll collaborate with passionate problem solvers, driving solutions as a team to help our customers achieve their goals. We thrive on agility and delivering results—for one another, our customers, and most importantly, those in need.
Why work at Syneos Health?
- Empowering career growth: Through career development, progression, technical training, peer recognition, and competitive rewards.
- Inclusive culture: A place where you can be authentically yourself—centered on our purpose, Driven to Deliver, shaping solutions that transform lives.
- Global collaboration: By bringing together dynamic colleagues worldwide, we define the future of healthcare and accelerate patient progress.
Move discovered more with #SyneosHealthRetweet https://syneoshealth.com
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Job Responsibilities
Project Leadership & Delivery
- Manage interdisciplinary clinical research studies, ensuring compliance with Good Clinical Practice (GCP), relevant SOPs, and regulatory requirements.
- Act as the primary liaison between Syneos Health and the customer, guaranteeing timely study launch, conduct, and closeout per contractual agreements.
- Lead project teams to deliver on quality, timelines, and budget management; accountable for financial performance per project.
- Coordinate study conduct partners and proactively manage issues.
- Ensure adherence to GCP, SOPs, and regulatory requirements for all studies.
- Oversee TMF quality and completeness and maintain study databases/plugins.
- Lead inspection readiness preparations, covering all study aspects.
- Develop and implement project plans, coordinate internal/external meetings, and present reports.
- Create contingency plans and risk mitigation strategies to ensure successful study delivery.
- Build customer relationships to drive new/additional business opportunities.
- May participate in bid defense as the designated project manager for proposals and manage clinical staff/project teams as required.
Key Competencies
- Experience in oncology (preferred).
- Deep expertise in clinical operations, regulatory compliance, and study management.
- Ability to handle high workloads independently with precision and deadlines.
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Requirements
Qualifications & Experience
- Education: Bachelor’s degree in life sciences, Medicine, Pharmacy, Nursing, or equivalent education + experience.
- Experience:
- Clinical Research Organization (CRO) experience (preferred).
- Domain Oncology is highly desirable (önetics needed to be strongly articulated in future roles).
- Regulatory/Electivity expertise: Strong knowledge of GCP/ICH guidelines and compliant documentation.
- Proficiency: Advanced Excel (including VLOOKUP/XLOOKUP) highly advantageous.
Skills
- Organizational skills: Ability to manage multiple studies and deadlines with minimal supervision.
- Communications: Fluent in English (written/spoken), with professional presentation skills.
- Travel: Demonstrated willingness to serve up to ~25% (potentially ad-hoc).
Why Join Us?
Our passion for the challenges in healthcare is matched by a commitment to progress.
Discover more: Official Link | International reach with 29,000+ employees supporting patient needs globally.
Common Application Note
Note: Primary details and duties may evolve; key tasks, duties, and inflexible responsibilities will be clearly documented in a formal job description / Company personnel. This remains a dynamic space subject to Company discretion.
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