Single Sponsor Clinical Project Manager II UK (Oncology) UK based (Days at client site, London)

We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Job Responsibilities

• Project leadership and delivery: manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP’s, and regulatory requirements.
• Acts as primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the contractual agreement.
• Leads project team to ensure quality, timelines, and budget management.
• Accountable for the financial performance of each project and coordinates activities and deliverables of all study conduct partners.
• Ensures studies are conducted in compliance with GCP, relevant SOP’s and regulatory requirements.
• Responsible for quality and completeness of TMF for assigned projects.
• Maintains study information on a variety of databases and systems.
• Manages study inspection readiness and implements project plans.
• Plans, coordinates and presents at internal and external meetings and prepares project management reports for clients and management.
• Develops contingency planning and risk mitigation strategies.
• Builds strong relationships with current clients to generate new and/or add‑on business.
• Participates in bid defense meetings where presented as potential project manager.
• May line‑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.
• Clinical research organization (CRO) and relevant therapeutic experience preferred.
• Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
• Strong organizational and time‑management skills.
• Direct therapeutic area expertise.
• Ability to embrace new technologies.
• Excellent communication, presentation, interpersonal skills, both written and spoken.
• Ability to travel approximately 25% of the time.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks at its discretion. Equivalent experience, skills, and education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate.