Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. 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.

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.

Job Responsibilities:

• Prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions.
• Participate in and manage project meetings and conference calls with CROs, vendors, and multi-functional teams.
• Able to anticipate obstacles and proactively develop solutions to achieve project goals.
• Develop a general understanding of functional issues and routine project goals from an organizational perspective.
• Participate in abstract presentations, oral presentations, and manuscript development activities.
• Interact and cooperate with individuals in other functional areas to address routine study issues.
• Develop tools and processes that increase measured efficiencies of the project.
• Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).
• Assist in selecting Contract Research Organizations (CROs) or vendors.
• Coordinate CROs and vendors.
• Responsible for updating study timelines.
• Participate in departmental, or interdepartmental, strategic initiatives under general supervision.
• Assist in review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies.
• Conduct site evaluation, initiation, co-monitoring, and closeout visits, in addition to the routine monitoring visits.
• Assure the site compliance with the protocol and regulatory requirements for assigned studies.
• Draft and coordinate review of protocols, informed consents, case report forms, and study plans as needed.

Skills and experience:

• Excellent verbal, written, interpersonal and presentation skills are required.
• Knowledge of FDA and/or EMA Regulations (or relevant local regulations), ICH Guidelines, and GCP governing the conduct of clinical studies.
• Working knowledge and experience with Word, PowerPoint, Project and Excel.
• At least 4+ years of clinical experience and a BS/BA in a relevant scientific discipline.

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, and 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.