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.
Coordinates CROs and vendors.
Responsible in updating of study timelines.

At least 4+ years of clinical experience and a BS/BA in a relevant scientific discipline.
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.

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.
25 days annual leave
Private healthcare
Pension scheme
Flexible working hours

Single Sponsor Clinical Trial Manager I, French speaking

Key skills