At a Glance
- Tasks: Manage clinical trials, coordinate with teams, and solve project challenges.
- Company: Dynamic healthcare company focused on innovative clinical solutions.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Exciting role with potential for career advancement in a supportive environment.
- Why this job: Join a team making a real difference in patient care and clinical research.
- Qualifications: 4+ years of clinical experience and strong communication skills required.
The predicted salary is between 46000 - 52000 £ per year.
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.
- 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 close-out visits, in addition to routine monitoring visits.
- Assure 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.
- Knowledge of FDA and/or EMA regulations (or relevant local regulations), ICH guidelines, and GCP governing the conduct of clinical studies.
- Working knowledge of Microsoft Word, PowerPoint, Project and Excel.
- At least 4+ years of clinical experience and a BS/BA in a relevant scientific discipline.
Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London employer: 3004 Syneos Health UK Limited
As a leading employer in the clinical research sector, we offer a dynamic and supportive work environment in London, where innovation and collaboration thrive. Our hybrid work model promotes flexibility, while our commitment to employee development ensures that you will have ample opportunities for growth and advancement in your career. Join us to be part of a team that values diversity, encourages professional development, and is dedicated to making a meaningful impact in the field of clinical trials.
Contact Details:
3004 Syneos Health UK Limited Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London
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We think you need these skills to ace Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London
Some tips for your application 🫡
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