At a Glance
- Tasks: Manage clinical trials, coordinate with teams, and ensure project goals are met.
- Company: Join a leading health organisation focused on innovative clinical solutions.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Work with a diverse team and gain exposure to cutting-edge clinical research.
- Why this job: Make a difference in healthcare while developing your skills in a dynamic environment.
- Qualifications: 4+ years of clinical experience and strong communication skills required.
The predicted salary is between 55000 - 65000 £ per year.
Location: London, POST-LON, United Kingdom
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 and 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.
- Update study timelines.
- Participate in departmental, or interdepartmental, strategic initiatives under general supervision.
- Review routine data and prepare safety, interim, and final study reports and resolve data discrepancies.
- Conduct site evaluation, initiation, co-monitoring, and closeout 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 and experience with Word, PowerPoint, Project and Excel.
- At least 4+ years of clinical experience and a BS/BA in a relevant scientific discipline.
EEO Statement: Syneos Health is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London employer: Syneos Health, Inc.
At Syneos Health, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of London. Our commitment to employee growth is evident through comprehensive training programmes and opportunities to engage in strategic initiatives, ensuring that every team member can thrive in their career while contributing to meaningful clinical research. With a hybrid working model, we provide the flexibility needed to balance professional and personal commitments, making us an attractive choice for those seeking rewarding employment in the clinical trial management field.
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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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Syneos Health, Inc. that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
