About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. 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.
Job Responsibilities
* Therapeutic Area: CAR T cell therapy, cutting-edge science, and oncology - Multiple Myeloma.
* Coordinate Phase III clinical research studies across European, ensuring all aspects of the study are meticulously planned and executed.
* 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.
* Participate in abstract presentations, oral presentations and manuscript development activities.
* Interact and cooperate with individuals in other functional areas to address routine study issues.
* Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).
* Assist in selecting CRO's or Vendors.
* Coordinates CROs and Vendors.
* Responsible in updating of study timelines.
* Ensure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updates.
Qualifications
* Bachelor's degree in a related field (e.g., life sciences, clinical research).
* Regional Study Management experience in managing studies across European regions.
* In-depth knowledge of clinical research processes and regulations gained from a CRO or Pharma.
* CRO oversight experience.
* Strong project management and organizational skills.
* Excellent communication and interpersonal skills.
* Ability to work independently and as part of a team.
* Proficiency in using clinical trial management software and tools.
Note
Our client will be moving to Central London Q2 - 2027.
Necessary Skills
* Strong analytical and problem-solving skills.
* Attention to detail and accuracy.
* Ability to manage multiple projects and priorities simultaneously.
* Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
* Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
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