Clinical Trial Associate
- Contract Type
Our client is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases.
The Trial Associate provides administrative and operational support to the Global Medical Affairs department on assigned trial(s). Primary responsibilities focus on
tracking of metrics, report generation, monthly updates, processing and reconciliation of Trial Master File (TMF) documents, and generation of contract and purchase order requests.
Key responsibilities will include:
Liaise with the Legal department to facilitate, track, and expedite the contracting process for trial sites.
Maintain tracking systems for site and vendor contracts, site payments, and other tasks as identified.
Initiate payment requests for trial sites and vendors at direction of the Study Manager or designee Trial Support, Trial Master File (TMF), and Trial Documents.
Set up, maintenance, close out, and regular quality control of the TMFs, including
managing the reconciliation process.
Assist with the tracking, collation, review, distribution, and routing of trial documents.
Provide assistance with internal and external meetings
Facilitate the distribution and tracking of trial supplies
Support the development of agendas and meeting minutes for Study Team meetings.
Responsible for creating, disseminating, and evaluating metrics reports (i.e. enrollment, outstanding query and data reports, site startup status, etc.)
Accountable for contributing to the development of, understanding, and working to
compliance with relevant controlled documents (SOPs and work instructions)
Identify and escalate potential risks to Trial Specialist and/or Study Manager for
The ideal candidate will need the following experience / skills to be considered:
BA/BS or higher in life or health sciences preferred. Industry or relevant experience in lieu of education accepted.
Relevant experience in clinical science, clinical trial or site management, medical affairs, and/or drug development preferred.
Understanding basic GCP and GVP principals, their importance, and how they impact clinical trial activities.
Demonstrating knowledge of site and trial management practices, including site
evaluation, site staff training, patient recruitment, site initiation, sample management, and close out
We have a comprehensive benefits package and offer highly competitive remuneration.
If you have the required experience for this position and are eligible to work in the required location then please apply by CV or contact Natasha Campbell on 01628 587272.
To find out more about our company and search and apply for other open jobs please visit our website https://www.syneoshealth.com/
Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most. Evolve in a global company that is always looking for ways to work smarter and more efficiently as the only fully integrated Biopharmaceutical Accelerator. You'll be supported with comprehensive resources based on today's emerging technologies, data, science and knowledge - instead of practices from the past. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment to over-deliver and outperform. A career with Syneos Health means your everyday work improves patients’ lives around the world.