At a Glance
- Tasks: Coordinate clinical research activities and ensure compliance with study protocols.
- Company: Join a leading clinical research organisation with a commitment to innovation.
- Benefits: Flexible working hours, competitive pay, and opportunities for professional growth.
- Other info: Enjoy a collaborative team atmosphere with potential for career advancement.
- Why this job: Be part of impactful clinical studies and enhance your skills in a dynamic environment.
- Qualifications: High school diploma, strong communication skills, and a willingness to learn new technologies.
The predicted salary is between 30000 - 40000 £ per year.
Job Responsibilities
- Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions.
- Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines.
- Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits.
- Prepares and maintains site manuals, reference tools and other documents.
- Maintains, updates, and inputs clinical tracking information into databases.
- Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client.
- Manages shared mailbox, processes site requests and routes correspondence appropriately.
- Coordinates the ordering, packaging, shipping and tracking of site supplies and materials.
- Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items.
- May handle receipt, tracking and disposition of Case Report Forms and Queries.
- Maintains overall awareness in the field of clinical research by completing all necessary and assigned training.
Qualifications
- High School diploma or equivalent.
- Good communication and interpersonal skills.
- Ability to embrace new technologies.
- Minimal travel up to 25% may be required.
Equal Opportunity Statement
Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against.
If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at: Email: jobs@syneoshealth.com. One of our staff members will work with you to provide alternate means to submit your application.
FSP Country Coordinator - 2-3 days a week at client office (Uxbridge) employer: Syneos Health, Inc.
Syneos Health® is an exceptional employer, offering a dynamic work environment in the heart of London where innovation meets collaboration. With a strong commitment to employee growth, we provide extensive training and development opportunities, ensuring our team members thrive in their careers while contributing to meaningful projects in oncology. Our inclusive culture fosters teamwork and creativity, making us a leading choice for professionals seeking to make a significant impact in the life sciences sector.
