Clinical Job Alert at Syneos Health | Apply Now
Looking for a clinical job in the life sciences industry? Syneos Health is hiring a Clinical Study Administrator under Country Operations Management. This is an exciting opportunity for candidates seeking syneos health careers and a rewarding life science job in clinical research, offering hands-on experience in global trials and collaboration with industry experts.
Job Details
- Job Position: Clinical Study Administrator (CSA)
- Job Location: Boston, MA (Seaport area)
About the Company
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. The company partners with innovators across the drug development and commercialization continuum, helping them navigate complexity, anticipate change, and accelerate progress.
With a strong presence in Syneos Health careers, the organization focuses on delivering impactful solutions through collaboration, innovation, and expertise. Over the past five years, Syneos Health has contributed to 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products.
Job Description
This clinical job involves working as a Clinical Study Administrator within the Country Operations Management team. The role supports rare disease trials and offers a unique combination of sponsor collaboration and CRO resources.
As part of this life science job, you will collaborate with Project Managers, Clinical Research Associates, Study Start-Up Managers, and other stakeholders to ensure the smooth execution of clinical trials across regions.
Qualifications
- Bachelor’s Degree in a related discipline (preferably life sciences)
- Proficiency in MS Office Suite (Excel, Word, PowerPoint)
- Understanding of the drug development process
- 1+ years of experience in pharmaceutical or clinical research industry
- Strong organizational and multitasking skills
- Excellent attention to detail
- Effective written and verbal communication skills
- Strong collaboration and interpersonal abilities
Key Responsibilities
- Provide support to the local study team in achieving quality and timely study deliverables across the clinical trial lifecycle
- Manage end-to-end electronic Trial Master File (eTMF) set-up and maintenance
- Track regulatory documents, training documentation, and milestones in CTMS
- Support start-up activities including CDA negotiation, document collection, and site communication
- Assist in site preparation, activation, and documentation processes
- Collaborate with study teams and vendors for clinical trial supply management
- Act as a central communication point for project-related documentation
- Contribute to global tracking tools such as CTMS and Smartsheets
- Assist with regulatory submissions and local language translations
- Support team meetings, teleconferences, and onboarding activities
Life Science Job Benefits
- Strong career development and progression opportunities
- Inclusive and supportive work culture
- Competitive total rewards and recognition programs
- Exposure to global clinical trials and cutting-edge research
- Flexible work environment with work-life balance benefits
