Clinical Study Job at Syneos Health, USA | Life Sciences | Apply Now
Joining Syneos Health in Morrisville, NC, as a Clinical Study Administrator (CSA) offers a unique opportunity to sit at the intersection of a global Contract Research Organization (CRO) and a dedicated sponsor team. In this Clinical Study Job, you won’t just be managing paperwork; you’ll be a vital engine driving rare disease trials forward. By choosing a Syneos Health Career, you join a culture that is “Driven to Deliver,” working with a team that has contributed to 94% of all novel FDA-approved drugs over the last five years.
- Job Position: Clinical Study Administrator, Country Operations Management
- Location: Morrisville, NC
About The Company
Syneos Health is a leading fully-integrated life sciences services organization. They partner with innovators to navigate the complexities of the drug development continuum. Their team members apply a “drug development mindset,” ensuring that every solution is shaped by deep therapeutic expertise. With 25,000 colleagues worldwide, the scale of your impact is massive, helping to define the pace of patient progress across 73,000 sites globally. Syneos Health Careers are built on a foundation of belonging, where colleagues are encouraged to be their authentic selves while shaping the future of healthcare.
Your Impact in this Clinical Study Job – Key Responsibilities
As a CSA in Country Operations Management (COM), you are the central point of contact for the local study team. Your role is pivotal in ensuring the quality and timeliness of deliverables across the entire study lifecycle.
Strategic Support and Startup Excellence
- Deliverable Management: Support the COM team in site identification, feasibility, and recruitment to ensure trials stay on track.
- Startup Phase: Handle CDA delivery and negotiation, distribute and collect essential documents, and prepare sites for activation.
- Collaboration: Work alongside Study Start-Up Managers and CRAs to handle the distribution of clinical trial supplies and maintain tracking information.
Data Integrity and Documentation
- eTMF Management: Take responsibility for the end-to-end electronic Trial Master File (eTMF) setup and maintenance, ensuring all regulatory documents are tracked accurately.
- CTMS Oversight: Manage milestones within the Clinical Trial Management System (CTMS) and utilize tools like Smartsheet to maintain global tracking.
- Compliance: Assist with local language translations and IRB/CEC/CA submissions in collaboration with Regulatory Affairs.
Qualifications for this Life Science Job
To excel in this role, Syneos Health is looking for motivated professionals who understand the high stakes of rare disease research.
- Education: Bachelor’s Degree in a related discipline, preferably Life Science.
- Experience: 1+ years of experience in the pharmaceutical industry specifically focused on the delivery of clinical studies.
- Technical Proficiency: Strong command of the MS Office Suite (Excel, Word, PowerPoint) and a solid understanding of the drug development process.
- Core Competencies:
- Meticulous attention to detail.
- Excellent collaboration and interpersonal skills.
- Strong organizational skills with the ability to manage competing priorities.
In summary, this Clinical Study Job at Syneos Health provides a “best of both worlds” scenario: the dedicated focus of a sponsor-dedicated role with the vast resources and stability of a global CRO. By advancing your Syneos Health Career in 2026, you become a “passionate problem solver” dedicated to those in need. If you have the organizational rigor to manage eTMF documentation and the interpersonal skills to lead site communications, this Life Science Job in Morrisville offers the perfect platform to dramatically impact patient progress in the rare disease space.
