Career Opportunities: Join Syneos Health in Clinical Research
Job Summary
Syneos Health, a globally recognized Contract Research Organization (CRO) involved in the development of 94% of recent FDA-approved drugs, is currently seeking talented professionals to join its clinical operations and data programming teams. We are hiring for two high-impact roles: TMF Specialist I (Hybrid, Gurugram) and Clinical SAS Programmer II (Remote, India). These positions offer a unique opportunity to work on cutting-edge clinical trials, ensure global regulatory compliance, and advance your career within a high-performance, international environment.
1. TMF Specialist I (Gurugram – Hybrid)
Responsibilities
- Manage the full lifecycle of the Trial Master File (TMF), including initial set-up, ongoing maintenance, and final close-out.
- Ensure all documentation strictly adheres to ICH-GCP guidelines and relevant global regulatory standards.
- Perform document indexing, scanning, and uploading within eTMF systems.
- Conduct thorough Quality Reviews and completeness checks against Expected Document Lists.
- Maintain an “inspection-ready” status for all TMF documentation throughout the study lifecycle.
- Collaborate effectively with cross-functional study teams to ensure project success.
Requirements
- Education: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or BDS.
- Experience: A minimum of 6 months of experience as a Clinical Research Coordinator (CRC) or in a relevant clinical research environment is preferred.
- Knowledge: Strong understanding of TMF processes, clinical trial documentation, and regulatory compliance.
- Skills: Exceptional attention to detail, proficiency in Microsoft Office and Adobe Acrobat, and strong organizational and communication skills.
2. Clinical SAS Programmer II (Remote – India)
Responsibilities
- Develop and manage CDISC-compliant datasets to support clinical studies.
- Perform statistical programming using SAS, SQL, and R.
- Create advanced data visualizations using TIBCO Spotfire.
- Support the preparation of clinical trial reporting, including Tables, Listings, and Figures (TLFs).
- Lead or contribute to multiple studies while ensuring strict adherence to regulatory compliance.
- Partner closely with clinical data management and biostatistics teams to deliver high-quality data outputs.
Requirements
- Experience: 3+ years of professional experience in Clinical SAS Programming.
- Technical Expertise: Strong proficiency in Base/Advanced SAS, SQL, and R programming (including package development).
- Clinical Knowledge: Proven experience with clinical trial phases (I–IV) and data visualization tools like Spotfire.
- Preferred: Knowledge of Python and previous experience acting as a study lead is highly advantageous.
Benefits of Working at Syneos Health
- Global Impact: Participate in international clinical trials and gain exposure to FDA, EMA, and other global regulatory standards.
- Professional Growth: Access to structured career development, mentorship, and extensive training programs.
- Culture: Join a diverse and inclusive community of over 25,000 professionals working toward advancing patient health.
- Environment: A high-performance culture that values innovation and excellence in data and clinical operations.
How to Apply
We invite qualified candidates to submit their applications through the official company career portals provided below. Please select the link corresponding to the role for which you wish to apply:
Syneos Health is an equal opportunity employer committed to fostering an inclusive workplace.