Syneos Health Clinical Support Specialist TMF
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Clinical Operations Support
- Compliance & Quality Management
- Collaboration & Communication
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What experience is required for this role?
- 2. What qualifications are required?
- 3. What are the main responsibilities?
- 4. Is this role suitable for freshers?
- 5. What is the career growth?
- Summary Table
Syneos Health Hiring Clinical Support Specialist (Site Contracts) | Hyderabad Clinical Trials Jobs
Syneos Health is hiring Clinical Support Specialist (Site Contracts) professionals for its Hyderabad clinical operations team. This is a full-time, on-site opportunity designed for candidates with 1–2 years of experience in clinical research, Trial Master File (TMF) management, and site contract support. The role focuses on clinical trial documentation, regulatory compliance, and global study coordination, making it a strong career opportunity in clinical operations and CRO environments.
Company Overview
Syneos Health is a leading global biopharmaceutical solutions organization that integrates clinical development, medical affairs, and commercial services. With operations in over 110 countries and a workforce of more than 29,000 professionals, the company supports pharmaceutical and biotech organizations in accelerating drug development and market access.
The organization has contributed to over 90% of FDA-approved drugs and a significant number of EMA-authorized products. Known for its patient-centric approach and innovation-driven clinical development model, Syneos Health provides professionals with exposure to global trials, advanced systems, and regulatory frameworks.
Job Role & Responsibilities
As a Clinical Support Specialist (Site Contracts), you will play a key role in supporting clinical trial operations, maintaining TMF documentation, and ensuring compliance with global regulatory standards.
Core Responsibilities
- Maintain and manage Trial Master File (TMF) documentation and ensure completeness
- Perform TMF quality control (QC) checks and document reviews
- Support site contract activities and clinical trial documentation workflows
- Ensure all documents comply with SOPs, GCP, and ICH guidelines
Clinical Operations Support
- Assist in study maintenance activities and project support tasks
- Maintain clinical systems and internal applications used for trial management
- Support Central Support Team activities for global clinical trials
- Ensure timely completion of assigned deliverables
Compliance & Quality Management
- Ensure adherence to corporate policies, SOPs, and regulatory requirements
- Maintain audit-ready documentation and support inspection readiness
- Identify process improvements and contribute to operational efficiency
Collaboration & Communication
- Communicate effectively with cross-functional teams and study stakeholders
- Support project teams in meeting timelines and deliverables
- Manage multiple tasks in a dynamic clinical research environment
Eligibility / Qualifications
Educational Qualification
Candidates must have relevant educational background in healthcare or life sciences.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Clinical Research, Biomedical Sciences
Experience
- Minimum 1–2 years of experience in clinical research or CRO environment
- Hands-on experience in TMF filing, QC, and site contract management required
Skills Required
- Strong knowledge of clinical trials and regulatory guidelines (ICH-GCP)
- Experience with electronic TMF systems and clinical applications
- Proficiency in Microsoft Office (Excel, Word, Outlook, PowerPoint)
- Excellent communication and interpersonal skills
- Strong attention to detail and organizational abilities
- Ability to work in EMEA time zone and handle multiple priorities
Location & Salary
- Job Location: Hyderabad, India (On-site)
- Employment Type: Full-time
- Salary: Competitive salary aligned with CRO and clinical operations roles
Application Process
Interested candidates can apply through the official Syneos Health careers portal:
Frequently Asked Questions (FAQs)
1. What experience is required for this role?
Candidates need 1–2 years of experience in clinical research, especially in TMF and site contracts.
2. What qualifications are required?
A degree in Life Sciences, Pharmacy, or Clinical Research is required.
3. What are the main responsibilities?
TMF management, quality checks, clinical documentation, and site contract support.
4. Is this role suitable for freshers?
No. Candidates with prior experience are preferred.
5. What is the career growth?
You can grow into Clinical Trial Associate, Clinical Operations Specialist, or Project Management roles.
Summary Table
| Category | Details |
|---|---|
| Company | Syneos Health |
| Vacancies | Clinical Support Specialist (Site Contracts) |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Clinical Research |
| Experience | 1–2 Years Clinical Research / TMF Experience |
To apply for this job please visit syneoshealth.wd12.myworkdayjobs.com.
