Clinical Support Specialist Job at Syneos Health in Hyderabad. Candidates with TMF, QC, and clinical operations experience can apply online.
Company Overview
Syneos Health is a globally recognized life sciences organization delivering integrated clinical, medical, and commercial solutions. With operations across more than 100 countries, the company supports pharmaceutical and biotech firms throughout the drug development lifecycle. Syneos Health is known for its collaborative culture, innovation-driven approach, and commitment to improving patient outcomes worldwide.
Job Overview
| Job Title | Clinical Support Specialist |
|---|---|
| Company | Syneos Health |
| Location | Hyderabad (India) |
| Employment Type | Full-Time |
| Experience | 1–2 Years |
| Qualification | Associate Degree / Bachelor’s |
| Department | Clinical Operations |
| Job ID | 25106827 |
| Work Mode | Office-Based |
Job Location & Employment Type
- Location: Hyderabad (India)
- Work Type: Office-based
- Employment Type: Full-time
- Shift Flexibility: Must be comfortable working in EMEA time zone
Open Position / Department Details
This role is part of the Clinical Operations Support / Central Support Team, focusing on maintaining documentation, ensuring compliance, and supporting ongoing clinical trial activities. The position is ideal for candidates with experience in Trial Master File (TMF), quality control, and site contract processes.
Key Roles & Responsibilities
Clinical Trial Support
- Assist in study maintenance activities and support clinical operations teams
- Perform tasks assigned by the Central Support Team within defined scope
- Ensure alignment with study timelines and deliverables
TMF & Documentation Management
- Maintain and update Trial Master File (TMF) documentation
- Conduct TMF completeness checks and quality control (QC) reviews
- Ensure all documents are inspection-ready and compliant
Systems & Data Management
- Maintain clinical applications and internal systems
- Support data entry, tracking, and system updates
- Ensure accuracy and consistency of project data
Compliance & Quality Assurance
- Follow SOPs, Work Instructions, GCP, and ICH guidelines
- Ensure compliance with internal quality and performance standards
- Support audits and documentation reviews
Communication & Coordination
- Maintain effective communication with study teams and stakeholders
- Ensure timely completion of assigned tasks and deliverables
- Collaborate with cross-functional teams to meet project goals
Process Improvement
- Identify opportunities for process optimization and efficiency improvements
- Contribute to best practices within clinical operations
Eligibility Criteria
Education
- Associate degree or Bachelor’s degree in Life Sciences or related field
Experience
- Minimum 1–2 years of relevant experience in clinical operations
- Experience in TMF filing, QC, and site contracts is required
Skills Required
Technical Skills:
- Hands-on experience with Trial Master File (TMF) systems
- Knowledge of clinical trial processes and documentation standards
- Familiarity with electronic TMF systems and clinical tools
- Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
Core Skills:
- Strong communication skills (written and verbal English)
- Excellent organizational and time management abilities
- Ability to handle multiple tasks and meet deadlines
- Attention to detail and quality-focused approach
Additional Competencies:
- Ability to work independently and in a team environment
- Adaptability to fast-paced and dynamic work environments
- Willingness to learn and adopt new technologies
Salary & Benefits
- Salary: As per company norms
- Additional benefits may include training programs, career development, and performance incentives
Selection Process
The hiring process generally includes:
- Online application submission
- Resume screening
- Technical/functional interview
- HR round
- Final selection
How to Apply
Interested candidates can apply through the official Syneos Health careers portal using Job ID 25106827.
Important Dates
- Application Deadline: Not specified (apply early)
Why Apply for This Pharma Job?
- Opportunity to work in a global CRO environment
- Hands-on experience in TMF management and clinical documentation
- Exposure to international clinical trial processes
- Ideal role for professionals with 1–2 years experience in clinical operations
- Career growth opportunities in clinical research and regulatory domains
- Work with cross-functional teams in a dynamic and collaborative environment
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Syneos Health or any recruiter. We do not charge any fee for job postings or applications. Candidates are advised to verify details from the official website before applying.
Final Call-to-Action
If you have experience in TMF, clinical documentation, and quality control, this role offers a great opportunity to strengthen your career in clinical operations. Apply now and take the next step with Syneos Health.
