Syneos Health, a global biopharmaceutical leader, is expanding its India operations with exciting openings for Senior Publishing Specialist (eCTD), Clinical Trial Manager, and Site Contract Specialist.
With over 29,000 employees across 110 countries, Syneos Health delivers end-to-end clinical, regulatory, and commercial solutions that power global healthcare innovation. This is your opportunity to join a team that has supported 94% of all FDA-approved drugs in the last five years.
🧩 Available Positions
1. Senior Publishing Specialist (eCTD) – Remote (India)
Job ID: 25102356 | Type: Full-Time | Location: Remote
Key Responsibilities:
- Perform eCTD publishing tasks: compilation, QC, hyperlinking, bookmarking, and submission validation.
- Prepare regulatory submissions (INDs, NDAs, ANDAs, DMFs, variations).
- Troubleshoot issues with eCTD builds and assist junior publishers.
- Use tools such as Extedo’s eCTDManager, CoreDossier, ISI Toolbox, and Acrobat.
Qualifications:
- Experience in regulatory publishing within pharma or biologics.
- Knowledge of ICH guidelines, EMA/FDA submission standards.
- Proficiency in MS Office and eCTD publishing software.
- Strong attention to detail and ability to multitask.
2. Clinical Trial Manager – Hyderabad (Hybrid)
Job ID: 25103286 | Type: Full-Time | Location: Hyderabad (Hybrid)
Responsibilities:
- Manage end-to-end clinical study execution ensuring compliance and data quality.
- Lead study teams, coordinate with global stakeholders, and oversee site operations.
- Drive inspection readiness and adherence to regulatory timelines.
Qualifications:
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, or related field.
- 4–8 years of clinical project management experience.
- Excellent leadership and cross-functional communication skills.
3. Site Contract Specialist – Hyderabad (Hybrid)
Job ID: 25103283 | Type: Full-Time | Location: Hyderabad
Responsibilities:
- Draft, review, and negotiate site contracts for clinical studies.
- Ensure compliance with local laws, company policies, and timelines.
- Collaborate with internal legal and clinical teams for smooth contract execution.
Qualifications:
- Degree in Law, Pharmacy, or Life Sciences.
- 2–5 years of experience in site contracting within CRO/pharma industry.
- Detail-oriented with strong stakeholder management skills.
🌟 Why Join Syneos Health?
- Competitive salary and performance incentives.
- Global exposure in regulatory and clinical operations.
- Supportive leadership, career development programs, and technical training.
- Inclusive “Total Self” culture valuing authenticity and collaboration.
📝 How to Apply
Application Link for Senior Publishing Specialist (eCTD) – Remote (India)
Application Link for Clinical Trial Manager – Hyderabad (Hybrid)
Application Link for Site Contract Specialist – Hyderabad (Hybrid)
