Syneos Health®, a global leader in biopharmaceutical solutions, is hiring for five critical roles across Technology, Clinical Development, Medical Writing, and Regulatory Publishing. These opportunities are available in Hyderabad (Hybrid/Office-based) and Remote (India), making them highly attractive for professionals in clinical research, regulatory affairs, medical writing, eCTD publishing, and technical project management.
Over the past five years, Syneos Health has supported 94% of FDA-approved novel drugs and 95% of EMA-authorized products, making it one of the most respected CROs globally. If you are looking to grow your career in a high-impact, global life sciences organization, these roles are worth applying for immediately.
Open Positions at Syneos Health (India)
1. Tech Project Manager I – Hyderabad (Hybrid)
Experience: 2–3 years
Key Skills: Project planning, stakeholder coordination, Agile/Waterfall, technology delivery
Responsibilities:
- Manage scope, schedule, and budget for assigned technology projects
- Coordinate with development, product, and client teams
- Track milestones, deliverables, and risks
- Support change management, training strategies, and resource planning
Qualification:
- Bachelor’s degree or equivalent project management experience
2. Senior Technical Business Analyst – Hyderabad
Experience: Mid to Senior level
Key Skills: Business analysis, Agile/Lean, stakeholder management, requirements gathering
Responsibilities:
- Capture and document business, functional, and non-functional requirements
- Translate business needs into use cases, epics, and user stories
- Act as liaison between technical teams and business stakeholders
- Mentor junior analysts and drive solution alignment
Qualification:
- Bachelor’s degree in Life Sciences, Communications, or related field
3. Sr. Medical Writer – ClinPharm (CSR, IB, Protocol) – Remote
Experience: 3–5 years
Key Skills: Clinical medical writing, ICH E3, FDA guidelines, AMA style
Responsibilities:
- Author CSRs, protocols, IBs, patient narratives, and regulatory documents
- Coordinate reviews with biostatistics, data management, and regulatory teams
- Ensure compliance with ICH, FDA, and company SOPs
- Mentor junior medical writers
Qualification:
- Strong experience in CRO, pharma, or biotech medical writing
4. Publisher II (CSR, IB, Protocol Publishing) – Remote
Experience: Relevant regulatory publishing experience
Key Skills: Document publishing, ICH/FDA/EU guidelines, quality checks
Responsibilities:
- Compile and publish regulatory and clinical documents
- Perform peer reviews and quality checks
- Collaborate with medical writers, editors, and cross-functional teams
- Train and mentor Publisher I staff
5. Senior Publishing Specialist (eCTD) – Remote
Experience: Moderate to senior level in regulatory publishing
Key Skills: eCTD, Extedo, ISI Toolbox, NDA/ANDA/IND submissions
Responsibilities:
- Build and publish eCTD submissions (Modules 1–5)
- Perform QC, validation, and troubleshooting
- Lead full regulatory submission builds
- Guide junior publishers and manage multiple projects
Why Work at Syneos Health?
- Global exposure across FDA, EMA, and international submissions
- Career development, technical training, and mentoring
- Strong work-life balance with remote and hybrid roles
- Inclusive “Total Self” culture
- Competitive compensation and rewards
Estimated Salary Range (India)
- Tech Project Manager I: ₹8 – 12 LPA
- Senior Technical Business Analyst: ₹12 – 18 LPA
- Sr. Medical Writer: ₹14 – 22 LPA
- Publisher II: ₹8 – 12 LPA
- Senior Publishing Specialist (eCTD): ₹15 – 25 LPA
(Salary may vary based on experience and interview performance)
How to Apply
Application Link For Tech Project Manager I – Hyderabad-Hybrid
Application Link For Senior Technical Business Analyst
Application Link For Sr. Medical Writer Clinpharm (CSR, IB, protocol)
Application Link For Publisher II (CSR , IB , Protocol publishing)
Application Link For Senior Publishing Specialist (eCTD )
