Syneos Health has announced multiple exciting openings for life sciences professionals in India. The company is currently hiring for Medical Writer II (MLR Reviewer + Veeva), Medical Writer I (Junior Project Specialist), and Clinical Data Reviewer (Centralized Monitoring/Clinical Scientist Support) roles.

These opportunities are ideal for candidates with backgrounds in PharmD, M.Pharm, B.Pharm, MBBS, Life Sciences, Clinical Research, Regulatory Affairs, and Medical Writing. The positions offer remote and hybrid work options across India, including Gurugram.

With strong demand for professionals skilled in Veeva Vault, eTMF, medical writing, centralized monitoring, and clinical data review, these openings are attracting significant attention in the pharmaceutical and CRO industry.

1. Medical Writer II (MLR Reviewer + Veeva) – Syneos Health

Job Overview

• Company: Syneos Health
• Role: Medical Writer II (MLR Reviewer + Veeva)
• Location: India Remote / Gurugram Hybrid
• Job Type: Full-Time
• Experience Required: Mid-Level Experienced Professionals
• Department: Clinical Solutions / Medical Writing
• Posted: Yesterday

Key Responsibilities

Candidates selected for the Medical Writer II role will:

• Lead and mentor junior medical writers on complex projects
• Prepare scientific documents including:
  • Clinical manuscripts
  • Abstracts
  • Posters
  • Oral presentations
• Perform literature searches and data interpretation
• Review statistical analysis plans and TFL specifications
• Coordinate with biostatistics, regulatory affairs, and medical affairs teams
• Ensure compliance with SOPs, journal guidelines, and regulatory standards
• Use tools such as:
  • Veeva Vault PromoMats
  • Datavision
  • GraphPad Prism
  • Adobe Illustrator
• Conduct scientific accuracy and branding reviews

Preferred Qualifications

• PharmD / M.Pharm / PhD / Life Sciences background
• Experience in medical writing and publication planning
• Strong understanding of Veeva Vault PromoMats
• Knowledge of publication compliance and scientific communication
• Excellent English writing and communication skills

Salary Expectation

Expected salary for this role in India can range between:

• ₹10 LPA – ₹18 LPA depending on experience and publication expertise.

2. Medical Writer I (Junior Project Specialist – 1 Year Contract)

Job Overview

• Company: Syneos Health
• Role: Medical Writer I (Junior Project Specialist)
• Location: Remote India / Gurugram Hybrid
• Employment Type: Full-Time Contract (1 Year)
• Experience: Freshers to 2 Years
• Domain: Veeva RIM / eTMF Operations

Key Responsibilities

The selected candidates will work extensively with Veeva RIM and eTMF systems.

Responsibilities include:

• eTMF filing and document management
• Managing document uploads/downloads in Veeva
• Maintaining metadata quality and naming conventions
• Supporting GxP-compliant documentation processes
• Filing documents related to:
  • Early Access Programs
  • Observational Studies
  • Non-Interventional Studies
• Supporting digital archiving and regulatory documentation
• Collaborating with client stakeholders and project teams
• Ensuring project timelines and milestone completion

Skills Required

• Knowledge of:
  • Veeva RIM
  • eTMF
  • GxP guidelines
  • Regulatory documentation
• Strong attention to detail
• Good communication and coordination skills
• Ability to work in remote cross-functional teams

Eligibility Criteria

Candidates from the following backgrounds may apply:

• B.Pharm
• M.Pharm
• PharmD
• Life Sciences
• Clinical Research
• Biotechnology

Salary Range

• ₹4.5 LPA – ₹7.5 LPA (estimated for contract-based junior medical writing/eTMF operations roles)

3. Clinical Data Reviewer (Centralized Monitoring / Clinical Scientist Support)

Job Overview

• Company: Syneos Health
• Role: Clinical Data Reviewer
• Location: Remote – India
• Experience: 8+ Years
• Industry: Clinical Data Management / Centralized Monitoring

Major Responsibilities

Professionals hired for this role will:

• Review clinical and medical trial data
• Identify inconsistencies and issue data queries
• Conduct centralized monitoring activities
• Review:
  • AE/SAE data
  • Concomitant medications
  • Eligibility criteria
  • Lab data
  • Efficacy endpoints
• Collaborate with:
  • Clinical Scientists
  • Study Medical Directors
  • Data Management Teams
• Support audit readiness and database lock activities
• Participate in data review meetings and data dissemination activities

Required Qualifications

Educational backgrounds accepted:

• MBBS
• MD
• BDS
• BHMS
• BAMS
• PharmD
• PhD

Experience requirements:

• 8+ years in clinical data review or centralized monitoring
• Strong experience with:
  • MedDRA
  • WHO Drug Dictionary
  • EDC systems
  • ARGUS
  • RShiny visualizations
  • Query management

Estimated Salary

• ₹18 LPA – ₹30 LPA depending on therapeutic expertise and sponsor-facing experience.

Why Join Syneos Health?

Benefits Offered

Syneos Health provides:

• Remote and hybrid work flexibility
• Global CRO exposure
• Career progression programs
• Technical and therapeutic area training
• Inclusive work culture
• Opportunities to work on FDA and EMA regulated studies
• Exposure to advanced clinical systems and publication platforms

The company states that over the past 5 years, it has contributed to:

• 94% of Novel FDA Approved Drugs
• 95% of EMA Authorized Products
• 200+ studies across 73,000+ sites globally

How to Apply

Application Link For Medical Writer II (MLR Reviewer +Veeva)

Application Link For Clinical Data Reviewer(Centralized Monitoring/Clinical Scientist Support)