Syneos Health Hiring Junior Project Specialist I Remote

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Syneos Health Hiring Junior Project Specialist I Remote

🏢 Syneos Health

🌍 Remote / Gurugram

✍️ Medical Writing

📂 eTMF / Veeva

🎓 Freshers Eligible

Syneos Health is hiring for Medical Writer I (Junior Project Specialist) role for Remote India & Gurugram locations.

This opportunity is ideal for candidates interested in Medical Writing, Regulatory Documentation, eTMF Management, Veeva RIM Systems, Clinical Operations, and Global Regulatory Workflows.

📋 Job Overview

Position: Medical Writer I (Junior Project Specialist)
Company: Syneos Health
Location: Remote India & Gurugram
Employment Type: Full-Time
Contract Duration: 1 Year
Department: Clinical Solutions
Industry: Clinical Research / Regulatory Affairs / Medical Writing
Work Mode: Remote / Hybrid
Experience: Freshers & Experienced Candidates

💰 Estimated Salary: ₹4 – ₹7 LPA

📌 Key Responsibilities

Support compliant document filing within Veeva RIM systems
Manage eTMF filing activities following GxP guidelines
Upload and categorize regulatory and clinical documents
Maintain document quality and metadata accuracy
Maintain electronic archiving standards and naming conventions
Support observational studies and Early Access Programs
Coordinate with stakeholders and internal project teams
Monitor timelines, deliverables, and submission deadlines
Participate in client-facing and internal meetings
Support SOPs, workflows, and process improvement activities
Maintain FDA, EMA, and global regulatory compliance standards

🎓 Eligibility Criteria

📚 Educational Qualification

B.Pharm
M.Pharm
Pharm.D
MSc Life Sciences
Biotechnology
Biochemistry
Clinical Research
Other Healthcare or Life Sciences Degrees

💡 Preferred Skills

Knowledge of Veeva RIM or eTMF systems
Understanding of GxP guidelines
Strong documentation and file management skills
Attention to detail
Communication and stakeholder coordination abilities
Basic understanding of regulatory documentation workflows

🌍 Why Join Syneos Health?

Remote work flexibility
Exposure to global pharmaceutical and clinical projects
Training in clinical research and regulatory systems
Career growth in medical writing and regulatory operations
Collaborative and inclusive work culture
Opportunity to work with leading healthcare clients worldwide

🌟 Company Highlights

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

💡 Interview Tips

Revise GxP and regulatory documentation basics
Understand eTMF and Veeva RIM workflows
Prepare medical writing and file management concepts
Practice communication and stakeholder coordination questions
Be ready to discuss clinical research basics
Highlight attention to detail and documentation skills

📄 Resume Tips

Highlight clinical research, documentation, or regulatory internships clearly
Mention Veeva, eTMF, MS Office, or medical writing exposure if available
Add certifications related to Pharmacovigilance, Clinical Research, or Regulatory Affairs
Use ATS-friendly resume format with proper keywords
Showcase communication, documentation, and coordination skills
Include projects related to healthcare, clinical trials, or research
Keep resume concise, professional, and error-free
Focus on compliance, attention to detail, and teamwork abilities

🧩 Fun Learning & Career Growth

Improve your healthcare knowledge and analytical skills with our quizzes and puzzles.

🚀 Apply Now

📌 Note Before You Apply:

Kindly read the complete job description carefully before applying. Ensure your documentation skills, regulatory understanding, and clinical research knowledge align with the role requirements before proceeding.

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