Syneos Health, a leading fully integrated biopharmaceutical solutions organization, is hiring for Statistical Programmer I (Pune, Office-Based) and Medical Writer II (India, Home-Based). If you’re looking for exciting career opportunities in clinical research, biostatistics, and medical writing, this could be your chance to join a global team dedicated to accelerating drug development and improving patient outcomes.
1. Statistical Programmer I – Pune (Office-Based)
Job ID: 25002281
Experience Required: 6 months to 2 years
Location: Pune, India (Office-Based)
Job Description
As a Statistical Programmer I at Syneos Health, you will:
- Use SAS or other statistical software to generate summary tables, data listings, graphs, and derived datasets.
- Perform QC of outputs and ensure compliance with statistical analysis plans (SAP).
- Conduct validation programming and collaborate with biostatisticians to resolve discrepancies.
- Maintain well-organized project documentation for inspection readiness.
- Manage multiple projects efficiently while adhering to regulatory guidelines (ICH, SOPs, WIs).
- Communicate effectively with project teams and contribute to problem-solving.
Qualifications
- Bachelor’s degree in a scientific or statistical discipline (or equivalent experience).
- Proficiency in SAS programming (experience in clinical trials preferred).
- Strong attention to detail, critical thinking, and problem-solving skills.
- Good understanding of clinical trial data and regulatory requirements.
- Excellent English communication skills (written & verbal).
Why Join Syneos Health?
- Career growth & development with technical and therapeutic training.
- Total Self culture – A diverse and inclusive workplace where authenticity is valued.
- Work with 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products.
2. Medical Writer II – India (Home-Based)
Job ID: 24006743
Experience Required: 3+ years in Medical Writing
Location: India (Home-Based)
Job Description
As a Medical Writer II, you will:
- Develop and edit clinical study documents, including:
- Protocols, Clinical Study Reports (CSRs), Investigator Brochures (IBs), Patient Narratives, and Annual Reports.
- Review statistical analysis plans (SAPs) and ensure compliance with ICH-E3 guidelines.
- Lead client calls independently, schedule meetings, and manage documentation (MOMs).
- Perform peer reviews and ensure scientific accuracy, clarity, and consistency.
- Stay updated with regulatory guidelines and industry best practices.
Qualifications
- 3+ years of medical writing experience in clinical research.
- Strong scientific writing, editing, and proofreading skills.
- Familiarity with clinical trial operations & regulatory submissions.
- Proficiency in Microsoft Word, Excel, PowerPoint.
- Ability to interpret clinical data and present complex information clearly.
Why Join Syneos Health?
- Mentorship & leadership opportunities for career progression.
- Flexible home-based role with minimal travel (<25%).
- Work on global clinical trials with a diverse and collaborative team.
About Syneos Health
Syneos Health is a top biopharmaceutical solutions company with 29,000 employees across 110 countries. Over the past 5 years, they have contributed to:
- 94% of all Novel FDA Approved Drugs
- 95% of EMA Authorized Products
- 200+ Studies across 73,000 Sites & 675,000+ Trial Patients
Their Total Self culture promotes diversity, inclusion, and professional growth, making it a great place to work.
How to Apply?
Application Link For Statistical Programmer I – Pune (Office-Based)
Application Link For Medical Writer II – India (Home-Based)
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