Medical Writer Jobs | Syneos is Hiring | Apply Now
Looking for medical writer jobs in the life sciences industry? Syneos Health is hiring a Medical Writer I (Project Specialist) for a remote role based in Pune, offering an excellent opportunity for candidates with clinical research and document management experience. This Syneos career opportunity is ideal for professionals interested in clinical research documentation, regulatory writing, and pharmaceutical communication within global clinical trials.
- Job Role: Medical Writer I (Project Specialist)
- Job Location: Pune / Remote
- Job Type: Full-time
About the Company
Syneos Health is a leading global biopharmaceutical solutions organization operating across 110 countries with more than 29,000 employees. The company supports pharmaceutical and biotechnology organizations in clinical development, regulatory affairs, and commercialization of therapies. Over the past few years, the organization has contributed to 94% of novel FDA-approved drugs and numerous global clinical trials, making it one of the most influential CROs in the life sciences sector.
Key Responsibilities
- Manage and organize clinical documents within Veeva systems
- Perform eTMF filing and documentation classification
- Ensure compliance with GxP guidelines and regulatory standards
- Maintain document integrity and quality before submission
- Track and manage project documentation timelines
- Collaborate with clinical research and regulatory teams
- Support development and improvement of workflows and SOPs
Qualifications
- Bachelor’s degree in the life sciences with relevant scientific and/or medical knowledge and expertise; or equivalent experience.
- 1–2 years of experience in ETMF filing and Document management systems.
Skills
- Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint).
- Exceptional attention to detail with strong organizational abilities and a service-oriented mindset.
- Fluent in written, spoken, and reading English, with the capacity to multitask and perform effectively in high-pressure environments.
- Excellent grammatical and communication skills, both written and oral.
- Ability to work with minimal supervision on multiple assignments with set deadlines.
- Knowledge of FDA and EU requirements, ICH regulations, and ISO standards as applicable to regulatory documents preferred.
If you are looking for medical writer jobs in clinical research, this Syneos career opportunity can help you build expertise in regulatory writing, clinical documentation, and life sciences communication. With global exposure and experience in clinical trial documentation, this life sciences job can open doors to advanced careers in medical writing, regulatory affairs, and clinical research.
