About Company
Wockhardt is a global pharmaceutical and biotechnology organization, providing affordable, high-quality medicines for a healthier world. It is India’s leading research-based global healthcare enterprise with relevance in the fields of Pharmaceuticals, Biotechnology and a chain of advanced Super Specialty Hospitals. Wockhardt is a true Indian Multi-National Company with a multi-ethnic workforce of 3000 Wockhardt Associates from 21 different nationalities globally. It has 3 research centers and 12 manufacturing plants, with businesses ranging from the manufacture and marketing of Pharmaceutical and Bio-pharmaceutical formulations, Active Pharmaceutical Ingredients (APIs) and Vaccines. Headquartered in Mumbai, India, Wockhardt has full-fledged operations in the USA, UK, Ireland and France.
Job Role: Medical Writer
Job Overview:
As a Medical Writer at Wockhardt Pharma, you will be responsible for creating high-quality, scientifically accurate medical documents, including clinical study reports, regulatory submissions, publications, and educational materials. This role demands adherence to relevant guidelines and standards, along with a deep understanding of the therapeutic areas and products within the Wockhardt portfolio.
Key Responsibilities:
Document Development:
- Draft and revise clinical study reports (CSRs), protocols, Investigator Brochures, and safety narratives.
- Write and edit scientific manuscripts for peer-reviewed journals.
- Develop patient information materials and healthcare professional educational content.
- Prepare presentations and summaries of clinical data for internal and external stakeholders
Data Analysis and Interpretation:
- Analyze clinical trial data to identify key findings and translate them into clear, concise reports.
- Interpret complex scientific information to ensure accurate representation in medical documents.
- Collaborate with clinical research teams to understand study designs and objectives.
Compliance and Quality Assurance:
- Adhere to regulatory guidelines (ICH, FDA, etc.) and internal SOPs for medical writing.
- Review and edit documents thoroughly for accuracy, consistency, and clarity.
- Deliver high-quality documents within project timelines.Therapeutic Area Expertise:
- Develop and maintain expertise in assigned therapeutic areas, including disease states and treatment options.
- Stay updated on scientific advancements and regulatory requirements.
Collaboration:
- Work closely with cross-functional teams, including clinical research, regulatory affairs, marketing, and project management, to align on medical writing strategies.
- Provide expert medical writing support and contribute to project planning and execution.
Qualifications:
- Education:
- A MBBS, MD Pharm. or Ph.D. in Pharmacology, Clinical Research, Life Sciences, or a related field is preferred.
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Wockhardt
