Novartis is indeed recognized as a leading pharmaceutical company with a reputation for having an exciting product pipeline. The company has a strong commitment to innovation and the development of new medicines to address unmet medical needs. This dedication is driven by a diverse and talented workforce that contributes to the success of Novartis.
As an employer, Novartis strives to provide a rewarding work environment for its employees. The company values performance-driven individuals who are passionate about making a difference in the healthcare industry. Novartis offers opportunities for personal and professional growth, encouraging employees to develop their skills and expertise.
Working at Novartis can be fulfilling due to the potential impact on global health and the opportunity to contribute to the development of groundbreaking therapies. The company is committed to creating an inclusive and collaborative culture where employees can thrive and make meaningful contributions.
Position: Scientific Writer II
Job Description: As a Scientific Writer II, your responsibilities will include:
- Writing and/or editing high-quality clinical and safety documents, such as non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Clinical Trial Registration Documents, or Patient Narratives, under guidance.
- Acting as a documentation consultant in Clinical Trial Teams (CTTs) to ensure compliance with internal company standards and external regulatory guidelines.
- Serving as a liaison between CTTs and publishing teams to ensure timely delivery of final documents for publishing.
- Reporting technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt.
- Distributing marketing samples (if applicable).
- Timely preparation of publications to meet regulatory requirements for the publication of clinical trial results, increase customer awareness of company products, and support marketing activities.
- Life-science degree or equivalent B.Sc./equivalent with 4 years of Clinical Research (CR) experience.
- M.Sc./M.Pharm with 2 years of CR experience.
- Doctoral degree
- Qualification in Medical Sciences (MBBS/MD/equivalent)
- PhD with 1 year of CR experience
- MBBS/equivalent with 1 year of CR experience
- Excellent written and oral English skills.
- Experience: 4 years
- Qualification: M.Pharm, MSc, BSc, PhD, MBBS/MD/equivalent
- Location: Hyderabad, AP
- Industry Type: Pharma
- Functional Area: Research & Development
- End Date: 30th July 2023
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