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Require Principal Medical Writer at Merck - M.Pharm, B.Pharm, MSc Apply

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Require Principal Medical Writer at Merck

Our passion for  science and technology is what drives our around 63,000 employees in 65 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live. We are here for people at every step, helping to create, improve and prolong life. We deliver personalized treatments for serious diseases and enable people to achieve their dream of becoming parents. We empower the   scientific community. Our tools, services and digital platform make research simpler, more exact, and help deliver breakthroughs more quickly. Our solutions accelerate access to health by assuring tests are accurate and the medicine we take can be trusted. We are the company behind the companies, advancing digital living. Our science sits inside technologies that are changing the way we access, store, process, and display information.

Post : COMW-0 Principal Medical Writer

Job Description
• As a Principal Medical Writer you will play a pivotal role in leading the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional/local levels. 
• This includes independently preparing or overseeing the preparation of clinical and regulatory documents such as Protocols, Clinical Study Reports, Investigator Brochures, or Clinical Summary documents. You will also be responsible for supporting submissions for market approval/line extensions under minimal supervision. 
• In this role, you will oversee and coordinate other (external) writers assisting on documents under your responsibility, ensuring strict adherence to business objectives, company standards, as well as the organization of content, clarity of text and tables, overall consistency, and appropriate use of English language/grammar.
• You will represent the department as a subject-matter expert on clinical study teams, leading document-related meetings and reviewing study-related documents. 
• Additionally, you will ensure that all documents are produced according to agreed timelines, adhere to relevant SOPs, and meet the requirements of regulatory authorities and the company.
• Furthermore, you will play a proactive role in contributing to the development and implementation of Medical Writing best practices and process improvements.

Candidate Profile
•  Graduate or post graduate degree in BPharm/MPharm, PHD, BDS (Dental), BSC/MSC or equivalent job experience with comprehensive Medical Writing knowledge of theories, principles and concepts, MD/PhD or advanced science degree.
•  > 10 years experience in Pharma Industry (with 5 to 8 years of experience in Regulatory medical writing, including experience in postmarketing studies) 
•  Excellent written and spoken English (including medical terminology) and familiarity with AMA style guide


Additional Information
Experience : 5 to 8 years
Qualification : BPharm/MPharm, PHD, BDS (Dental), BSC/MSC 
Location : Bangalore
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th January 2025

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