Associate Medical Writer

2+ years

Not Disclosed

Bangalore

10 Dec. 16, 2024

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Associate Medical Writer
Location: Bangalore, India
Category: Medical Affairs
Department: Global Medical Affairs – Global Business Services (GMA-GBS)

Job Description:

Are you passionate about medical writing and eager to contribute to life-changing scientific activities on a global scale? Novo Nordisk is seeking an Associate Medical Writer to join our Global Medical Affairs unit. This role offers you the opportunity to participate in crucial global initiatives, working with cross-functional teams to drive the development of study protocols, reports, and medical documents that play a pivotal role in advancing healthcare solutions.

As an Associate Medical Writer, you will:

Moderate discussions with study groups to develop study protocols and reports.
Facilitate document-review meetings and provide comments on consolidated documents.
Coordinate clinical document version reviews and approval processes, ensuring audit-preparedness.
Conduct literature searches and prepare summaries of systematic reviews.
Contribute to internal and external marketing/medical activities, including expert meetings and conferences.
Maintain up-to-date knowledge within relevant therapeutic areas (e.g., diabetes, obesity, MASH).
Collaborate with global medical directors to prepare medical writing tasks such as study protocols, non-interventional study reports, and investigator’s brochures.
Develop abstracts, congress posters, and presentations for global events.
Ensure compliance with SOPs, timelines, regulatory requirements, and guidelines.

Qualifications:

A degree in a relevant field (e.g., life sciences, medical, pharmaceutical).
2+ years of experience in medical writing, particularly in preparing study protocols, non-interventional study reports, and investigator’s brochures.
Strong understanding of real-world studies and therapeutic areas like diabetes, obesity, and MASH.
Ability to perform literature searches and prepare detailed summaries.
Experience in developing abstracts, congress posters, and presentations.
Excellent communication and collaboration skills.
Ability to ensure audit-preparedness and manage clinical document reviews and approval processes.
Experience in the pharmaceutical or healthcare industry.
Familiarity with regulatory requirements and guidelines.
Experience in process improvements and knowledge sharing.

About the Department:

The Global Medical Affairs – Bangalore (GMA-BLR) is an extension of the Global Medical Affairs unit in Denmark and is part of Global Business Services (GBS). This department plays a critical role in supporting global regions and affiliates in the ideation, execution, and lifecycle management of real-world studies, from protocol development to study conduct, data analysis, publications, and medical affairs activities.

Working at Novo Nordisk:

Novo Nordisk is a global leader in healthcare, with a legacy of over 100 years in transforming the lives of millions of people living with chronic diseases, particularly diabetes. With a rapidly growing global presence and a market cap placing us among the 20 most valuable companies, we strive to build a diverse, inclusive environment where all employees can thrive. Join us and be a part of something bigger—together, we’re life-changing.

How to Apply: Please upload your CV and motivational letter online by clicking Apply Now and following the instructions.

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