Merck MD Job as Document Coordinator in Bengaluru – MD/BDS/PhD Candidates
Are you a B.Pharm or M.Pharm graduate with a flair for regulatory writing and quality documentation? Join Merck Group in Bengaluru as a Document Coordinator and become a part of a global medical writing team. This is your chance to support critical healthcare innovations while working in a collaborative and diverse environment.
Welcome to Merck Group
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
- Job Title – Document Coordinator
- Location – Bangalore – Electronic City
- Job ID: 286857
About the Role
As a Document Coordinator, you will support the Global Medical Writing Team in delivering its portfolio effectively and efficiently.
- Conduct quality review of clinical and regulatory documents, including but not limited to Protocols, Clinical Study Reports, Briefing Books, Investigational New Drug (IND) documents, and Clinical Summary documents.
- Ability to work within a team in a collaborative and supportive role
- Mentor and train the assigned new joiners/junior Document coordinators
- Participate in meetings related to key MW, QC, and compliance activities
- Collaborate cross-functionally for continuous improvement in medical writing
Who you are
Graduate or postgraduate 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.
- Excellent written and spoken English (including medical terminology) and familiarity with AMA style guide.
- Knowledge of Clinical and Regulatory documents
- Pharmaceutical industry experience (2-5 years related experience in a medical or other relevant pharmaceutical industry experience combined with scientific and regulatory knowledge) required.
- Knowledge of ICH/Good Clinical Practices, CTD guidance.
- A flexible attitude with respect to work assignments and new learning; readily adapts to changes
We are an equal opportunity employer that values workforce diversity. We want everyone to be able to bring their best self to work every day, which is why equality and inclusion are at the forefront of all our activities. We are dedicated to a non-discrimination policy in employment on any basis, including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.
What we offer: We are curious minds from various backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
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