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Merck KGaA
Job Title – Document CoordinatorLocation: Bangalore - Electronic City About the RoleAs a Document Coordinator, you will support the Global Medical Writing Team to deliver its portfolio effectively and efficiently.Your role would require you to: Conduct quality review of clinical and regulatory documents including but not limited to Protocols, Clinical Study Reports, Briefing Books, Investigator Brochures, and Clinical Summary documents.Ability to work within a team in collaborative and supportive role Mentor and train the assigned new joiners/junior Document coordinatorsParticipate in meetings related to key MW, QC, and compliance activitiesCollaborate cross functionally for continuous improvement of for medical writing Who you are: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.Excellent written and spoken English (including medical terminology) and familiarity with AMA style guide.Knowledge of Clinical and RegulatorydocumentsPharmaceutical 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 adapt 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 is at the forefront of all our activities. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.
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