10+ years\' experience in regulatory medical writing. Experience in authoring protocols, clinical study reports, investigators brochures, informed consent forms, summary documents, etc. Experience in multiple therapeutic areas, including but not limited to vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders, gastrointestinal disorders, infectious diseases, mental health, neurology oncology, etc. Strong communication and interpersonal skills. Bachelors/advanced degree or equivalent education/degree in life sciences/healthcare. Experience from the pharmaceutical /CRO industry. Ability to work independently and lead projects. Strong analytical skills. Commitment to highest quality outputs, including high attention to detail. Ability to manage variable workload. Prior experience in Regulatory Medical writing would be desirable.
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