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Cognizant
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Medical Writer

Medical Writer

Cognizant

4 - 8 years

0 Lacs

chennai tamil nadu

Posted:1 day ago| Platform: Shine logo

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Skills Required

content writing data interpretation medical communications clinical trial knowledge analytical thinking

Work Mode

On-site

Job Type

Full Time

Job Description

You will be responsible for writing and editing high-quality regulatory submission documents such as CSR, Protocol, and Investigator Brochure. Your role will involve communicating with medical experts, patients, or representatives from pharmaceutical companies to gather medical resources and verifications. Collaboration and verification of data with the Client's internal study teams will be essential. It is important to thoroughly study reports and cross-check information for completeness, as well as conduct frequent quality control checks on each submission. Ensuring that documents adhere to the organization's writing guidelines and are appropriately stored and organized is also a key aspect of the role. To qualify for this position, you should have a Bachelors or Masters Degree in Life science, biology, medical science, or a related medical field. Additionally, you must have 4-6 years of content writing experience in the healthcare or pharmaceutical industry. Experience in managing multiple content and studies at different stages, knowledge of medical terminologies and jargon, and excellent verbal communication skills are also required. The ideal candidate will possess skills such as clinical trial knowledge, the ability to understand clinical data and create study documents like CSR, Protocol, and Investigator Brochure. Broad and in-depth expertise in clinical concepts and regulations, proficiency in content writing, analytical thinking, and data interpretation, as well as strong medical communications and great attention to detail are essential. This position is based in Chennai, Pune, Hyderabad, or Bangalore.,

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Medical Writer