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CLINICA Research

1 Years +

Navi Mumbai

B.Pharm, M.Pharm, Pharm.D

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Work/Life Balance

Time management

challenging projects

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CLINICA Research Solutions LLP is a leading Clinical Research Organization (CRO) based in Navi Mumbai, Maharashtra. We specialize in providing comprehensive services to the pharmaceutical, biotechnology, and medical device industries. As we continue to grow, we are looking to expand our talented team with an experienced Medical Writer who will contribute to the success of our clinical research projects.

Responsibilities in Job
As a Medical Writer at CLINICA Research Solutions LLP, your role will involve:

  • Preparation of Clinical Documents: You will assist in the preparation of clinical study reports, protocols, informed consent forms, and other regulatory submissions that adhere to industry standards.
  • Non-regulatory Medical Writing: Your role will also involve assisting in the creation of non-regulatory medical documents for internal and external communication.
  • Collaboration: You will collaborate with cross-functional teams, including medical, clinical, and regulatory affairs, to ensure that all documents are accurate and compliant with regulatory standards.
  • Clear Communication: A key responsibility will be to communicate complex medical and scientific information in a clear, concise, and accessible manner.

Qualification
To qualify for this role, you must have:

  • Minimum of 1 Year of Experience: You should have at least one year of experience as a Medical Writer in a clinical research or pharmaceutical setting. Freshers need not apply.
  • Educational Background: A degree in Life Sciences, Pharmacy, or a related field is preferred.

Skills

  • Medical Writing Skills: Strong command of writing clear and accurate clinical documents.
  • Attention to Detail: Ability to meticulously review and edit clinical documents to ensure accuracy.
  • Communication Skills: Excellent written and verbal communication skills for conveying complex scientific information in a user-friendly manner.
  • Regulatory Knowledge: Understanding of regulatory standards, guidelines, and the drug development process is a plus.

How to Apply
If you’re an experienced Medical Writer and are ready to contribute to an innovative and expanding organization, we’d love to hear from you!

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