- Job Description:
- Write and edit high-quality regulatory submission documents like CSR, Protocol, Investigator’ Brochure etc.
- Communicate with medical experts, patients, or representatives from pharmaceutical companies for medical resources and verifications
- Collaborate and verify data with Client’s internal study teams
- Thoroughly study reports and cross-check information for completeness
- Conduct frequent and thorough quality control checks on each submission
- Ensure that documents adheres to the organization’s writing guidelines, and are appropriately stored and organized
- Write and edit high-quality regulatory submission documents like CSR, Protocol, Investigator’ Brochure etc.
- Qualifications:
- A Bachelor’s or Master’s Degree in Life science, biology, medical science, or any related medical field
- 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
- Excellent verbal communication skills
- A Bachelor’s or Master’s Degree in Life science, biology, medical science, or any related medical field
- Skills:
- Clinical Trial knowledge, ability to understand Clinical data and create Study documents like CSR, Protocol, Investigator’ Brochure etc.
- Broad & In-Depth Expertise in Clinical Concepts and Regulations
- Well versed in Content writing, Analytical Thinking and Data Interpretation
- Medical Communications and great attention to detail
- Location: Chennai/Pune/Hyderabad/Bangalore
- Clinical Trial knowledge, ability to understand Clinical data and create Study documents like CSR, Protocol, Investigator’ Brochure etc.