Course Info
Clinical and Regulatory Medical Writing
Course objective:
In this course, you will learn how to author clinical study reports (CSRs), clinical study protocols, narratives, and CTD modules related to Phase I-III studies in the pharmaceutical industry. The course is suitable for MDs, PhDs, and PharmDs looking to transition into a medical writing role in the pharmaceutical industry. The lessons focus on the therapeutic areas of immuno-oncology, infectious disease, and autoimmunity.
$1,995.00
Course highlights:
Instructor: Dr. Fatima Larry
Duration: 6 Weeks
Level: Beginner/Intermediate
Live, virtual, and direct interactions with the instructor
Hands-on document authoring and feedback
Exclusively for individuals seriously pursuing a senior-level clinical or medical writing role in the pharmaceutical or biotechnology industry