Job Description
Roles and Responsibilities
- Acts as a lead medical writer on programs and numerous individual studies at a moderate to complex level.
- Provides scientific and medical writing consultancy to clients and internal colleagues at a complex level.
- Leads project teams in drafting report specifications, medical writing, and coordination of regulatory submissions and data analysis.
- Manages all aspects of the medical writing function.
- Serves as an active mentor to one or more junior staff members.
- Develops and implements training for medical writers in areas of expertise.
- May represents the medical writing group with new or current clients in client forums
Desired Candidate Profile
- Understands regulatory submissions requirements and clinical study report guidelines in host country.
- Exhibits excellent written and oral communication and presentation skills.
- 7 - 10 years for Medical writing experience
- Bachelors degree in scientific, health-related field
- Demonstrates strong ability in developing pharmaceutical drugs for human use.
- Shows substantial skill in writing technical sections of regulatory documents, clinical study reports, poster presentations, or manuscripts for publication in a scientific journal.
Interested candidates kindly share updated CV to ku*********n@pr**s.com
Job Classification
Industry: Pharma, Biotech, Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology,
Role Category: R&D
Role: R&D
Employement Type: Full time
Education
Under Graduation: Any Graduate in Any Specialization
Post Graduation: MBA/PGDM in Any Specialization
Contact Details:
Company: Pharmaceutical
Address: A603,,The Qube,M.V.Road,Marol, , , MUMBAI, Maharashtra, India
Location(s): Hyderabad
Keyskills:
Clinical study Reports
Informed consent forms
Medical Writing
Protocol Writing
Narrative Writing