Scientific Writing
2 months ago
From 5 to 10 year(s) of experience
₹ Not Disclosed by Recruiter
- Mumbai (All Areas)
**Roles and Responsibilities**
1. Drafting and reviewing of protocol synopsis, clinical study protocol, investigators brochure,
consent documents, patient diary, etc of Phase 3 or Phase 4 clinical trial.
2. Drafting consolidated clinical study report as well as centre-wise study reports
3. Drafting manuscripts for publications
4. Drafting write-ups and preparing presentations for publications, scientific meetings etc
- Key Skills
- DraftingClinical ResearchClinical TrialsScientific Writing
- clinical studyreportsMedical WritingPharma
- Skills highlighted with ‘‘ are preferred keyskills
Education
- PG:_M.Pharma in Any Specialization
**Company Profile**:
NMS Consultant
Leading Pharmaceutical Company
Company Info
**Salary**:
Not Disclosed by Recruiter
Industry:
Pharmaceutical & Life Sciences
Department:
Healthcare & Life Sciences
Role Category:
Healthcare & Life Sciences - Other
Role:
Healthcare & Life Sciences - Other
Employment Type:
Full Time, Permanent
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