Scientific Writing

2 months ago


Mumbai, India NMS Consultant Full time

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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