Scientific Writing (clinical Research)
Year Mumbai, Maharashtra, India
Job Description
From 5 to 10 year(s) of experience
9 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 5. Provide necessary support for preparing regulatory dossier for application of clinical trials
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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Job Detail
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Job IdJD3016611
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationMumbai, Maharashtra, India
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EducationNot mentioned
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ExperienceYear