Job Description (Posting). (We don’t have “Medical Writer” designation in the drop down list so selected “Clinical Trial Specialist”)
Job Title: Medical Writer
POSITION SUMMARY
• To develop, review and revise clinical study reports, investigator’s brochure and protocols of drug trials
• To develop, review and revise clinical evidence summaries (CES)/ clinical evaluation reports (CER) and post marketing surveillance reports of Medical Devices
• To perform tasks including researching medical information, summarizing data from clinical studies, consulting, editing statistical and clinical reports
• Review of Medical journals and technical reports
• Working closely with doctors, researchers and various people in Medical services to provide information which is accurate and easy for others to understand
RESPONSIBILITIES
• Developing protocol, investigator’s brochure, informed consent form, interim study reports and clinical study reports
• Developing clinical investigation protocols, clinical evidence
Experience 3-5 Years
Qualification BSc, MBBS, MSc, Phd, BDS, B.Pharma, M.Pharma, BS, Medical Science, Ph.D/Doctorate, BPT, Bach of Homoeopathic Medicine & Surgery, M.Sc
No. of Positions 3
Skill (Primary) Domain Competencies (BSERV )-Healthcare-Operations Management
Removal Date 30-Aug-2014
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Job Title: Medical Writer
POSITION SUMMARY
• To develop, review and revise clinical study reports, investigator’s brochure and protocols of drug trials
• To develop, review and revise clinical evidence summaries (CES)/ clinical evaluation reports (CER) and post marketing surveillance reports of Medical Devices
• To perform tasks including researching medical information, summarizing data from clinical studies, consulting, editing statistical and clinical reports
• Review of Medical journals and technical reports
• Working closely with doctors, researchers and various people in Medical services to provide information which is accurate and easy for others to understand
RESPONSIBILITIES
• Developing protocol, investigator’s brochure, informed consent form, interim study reports and clinical study reports
• Developing clinical investigation protocols, clinical evidence
Experience 3-5 Years
Qualification BSc, MBBS, MSc, Phd, BDS, B.Pharma, M.Pharma, BS, Medical Science, Ph.D/Doctorate, BPT, Bach of Homoeopathic Medicine & Surgery, M.Sc
No. of Positions 3
Skill (Primary) Domain Competencies (BSERV )-Healthcare-Operations Management
Removal Date 30-Aug-2014
Read More
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