Medical Writer Job – B.Pharm & M Pharm at Cliantha Research
Department : Consumer Research
Basic qualification required : B.Pharm / M. Pharm, M.Sc
Experience : 2 – 6 Years
Job Description
• Preparation of Protocols, Informed Consent Forms, Case Report Forms, and other protocol related documents as per applicable regulatory requirements in consultation with Group In-charge, Principal Investigator, Biostatistician, Analytical Investigator, and Head of the department.
• Coordination with study personnel and other departments for protocol related issues for finalization of protocol.
• Approval of protocols from Ethics committee in consultation with Principal Investigator and Sponsor.
• Responsible for updating the protocol related concerns to investigator(s), sponsor and IEC
• Preparation and revision of related SOPs.
• Conforms to training schedule for own position and maintains awareness of SOPs contents according to company requirements.
• Stays current with the ongoing changes in the pharmaceutical regulatory environment, i.e. FDA, GCPs, GLPs, etc
Location : Ahmedabad
Last date :15th August, 2023