Research Analyst (Medical Writer)

Role & responsibilities:

Clinical Protocol Preparation

• Carrying Literature survey to provide scientific inputs for protocols and study Reports.
• Preparation and Compilation of study proposal Synopsis for Pharmacodynamics, Pharmacokinetic and BA/BE studies.
• Responsible for research, create, edit and coordinate the preparation and review of clinical study protocols.
• Provide guidance and scientific direction for creative designs and input into study protocols as appropriate.
• Responsible for development and delivery of scientifically accurate protocol content that is aligned with study objectives and meets the specification of the sponsor.
• Identification and development of clinical study designs as per current global customer requirements.

Pharmacy

• Responsible for receipt of drug for Bioavailability/Bioequivalence and Clinical Trial Studies.
• Maintenance of drug products in the pharmacy as per the product specific storage condition.
• Responsible for dispensing the investigational drug products as per the randomization schedule for Bioavailability/Bioequivalence and Clinical Trial Studies.
• Responsible for archival and/ or disposition of investigational drug products as per the protocols and/or sponsor requirement.
• Review procedures for pharmacy operations.

Preferred candidate profile can send to email:hr@qpsbioserve.com

Perks and benefits: Nil