Research Associate

Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries.

1. Ensure quality documents that objectively and accurately represent the clinical trial data

2. Ensure deliverables are met as per planned and documented guidelines and standard operating procedures

3. Assist with the supervision, plan and review variety of clinical study documents like clinical CTD modules, investigators brochures, clinical trial protocols, Informed consent form (ICF), electronic/paper case record form, clinical trial safety reports, regulatory submissions etc by performing literature search, organizing the information, critically examining and interpreting scientific.

4. Performing quality check review of the above documents

02-03 years of related experience

B. Pharm / M. Pharm