Clinical Research associate-Reputed Medical

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

**Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe.** **Salary**: ₹500,000.00 - ₹600,000.00 per year **Benefits**: - Health insurance Schedule: - Day...

Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe. Your responsibilities include, but are not limited to: - Closely collaborates with the Trial Monitoring Organisation...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee...

**MakroCare** is an Expert Strategic Development and Commercialization Global Partner for Pharmaceutical,Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a NewDimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,Medical/Scientific Support and Emerging Region Expansion **Job...

Develop and outline the purpose and methodology of trials - Present trial protocols to a leading committee - Identify and assess the suitability of facilities to be used at a clinical trial site - Document site visits, issue reports, and follow-up letters to a site - Visit trial sites on regular basis to conduct clinical trials on new drugs or medical...

Clinical Research Coordinator (Freshers Only)Location: [Insert City / Across India – Hybrid/On-site]Organization: Clinogenesis Research OrganizationDepartment: Clinical OperationsEmployment Type: Full-TimeAbout ClinogenesisClinogenesis Research Organization is a growing, innovation-driven CRO committed to excellence in clinical research and data-driven...