Clinical Trials-Reputed Pharmacy Industry-Chennai, Tamil Nadu, India

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.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.2.Creating and implementing study-specific clinical monitoring tools and documents. 3.Creating and overseeing trial budget. 4.Identifying, enlisting and choosing sites, and coordinating site...

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....

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....

JOB DETAILS 1.Maintain records and send reports including tour programs, daily, weekly reports, expense claims, orders and information about competitive products and activities.2.Carrying out one-on-one discussions and meetings with doctors and pharmacists in order to convince them about our products & collect information on healthcare supplies. 3.Candidate...

JOB DETAILS 1.Maintain records and send reports including tour programs, daily, weekly reports, expense claims, orders and information about competitive products and activities.2.Carrying out one-on-one discussions and meetings with doctors and pharmacists in order to convince them about our products & collect information on healthcare supplies. 3.Candidate...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians) 3.setting up and disbanding trial study centres 4.designing trial materials and supplying study centres with sufficient quantities 5.providing clinicians with instructions on how to conduct the trials 6.collecting and...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians) 3.setting up and disbanding trial study centres 4.designing trial materials and supplying study centres with sufficient quantities 5.providing clinicians with instructions on how to conduct the trials 6.collecting and...