Jobs For Clinical Research Associate-Medical

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.Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.Review...

JOB DETAILS1) 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...

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...

JOB DETAILS1) 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...

**JOB SUMMARY / ROLE**: The Clinical Research Coordinator will plan, direct, or coordinate INPHOG clinical research projects, and will evaluate and analyse clinical data. **JOB RESPONSIBILITIES**: - To facilitate and coordinate the all daily INPHOG clinical research trial activities for sponsored & academic studies, for assigned projects. - To review and...

**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...

JOB DETAILS1) 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 DETAILS1) 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 Summary: We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory...

Job Summary: We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory...

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...

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...

387199BR **Associate Medical Expert**: India **About the role** Associate Medical Expert Location - Hyderabad #LI Hybrid About the Role: The Associate Medical Expert will ensure the successful implementation and delivery of the Medical and Knowledge Solutions (MKS) scientific and medical services along the business colleagues’ requirements. He/ she is...

Apply for Clinical Research Associate, Career Progress Consultants in Hyderabad/ Secunderabad for 0 - 3 Year of Experience on

387199BRAssociate Medical Expert:IndiaAbout the roleAssociate Medical ExpertLocation - Hyderabad #LI HybridAbout the Role:The Associate Medical Expert will ensure the successful implementation and delivery of the Medical and Knowledge Solutions (MKS) scientific and medical services along the business colleagues' requirements. He/ she is expected to support...

Responsibilities Support CRAs with the setup monitoring and closeout of clinicaltrials in accordance with Good Clinical Practice (GCP) ICHguidelines and company SOPs. Assist in sitequalification initiation and monitoringvisits. Review and track clinical trialdocumentation ensuring accuracy andcompleteness. Collaborate with crossfunctionalteams to address...

We need young and engergitic with Qualification in B.Pharmay with 0 to 1 years experience with good communication skills, computer skills in MS office. **Job Types**: Full-time, Regular / Permanent, Fresher **Salary**: ₹11,000.00 - ₹13,000.00 per month Schedule: - Day shift - Flexible shift Supplemental pay types: - Overtime pay - Performance...

108,000 people reimagining medicine for more than 799 million people globally. Be part of this journey by representing a group that delivers medical communication solutions across multiple franchises, business units and affiliates. Our services and customized solutions enhance the reach of clinical data about relevant therapeutic advancements and supports in...