Clinical Research Associate

JOB DETAILS 1 Performing routine data collection from patients,2 Verifying data sources, and reviewing regulatory documents/files to ensure that documents are in compliance with protocols, regulatory requirement3 SOPs (standard operating procedures), and are aligned with the Monitoring Plan.4 Some clinical research associates assist in reviewing study...

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 TitleClinical Research Associate - Biomedical Product Safety SpecialistA rewarding opportunity for a dedicated and detail-oriented professional to join our team as a Clinical Research Associate, specializing in biomedical product safety.About the JobKey Responsibilities:Review and align SOPs (standard operating procedures) and monitoring plans to ensure...

Job OpportunityWe are seeking an experienced professional to fill a Clinical Research Associate position. As a key member of our team, you will be responsible for overseeing clinical trials from initiation to closeout.Main Responsibilities:Create and present trial protocols to steering committees.Identify, evaluate, and establish trial sites for...

About the Role\ As a Clinical Research Associate, you will be responsible for conducting clinical trials and ensuring compliance with regulatory requirements. Your duties will include creating and writing trial protocols, identifying and establishing trial sites, training site staff, liaising with ethics committees, managing IP and trial materials, and...

Job Opportunity Clinical Research Associate Role: A Detailed OverviewThis role involves collaborating with the steering committee to create and present trial protocols. Identifying, evaluating, and establishing trial sites is a crucial aspect of this position. Additionally, training site staff on therapeutic areas, protocol requirements, and proper...

JOB DETAILS 1 To provide timely inputs in the protocol and Informed Consent (for e.g. dosing information, contraindications, warnings, precautions, adverse events, and drug interactions) and thus ensure it is scientifically sound and gives a clear detailed description of trial related activities.2 To submit protocol and other required study related documents...

Job Opportunity:Clinical Research Associate positions are available for professionals with expertise in conducting research and managing clinical trials. The ideal candidate will have experience in collecting and verifying data from patients, ensuring compliance with protocols and regulatory requirements.A strong understanding of study protocols, informed...

Job Title: Clinical Research Associate\We are seeking a detail-oriented and organized professional to join our team as a Clinical Research Associate. In this role, you will be responsible for conducting clinical trials and studies related to biotechnological and pharmaceutical products.\Key Responsibilities:\Perform routine data collection from patients and...

Job Responsibilities -:• The incumbent will devise a research plan and effective research strategy to conduct market research effectively• Work and design analysis plan and most effective search strategies. Gather required information and filter relevant themes from, subscription databases, the Internet, print media, company representatives, external...