Clinical Research Associate

Eligibility: - Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute - Prior knowledge of the conduct of Clinical Trials, - Phases of Clinical trials and - Thorough Knowledge of ICH-GCP and other regulatory guidelines. Roles and Responsibilities: - Prepare the Database of the Investigators at the place assigned to you. - Interact...

**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...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:- Conduct site visits to monitor trial activities and ensure compliance...

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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...

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

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...

**Title**: Clinical Programmer **Department**: Engineering Support the organization’s mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, innovation, respect, commitment to our community, and accountability and ownership. Job SummaryPrimary responsibilities are clinical programming and data...

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...

ResponsibilitiesSupport 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...

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...

Name of the post :Research Associate (1 Post)Project :NFSM (In – Vivo Health Benefits)Emoluments :Rs. 49,000/- per month + HRA for master degree holders &Rs. 54,000/- per month + HRA for Ph.D holders (HRA as per ICAR rules)Project till :April, 2025Essential Qualifications:With Doctoral Degree:Ph.D. in Food Sciences & Nutrition/ Food Chemistry/ Food...

Name of the post : Research Associate (1 Post) Project : NFSM (In – Vivo Health Benefits) Emoluments : Rs. 49,000/- per month + HRA for master degree holders & Rs. 54,000/- per month + HRA for Ph.D holders (HRA as per ICAR rules) Project till : April, 2025Essential Qualifications:With Doctoral Degree:Ph.D. in Food Sciences & Nutrition/ Food...

Name of the post : Research Associate (1 Post) Project : NFSM (In – Vivo Health Benefits) Emoluments : Rs. 49,000/- per month + HRA for master degree holders & Rs. 54,000/- per month + HRA for Ph.D holders (HRA as per ICAR rules) Project till : April, 2025Essential Qualifications:With Doctoral Degree:Ph.D. in Food Sciences & Nutrition/ Food...

As an Associate/Content Editor in Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyze, cross reference, and update all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences, trial registries, press releases and other possible...

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...

Associate Clinical Data Manager SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great...

Your responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...

Collecting data obtained from research, coding and analyzing it Managing budgets set aside for research Communicating with participants regarding study objectives Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules Liaising with laboratories regarding research findings Monitoring the study to ensure that...