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Key Responsibilities: 1. Assist in the design, setup, and monitoring of clinical trials. 2. Communicate effectively with clinical investigators and trial site…
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Job location: Chennai YOUR TASKS AND RESPONSIBILITIES: Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators,…
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Support the setup, initiation, and monitoring of clinical trials. Assist in preparing essential documents, trial master files (TMF), and regulatory submissions. Help…
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Work Schedule Second Shift (Afternoons) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description The Senior Clinical Data…
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Clinical Trial Associate ICON plc is a world leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment…
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Work Schedule Standard (Mon Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description The Senior Clinical Data…
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Work Schedule Standard (Mon Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description The Senior Clinical Data…
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Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full service oncology CRO, and multi…
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Job Description: We are looking for a motivated and detail oriented Research Associate to join our team. The ideal candidate should have…
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Summary Monitors patient data & study related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to…
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Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full service oncology CRO, and multi…
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Clinical Research Coordinator (Freshers Only) Location: [Bangalore or "Across India" if remote/hybrid] Organization: Clinogenesis Research Organization Department: Clinical operations Type: Full Time…
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Work Schedule Standard (Mon Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description The Senior Clinical Data…
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Job Title: Quality Associate- Quality Management System (QMS) Department:Quality Assurance / Quality Management Employment Type: Full time Location: Ameerpet Reports To: Quality…
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At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress,…
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Position: Research Associate, Scientific & Clinical Publications Organization: ARULA for Autism Location: Mumbai Pay Range: Starting INR 35,000/month About ARULA for Autism…
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Kindly Note : FEMALE CANDIDATES FROM CHENNAI ONLY. Please do no apply if you dont fulfill the criteria. Answer screening questions, else…
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Excellent attention to detail, communication, and organizational skills. Strong interest in clinical research and drug development Basic understanding of Good Clinical Practice…
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Key Responsibilities 1. To obtaining Inform Consent Form. 2. To request and maintain accountability of all study related documents. 3. To check…
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Assist in the preparation and coordination of clinical trial protocols and associated documents. Support the monitoring of clinical trials at various stages,…
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