Clinical Research Coordinator

Clinical Research Coordinator

Posted by Top Rated Company in Medical Services Sector

Hyderabad,Chennai,Bengaluru

Posted: imported by Jeevika

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A clinical research associate, also known as a CRA, conducts research to ensure these products are safe.Responsibilities: 1. Assist in Protocol Development: Collaborate with the clinical research team to contribute to the development and review of clinical trial protocols.2. Site Identification and Selection: Participate in the process of identifying and selecting clinical trial sites by conducting feasibility assessments. 3. Regulatory Compliance: Support the team in ensuring regulatory compliance throughout the clinical trial process. Assist in the preparation and submission of regulatory documents to appropriate health authorities. 4. Site Initiation: Assist in the initiation of clinical trial sites by coordinating site training activities and ensuring that all necessary documentation is in place. 5. Monitoring and Data Collection: Work closely with clinical research associates and investigators to monitor and collect data during the clinical trial. Assist in ensuring data accuracy, completeness, and adherence to protocol. 6. Adverse Event Reporting: Contribute to the process of monitoring and reporting adverse events, ensuring compliance with regulatory requirements. 7. Study Close-Out: Participate in the close-out activities of clinical trials, including the collection of essential documents and finalizing study reports. 8. Collaboration and Communication: Work collaboratively with cross-functional teams, including clinical operations, data management, and regulatory affairs. Communicate effectively with investigators, site staff, and study sponsors. 9. Documentation and Record Keeping: Maintain accurate and up-to-date documentation of all activities performed during the internship. Contribute to the development and organization of the trial master file. 10. Learning and Development: Actively engage in learning opportunities provided during the internship to enhance knowledge of clinical research processes and industry regulations. Qualifications: Currently enrolled in a bachelor's or master's degree program in a related field (e.g., life sciences, pharmacy, nursing, etc.). Excellent communication and interpersonal skills. Detail-oriented with strong organizational and time management abilities. Ability to work independently and as part of a team. Role & responsibilities.Preferred candidate profile Role: Clinical Informatics,Industry Type: IT Services & Consulting,Department: Healthcare & Life Sciences,Employment Type: Full Time, PermanentRole Category: Health InformaticsEducationUG: B.Sc in Bio-Chemistry, Bioinformatics, Clinical Pathology, Biology, Microbiology, Botany, Chemistry, Medical, Biotechnology, Botany Zoology and Chemistry, B.Pharma in Clinical Pharmacy, Pharmacology, M.B.B.S. in Medicine, PathologyKey SkillsSkills highlighted with ‘‘ are preferred keyskillsClinical OperationsClinical ResearchClinical Data ManagementClinical DatabaseClinicalBiochemistryClinical DevelopmentPharmacovigilanceClinical TrialsClinical PharmacyClinical MonitoringPharmacyDrug SafetyClinical DocumentationClinical DataAbout company 39/4, 2nd Cross, 1st Main Rooppena, Agrahara, B. Halli, Bommanahalli (Bangalore), Bangalore South, , BANGALORE, Karnataka, IndiaCompany InfoAddress: 39/4, 2nd Cross, 1st Main Rooppena, Agrahara, B. Halli, Bommanahalli (Bangalore), Bangalore South , , BANGALORE, Karnataka, IndiaBeware of imposters! Naukri.com does not promise a job or an interview in exchange of money. 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