Clinical Trial Coordinator

Support and coordinate day-to-day clinical trial activities - Work with research participants about the trial and participation rules - Oversee medication administration or device usage - Conduct data collection and record reported results, as well as volunteer information - Provide guidance on compliance with various guidelines and communicate any...

**Responsibilities**: - Maintain and organize Trial Master File (TMF) and essential documents. - Track study progress, including patient enrollment and site communications. - Assist with the preparation and submission of regulatory documents. - Schedule meetings, take minutes, and support trial team coordination. - Ensure compliance with Good Clinical...

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Company DescriptionVivoclin Research Services specializes in conducting clinical trials, with a focus on rheumatology, dermatology, and oncology. The company is dedicated to advancing medical research and providing innovative solutions in the healthcare industry. Vivoclin Research Services bridges the gap between clinical trials and breakthrough treatments,...

Company DescriptionSapientia Medicus Research is a global leader in Site Management Organization (SMO) services with presence in India and Canada, specializing in supporting clinical research in various therapeutic areas such as oncology, ophthalmology, nephrology, and more. Known for its expertise in rapid patient enrollment and accurate data collection,...

Job Responsibility: ❖ Lead and manage the day-to-day conduct of clinical trials at the site. ❖ Ensure adherence to study protocols, ICH-GCP guidelines, and regulatory requirements. ❖ Serve as the primary point of contact between the site and the sponsor/CRO. ❖ Prepare, submit, and maintain regulatory documents (e.g., EC/IRB submissions, clinical...

Assist in the coordination and conduct of clinical trials under supervision - Support patient recruitment, screening, and enrollment according to protocol criteria - Schedule and manage patient visits, sample collection, and follow-ups - Collect and accurately enter data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems - Maintain...

Clinical Research Coordinator Responsibilities and DutiesCoordinate and manage clinical trial activities from initiation to close-outRecruit, screen, and enroll study participants according to protocol criteriaObtain informed consent and ensure participant understandingSchedule and conduct study visits, procedures, and assessmentsMaintain accurate and...

Role & responsibilitiesEC Submission• To get the documents from Central Drive, print, prepare files accordingly, and dispatch them to the respective sites prior to the Ethics Committee meeting conducted at site.SIV (Site Initiation Visit) Kits Preparation• To co-ordinate with CRD and prepare the SIV kits, study related material (NS Bottle, Syringe &...

Job Title: Clinical Research Associate (CRA) - Location: Gota, Ahmedabad - Positions Available: 2 - Experience Required: 4 to 12 Years - Salary Range: Up to ₹8 LPA (Based on experience and skills) **Roles & Responsibilities**: - Perform the duty of Clinical research associate - Perform on-site in-process and retrospective monitoring visit of clinical...