Clinical Trial Administrator

Customer Engagement as SME continuous support in both pre-sales and post-sales phases Provide deep subject matter expertise on Clinical Trial processes and related systems. Support BD team with system demonstrations, domain insights, Required Candidate profileExperience in Clinical Trials, EDC, CDM, Clinical systems Trails Solutions. Understanding of...

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 &...

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,...

BioDev is looking for experienced Clinical Team Leads for its growing portfolio of international clinical trials & pharma R&D projects. Only candidates with experience of at least 2 years in Phase 1/2/3 clinical trials and Site Monitoring will be considered. These will be office based, travelling roles - locations Ahmedabad. An understanding of allied...

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,...

DivisionCROJob posted onNov 26, 2025Employee TypeC-C6-Confirmed-R&D ExecutiveExperience range (Years)10 years - 20 yearsRole PurposeResponsible for Management of Clinical Trial.Areas (% of time)Key Accountabilities/ ResponsibilitiesProject Management (45%)Identify, prepare and optimize project resources and schedule.Review of Protocol, ICF, Clinical study...

Clinical Research Associate (CRA) / Clinical Research Coordinator (CRC)Location:USAEmployment Type:Full-time Job SummaryWe are looking for a detail-oriented and motivated Clinical Research professional to support clinical trials, ensure protocol compliance, manage documentation, and coordinate with investigators, sponsors, and participants. Key...

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...

Responsibilities:* Lead clinical trials from start to finish* Manage site selection, initiation & monitoring* Ensure compliance with ICH-GCP guidelines* Design protocols & review applicationsProvident fundOffice cab/shuttleHealth insuranceAnnual bonus

Role & responsibilitiesConduct external site audit (Late Phase) to ensure compliance with SOPs, Protocol, ICH GCP, and applicable regulatory requirements.Review of study documents like study protocol, inform consent, eCRF, Data management plan, study plans, Statistical analysis plan (SAP), clinical study report, etc.Audit study database in various clinical...