Clinical Research Associate

Job Description of Clinical Data Associate.To co-ordinate with the respective Study Lead of the CDM department to ensure effective study progress and support the Study Lead in departmental functions and activities at Cliantha Research.A. Create, maintain and update study specific documents like Data Management Plan, Creation of Data Validation Plan, database...

ORGANISATIONAL OVERVIEWLambda Therapeutic Research is a full- service Global Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland) and London (UK), Lambda offer comprehensive end-to end...

Job Description for Sr Research AssociateJob Description:We are looking for skilled Sr Research Associate with 3–5 years of experience in the clinical research domain, specializing in Extractables & Leachable (E&L) and Elemental analytical studies. The role involves supporting method development, method validation, and sample analysis while ensuring full...

Company :Manufacturer, exporter, distributor, and supplier oforthopedic and arthroscopic medical devices. Their products include a wide range of orthopedic implants, surgical instruments, arthroscopy equipment, reconstruction nails, and joint replacement components.Position :Manager - Clinical ResearchDepartment :Regulatory AffairsJob SummaryThe Manager –...

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...

Clinical Research Coordinators provide support & coordination for drug/device studies that may involve industry-sponsored Phase I, II, III, and IV clinical trials,Ensure smooth, accurate progress of clinical studies from the planning and approval stages through study completion and post-study closureThe role involves using an in-depth knowledge of trial...

The Manager Clinical Research is responsible for planning, designing, and managing clinical investigations for medical devices in accordance with CDSCO, EU MDR, ISO 14155, ICH-GCP, and NDCT-2019 requirements. The role ensures generation of high-quality clinical evidence to support product safety, performance, regulatory approvals, and post-market...

DepartmentZTIJob posted onJan 08, 2026Employment typeP-P5-Probationer-R&D StaffRESPONSIBILITIES:Manage assigned investigational sites in a remote capacity.Perform remote monitoring of assigned investigational sites, including: site qualification visits, site initiation visits, routine monitoring visits, and close-out visits.Support Project Management in the...

Medical OversightProvide ongoing medical monitoring of assigned clinical trials, including real-time safety review of adverse events (AEs) and serious adverse events (SAEs).Evaluate safety signals, trends, and laboratory/ECG abnormalities to ensure participant well-being.Assess investigator-reported causality and provide independent medical judgment when...

We Are Hiring: Senior Research Associate – Regulatory AffairsAre you a seasoned Regulatory Affairs professional with a passion for global impact?We're looking for aSenior Research Associate – Regulatory Affairswith strong expertise inEuropean, Asian, and EU regulatory marketsto join our team.Key Requirements: Hands-on experience withEU & Asian regulatory...