Clinical Research Coordinator

Kickstart your career inClinical Researchwith us We atS3 Clinical Researchare looking for02 passionate internsinAhmedabadfor aGlobal Clinical Trialproject. What's in it for you? 6-month (180 days) structured internship Internship Certificate to boost your profile Incentive for top performers Best performers will behired as CRCat S3 Clinical ResearchThis is...

Company DescriptionHREE Research Pvt. Ltd. is a full-service Clinical Research Organization (CRO) offering comprehensive, end-to-end clinical research solutions. We specialize in supporting pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials. Our services include study design and protocol development, regulatory...

S3 Clinical Research is expanding, and we are looking for adedicated Phlebotomistto join our team. Position:Phlebotomist Organization:S3 Clinical Research - Clinical Lab Vertical Location:Ahmedabad Joining:ImmediateKey Responsibilities:Collecting and handling blood samples with precision and care.Maintaining proper labeling, documentation, and storage of...

About the Role:Key role as a project manager would be Single Point of Contact (SPOC) for the Sponsor from Sterling Accuris Wellness Pvt. Ltd. for laboratory testing and the associate services for clinical trials.The role will require the ability to support the clinical trial study pipeline which could include various projects covering various therapeutic...

Assist in the coordination and conduct of clinical trials under supervisionSupport patient recruitment, screening, and enrollment according to protocol criteriaSchedule and manage patient visits, sample collection, and follow-upsCollect and accurately enter data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systemsMaintain essential...

*QC Reviewer (Clinic):*1) Review of clinical raw data as per predefined Quality Control Plan for completeness, accuracy, and for compliance with the Study Protocol, GCP, SOPs and applicable regulatory Guidelines.2) Online Monitoring of study activities to ensure that studies are conducted in accordance with GCP, SOPs, Protocol and applicable regulatory...

ResponsibilitiesOversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities.Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study...

Dear Candidate,Below are the Job Details for Clinical SAS Programmer role at CBCC Global Research LLP.Candidate should have the exposure of SDTM, ADAM and TLF.Job Location : Ahmedabad At OfficePosition : 2Experience: 2-5 years in CRO preferred / Pharma industryQualification : M. Sc. Statistics/Any Science GraduateMandatory experience in Clinical...

MBBS with MD; JD preferred. Proven experience in hospital clinical operations and leadership required.Strong coordination skills with clinical departments and a focus on quality patient care

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of...