Clinical Research Coordinator

Coordinate day-to-day activities of clinical trials from initiation to close-out. Recruit, screen, and enroll eligible participants as per study protocol. Schedule and conduct study visits, ensuring adherence to study timelines. Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other...

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...

Job Description A Clinical Research Coordinator is a key member of clinical research teams, responsible for managing and overseeing the day-to-day operations of clinical trials to ensure they run smoothly, ethically, and in compliance with regulatory standards.Key Responsibilities:Recruiting, screening, and enrolling eligible study...

Responsibilities:* Collaborate with cross-functional teams on study start-up, monitoring, and closeout.* Manage clinical trial data from site visits to database lock.Health insuranceAnnual bonus

Job Description:About EquirusEquirus is a leading mid‐market investment bank with strong practices around M&A, PE, Capital Markets, Institutional Equities, Wealth Management, Insurance Broking, and Portfolio Management Services.We pride ourselves in being a trusted Investment bank servicing customer with best results in advisory in their investments, best...

Job Title: AGM / DGM – Clinical Trials (Protocol & Report Writing)Department: Clinical Research / Clinical OperationsMinimum 10–15 yrs of relevant experience in clinical trials, protocol writing, CSR writing, and regulatory documentation

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...