Clinical Research Coordinator

Position - Clinical Research CoordinatorExperience - Must 1 Years (Experience in Clinical Research)Timing - General ShiftQualification – Bio ScienceSalary – K (based on your experience it may differ)Contract Period - Minimum 2 Years (No Bond)Location - AhmedabadLanguage Knows – Gujarati/English/TamilContact Number JOB Description Clinical Research...

**Clinical Research Associate II - Clinical Trial** Department Clinical Trials Designation Clinical Research Associate II Basic qualification B. Pharm / M. Pharm / M. Sc. required Experience 2 - 4 Years - Site monitoring Location Ahmedabad Brief JD 1. Identify and qualify potential investigators to ensure that the sites have adequate time and can...

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...

We are seeking a motivated and detail-oriented Entry-Level Clinical Research Associate to join our team.This role is ideal for recent graduates or freshers with a background in life sciences or pharmacy, looking to build a career in clinical research

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...

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...

Role & responsibilitiesResponsible for clinical trial medical science related activities like preparation of protocol, Informed consent form, CRF, other study related documents and SOPs in line with ICH GCP, Indian and global regulatory.Conduct relevant literature search for required for protocol and manuscript writing.Ensures that medical writing...

Coordinate and manage clinical trials, ensure compliance with protocols and GCP, handle participant recruitment and documentation, liaise with investigators and sponsors, maintain accurate study data, support site monitoring & regulatory activities.

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...

Role & responsibilitiesDevelop and manage comprehensive project plans, including timelines, budgets, resource allocation, and risk mitigation strategies.Oversee all aspects of trial startup, including site selection, contract negotiation, IEC/IRB submissions, and study team training.Monitor trial progress against established milestones and timelines,...