Clinical Trial Administrator

The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization.Role & responsibilitiesIs...

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 &...

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...

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...

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...

Assist in the setup, testing, and maintenance of clinical databases (EDC systems).Perform data entry, data validation, and discrepancy management.Review Case Report Forms (CRFs) and ensure accuracy, completeness, and consistency of clinical trial data.Support data cleaning activities, query generation, and resolution with study teams.Maintain study...

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...

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

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...

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...