Clinical Research associate-Reputed Medical

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics committee...

JOB DETAILS 1 Performing routine data collection from patients,2 Verifying data sources, and reviewing regulatory documents/files to ensure that documents are in compliance with protocols, regulatory requirement3 SOPs (standard operating procedures), and are aligned with the Monitoring Plan.4 Some clinical research associates assist in reviewing study...

Job Title: Clinical Research Associate (CRA) - Ayurveda Job Summary: Key Responsibilities: 1. Clinical Trial Management: Manage clinical trials from initiation to close-out, ensuring compliance with GCP, regulatory requirements, and company SOPs. 2. Site Management: Coordinate with research sites, investigators, and site staff to ensure timely trial...

Job Title: Clinical Research Associate">To ensure the successful planning, execution, and monitoring of clinical trials, we are seeking a highly skilled Clinical Research Scientist. \

**Responsibilities for Clinical Research Coordinator** - Responsible for ensuring study is compliance with local and federal laws and regulations - Recruits and screens potential study participants and performs intake assessments - Creates and/or maintains all documents and records related to the study - Acts as a point of reference for study participants by...

About the Role\ As a Clinical Research Associate, you will be responsible for conducting clinical trials and ensuring compliance with regulatory requirements. Your duties will include creating and writing trial protocols, identifying and establishing trial sites, training site staff, liaising with ethics committees, managing IP and trial materials, and...

JOB DETAILS 1 To provide timely inputs in the protocol and Informed Consent (for e.g. dosing information, contraindications, warnings, precautions, adverse events, and drug interactions) and thus ensure it is scientifically sound and gives a clear detailed description of trial related activities.2 To submit protocol and other required study related documents...

Company DescriptionSkylimit Research Private Limited provides a comprehensive range of clinical, preclinical, and bio/analytical services supporting innovator, biosimilar, and generic drug development programs globally. As an independent, investor-owned, and professionally managed contract research group, we offer scientific leadership, robust quality...

Job Opportunity Clinical Research Associate Role: A Detailed OverviewThis role involves collaborating with the steering committee to create and present trial protocols. Identifying, evaluating, and establishing trial sites is a crucial aspect of this position. Additionally, training site staff on therapeutic areas, protocol requirements, and proper...

JOB DETAILS 1.Be the medical expert for the therapy area and the medical lead within the brand teaminputting into the strategy for the brand2.Support the Medical Director in carrying out the day to day operational activities of theMedical Department.3.Review and sign-off of promotional and non-promotinal material to ensure compliancewith the Codes of...