Clinical Research Coordinator

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...

Ø Clinical Research - Pre-clinical/Clinical studies Ø Technical content writing Ø Literature Reviews Ø Writing research papers/white paper Ø Market Research Analysis Ø Statistics Ø Technical Dossier Ø To coordinate with R&D, QA, QC & Technical Services Departments. Pay: ₹500,000.00 - ₹600,000.00 per year **Benefits**: - Provident...

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 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 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...

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. \

Liable for advising **team (Internal & External) both on Non clinical and clinical exercises **with respect to ODS Aligners. - Go about as a vital part to share future proposals to ODS Aligners. - As a piece of a clinical coordinator team, you will be **liable for** **Patient's Intra-Oral Scan.** - **Addressing patients concern** and resolving personally on...

Job Title: Clinical Research Associate\We are seeking a detail-oriented and organized professional to join our team as a Clinical Research Associate. In this role, you will be responsible for conducting clinical trials and studies related to biotechnological and pharmaceutical products.\Key Responsibilities:\Perform routine data collection from patients and...

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...