Clinical Research Coordinator

**Clinical Research Coordinators (Interns / Freshers)** **Pre-Trial Responsibilities**: - Identify and qualify potential clinical trial sites and investigators. - Ensure trial sites are equipped with necessary materials and equipment. - Train site staff on study procedures and data collection methods. - Maintain study manuals and...

**Position - Clinical Research Coordinator** **Qualification - UG - (Any Life Science)** **Timing - General Shift** **Salary - 10K - 14K** **Experience - Fresher - 2 Years** **Language Knows - English/Hindi (Must)** **Joining - Immediately** **Location - Chennai** **Contact No - +91-XXXXXXXXXX **Job Description Clinical Research**: - To have the...

Maintaining the source documents, CRF's, Investigator Site File and other study related documents according to ICH-GCP guideline - Completing the eCRF - Maintenance of Investigational Product according to the specific temperature. Preparing for site qualification visits, initiation visits, monitoring visits and site close out visits. - Organizing ethics...

Job Title: Clinical Research Operations Manager.Job Summary As a clinical research operations manager, you will be responsible for overseeing the day-to-day operations of clinical trials. This includes collaborating with project managers to set targets for clinical monitoring staff, ensuring compliance with project goals. You will also create and implement...

**Protocol Development & compliance** Develop and adhere to comprehensive clinical trial protocols in collaboration with the Principal Investigator **Participant Recruitment and Retention** Implement effective strategies to recruit and retain study participants **Data collection & management** Oversee accurate and timely data collection entry and...

To participate as a research nurse for multiple clinical trials in the hospital and the community Job description 4. Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, data collection, CRF documentation, lab reports filing maintaining source documentation, and EDC query management. 5. Inform...

**Key Responsibilities**: - **Training Program Development**: - Develop and implement a robust training curriculum aligned with industry standards and regulatory requirements. - Create engaging training materials, including presentations, handouts, and online learning modules. - Design and deliver customized training programs to meet the specific needs of...

Job Title: Senior Clinical Research Associate">This is a hybrid position, with two days of work from home and three days in the office. The ideal candidate will have relevant clinical research experience, a degree in health, and advanced knowledge of medical terminology and coding systems.">The role involves providing support to Medical Affairs management...

JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.2.Creating and implementing study-specific clinical monitoring tools and documents.3.Creating and overseeing trial budget.4.Identifying, enlisting and choosing sites, and coordinating site management...

Project ManagerJob Overview:This is a 6-month, full-time role that involves overseeing and coordinating project activities to ensure timely delivery and quality standards. The successful candidate will work closely with overseas physicians to provide updates and guidance on a daily basis.Key Responsibilities:Assist with project planning and...