Job Vacant for Clinical Research Coordinator

Position - Clinical Research Coordinator Experience - Above 1 Years Timing - General Shift Qualification - B.Sc Nursing/DGNM (Nurse Only Eligible) Salary - 15K - 18K ( per month) Contract Period - Minimum 2 Years(Not Bond) Location - Chennai Contact Number - 044-28295465 JOB Description Clinical Research Coordinator - To have the good knowledge of...

**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...

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...

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...

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 description** - Manage Clinical & Non-Clinical study portfolios - design & develop protocols along with other clinical trial documents & reports that fit with the regulatory pathway and standards - Responsible for planning, scheduling and implementing the clinical aspects of projects in-line with Monitoring Plan, Recruitment Plan, Clinical Training...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians)3.setting up and disbanding trial study centres4.designing trial materials and supplying study centres with sufficient quantities5.providing clinicians with instructions on how to conduct the trials6.collecting and authenticating...