Clinical Research Coordinator

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

Responsibilities for Clinical Research Associate - Recruit and enroll study participants - Input clinical research data into electronic data systems - Coordinate patient visits and procedures related to research - Act as resource for study participants by answering questions and explaining related procedures - Ensure the study site is compliance with all...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

To monitor clinical trials in various Hospitals. - Coordinate with the Hospital staff for pre - clinical reports. - Ensure proper execution of clinical protocols in the hospitals. - Analyse statistical data generated from the clinical trials. - Prepare report and articles based on the data analysis. - Submit clinical trial documents to the ethics committee...

Clinical Dietitian Mumbai We are looking for a passionate and experienced Clinical Dietitian to join our team at D. S. Research Centre. As a Clinical Dietitian, you will be responsible for creating and implementing individualized nutrition plans for our patients. Responsibilities: Conducting assessments of patients' dietary needs,...

Clinical Dietitian Mumbai We are looking for a passionate and experienced Clinical Dietitian to join our team at D. S. Research Centre. As a Clinical Dietitian, you will be responsible for creating and implementing individualized nutrition plans for our patients. Responsibilities: Conducting assessments of patients' dietary needs, including...

From 10 to 15 year(s) of experience ₹ Not Disclosed by Recruiter - Mumbai (All Areas) - Reviewing all bioequivalence study protocols and reports so as to ensure the quality and to meet regulatory requirements. - Resolving queries raised by regulatory authorities after submission of registration dossier and pre-submission queries raised by our customer -...

**POST: CLINICAL NUTRITIONIST** QUALIFICATION: M.Sc. / PG Diploma in Nutrition Therapy / Dietetics / Clinical Nutrition EXPERIENCE: 1-5 YRS (PREFERABLY HOSPITAL BACKGROUND ONLY) SALARY: Commensurate with Experience **Contact Address**: **INDIAN BURNS RESEARCH SOCIETY** Plot No-1,Sector-13,Airoli-w,Navi Mumbai-400708 Phone No- ...

**Responsiblities**: - Provide clinical study start up expertise. - Assist Lead CRA in the preparation of IRB submissions including the review of the sitespecific informed consent and assent forms - Track IRB submissions - Collect, review, and process essential documents and identify issues that site needs to address. - Communicate to site the updates...

**POST: CLINICAL PSYCHOLOGIST** QUALIFICATION: Master's in **PSYCHOLOGY** EXPERIENCE: 1-5 YRS (PREFERABLY HOSPITAL BACKGROUND ONLY) SALARY: Commensurate with Experience **Contact Address**: **INDIAN BURNS RESEARCH SOCIETY** Plot No-1,Sector-13,Airoli-w,Navi Mumbai-400708 Phone No- 022-27796660 /61/62/63 **NEARBY CANDIDATES PREFERRED.** **Job...

**Essential Job Duties**: - The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study...

**Job Summary**: The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...