Clinical Research Associate

Eligibility: - Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute - Prior knowledge of the conduct of Clinical Trials, - Phases of Clinical trials and - Thorough Knowledge of ICH-GCP and other regulatory guidelines. Roles and Responsibilities: - Prepare the Database of the Investigators at the place assigned to you. - Interact...

(On Site)Call/WhatsApp: Ms. Chahat)Salary: SGD 10,000 per month (Minimum)We are looking for Clinical Researchers who want to live and work in Singapore.**SERVICE CHARGES APPLICABLECompany DescriptionVinfinity Immigration is a leading and trusted consultancy with over a thousand satisfied clients worldwide and an impeccable success rate over the last 9 years....

Clinical Research Training, Clinical Research Assessments, Clinical Research Mock Tests, Clinical Research Overview, Clinical Research Mock Interviews, Clinical Trial Management **Job Types**: Full-time, Part-time, Contractual / Temporary, Freelance Expected hours: No less than 40 per week Schedule: - Day shift **Experience**: - total work: 5...

The Clinical Research Associate will oversee clinical trial activities to ensure ethical conduct, regulatory compliance, and high-quality data generation.Roles & Responsibilities:Assist in planning, initiation, execution, and closure of clinical trials.Conduct site monitoring visits (site selection, initiation, monitoring, close-out).Ensure adherence to...

**Company Description** IACR RESEARCH INSTITUTE stands out in India by providing live, engaging, and interactive sessions to students, allowing them to clear their doubts with expert trainers. Understanding that many freshers face challenges such as stage fear and communication issues, IACRI offers soft-skills training and personal development. Regular...

Designation : Clinical Research CoordinatorFacilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.Working closely with the PI ,CRC participates in an integral way in the informed consent process by communicating with the potential study subjects about protocol. Possesses a thorough knowledge of...

Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies. Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identifies protocol problems, informs investigators of problems, or assists in problem...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

Clinical Research Training Develop and deliver a course on clinical trials, covering topics like study design, patient recruitment, data collection, and regulatory compliance. They would then assess student progress through quizzes and case studies, providing feedback to help them improve their understanding and skills. Additionally, they might offer...

Research Associate **Role and Responsibilities**: - ** Comprehensive Research**: Perform detailed secondary research to create comprehensive profiles of Food, Nutritional, Pharmaceutical products, including drugs, clinical studies, and medical devices. - ** Data Capture**: Collect and analyze data from a variety of sources such as press releases, annual...