Clinical Research Coordinator

Kickstart your career inClinical Researchwith us We atS3 Clinical Researchare looking for02 passionate internsinAhmedabadfor aGlobal Clinical Trialproject. What's in it for you? 6-month (180 days) structured internship Internship Certificate to boost your profile Incentive for top performers Best performers will behired as CRCat S3 Clinical ResearchThis is...

Hello Science Graduates!! , We have a Brilliant Career Opportunities for you into " Clinical Research with Pharma, Biotech, Healthcare R & D sectors to PAN INDIA " So if you are interested for global & respectable ,good salary based research career then kindly revert me with your latest updated CV with contact number to discuss it further. Thanks for all...

Job Description for Clinical Research Associate 1. Identify and qualify potential investigators to ensure that the sites have adequate time and can fulfill their obligation to the study. 2. To review research protocols and amendments, informed consent documents, case report form and/or other applicable business and project related documents to provide the...

**Job Summary**: We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to manage and coordinate clinical trials, ensuring compliance with regulatory guidelines and protocols. The CRC will work closely with principal investigators, study participants, and regulatory bodies to support successful trial execution. **Key...

**Responsibilities** - Develop and maintain study protocols and case report forms. - Recruit and screen study participants per study criteria. - Obtain informed consent from study participants and explain study procedures. - Collect and manage study data, including adverse events and other safety-related information. - Monitor study participant compliance...

Coordinate day-to-day activities of clinical trials from initiation to close-out. Recruit, screen, and enroll eligible participants as per study protocol. Schedule and conduct study visits, ensuring adherence to study timelines. Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other...

Coordinate day-to-day activities of clinical trials from initiation to close-out. Recruit, screen, and enroll eligible participants as per study protocol. Schedule and conduct study visits, ensuring adherence to study timelines. Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other...

Help us bring cutting-edge medical treatments to life Become a key player in clinical research and accelerate advancements in healthcare.OpportunitiesWe offer two paths into the exciting world of clinical research:Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager...

Overseeing the smooth running of clinical trials. - Collecting, coding, and analyzing data obtained from research. - Managing research budgets. - Informing participants about study objectives. - Administering questionnaires. - Monitoring research participants to ensure adherence to study rules. - Adhering to research regulatory standards. - Adhering to...

Overseeing the trouble-free running of clinical trials Collecting data obtained from research, coding and analyzing it Managing budgets set aside for research Communicating with participants regarding study objectives Administering questionnaires and monitoring participants to ensure they adhere to the studys rules Liaising with laboratories regarding...