CRC

CRC Morning Star Supportive Services Corporation Glen Ridge, NJ Job Details Full-time $19.00 - $19.50 an hour 1 day ago Qualifications Teamwork Bachelor's degree Attention to detail Health Science Organizational skills Full Job Description Job Overview Join our dynamic team as a Clinical Research Coordinator (CRC), where you will play a vital role in advancing medical research by coordinating and managing clinical trials. You will serve as the essential link between investigators, participants, and regulatory bodies, ensuring that studies are conducted efficiently, ethically, and in compliance with all applicable guidelines. This energetic position offers the opportunity to contribute to groundbreaking healthcare solutions while developing your expertise in clinical research processes. Responsibilities Coordinate all aspects of clinical trial activities, including participant recruitment, screening, enrollment, and follow-up. Ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements throughout the trial lifecycle. Collect, document, and manage study data accurately and securely in accordance with data management standards. Communicate effectively with study participants to provide information, answer questions, and promote retention. Prepare and maintain essential documentation such as case report forms (CRFs), consent forms, and regulatory submissions. Monitor study progress by conducting site visits, audits, and compliance checks to uphold quality standards. Collaborate with investigators, sponsors, and external vendors to facilitate smooth study operations. Qualifications Bachelor's degree in health sciences, nursing, or a related field; advanced degrees are a plus. Prior experience in clinical research or healthcare settings is preferred but not mandatory; relevant internships are welcome. Strong organizational skills with keen attention to detail and accuracy. Excellent communication skills for engaging with diverse stakeholders including participants and regulatory agencies. Knowledge of clinical trial regulations such as FDA guidelines or ICH-GCP standards. Ability to manage multiple tasks efficiently while maintaining a positive attitude. This role offers an exciting opportunity to be at the forefront of medical innovation while working within a collaborative and supportive environment. If you're passionate about making a difference through research and eager to grow your career in clinical trials, we want to hear from you!

Pay:

$19.00 - $19.50 per hour

Work Location:

In person