Clinical Research Coordinator (local recruits only)

Position:

Clinical Research Coordinator Experience:

Minimum 2 years in conducting Phase II-IV pharmaceutical clinical trials Are you an experienced Clinical Research Coordinator looking for an exciting opportunity to contribute to cutting-edge medical research? We are a rapidly expanding clinical trials center specializing in Phase II-IV studies across multiple medical specialties, and we are seeking a motivated and detail-oriented CRC to join our team. Key Responsibilities As a Clinical Research Coordinator, you will play a pivotal role in the successful execution of our research studies.

Your primary responsibilities will include:

Key Responsibilities Collaborate closely with Principal Investigators to coordinate all aspects of assigned clinical studies, including participant recruitment, eligibility assessment, scheduling, treatment coordination, and study-related procedures. Perform clinical and study-related procedures, including phlebotomy, vital signs collection, centrifuge operation, ECG administration, and other protocol-required tasks. Utilize Microsoft Office and electronic research systems efficiently, including source documentation platforms, IXRS/IWRS, and Electronic Data Capture (EDC) systems such as Medidata, Veeva, and Inform. Monitor participant health status throughout the study and promptly communicate relevant findings to the Principal Investigator. Identify, document, and report Serious Adverse Events (SAEs) and other safety concerns to investigators and sponsors in accordance with protocol and regulatory requirements. Coordinate the collection, processing, packaging, and shipment of biological specimens to designated central laboratories, ensuring accuracy and compliance with laboratory and shipping guidelines. Maintain accurate, complete, and organized study documentation in compliance with GCP and regulatory standards. Qualifications Minimum of 2 years of hands-on experience as a Clinical Research Coordinator, preferably in Phase II-IV pharmaceutical clinical trials. Bachelor's degree in a scientific, healthcare, or related field. Strong attention to detail with the ability to maintain accurate and well-organized research records. Excellent written and verbal communication skills, with the ability to interact professionally with investigators, sponsors, participants, and study team members. Working knowledge of ethical principles, regulatory requirements, and GCP guidelines governing clinical research. Ability to recognize potential risks, protocol deviations, and adverse events and respond promptly and appropriately. Join a collaborative, fast-paced research environment where your expertise will directly contribute to advancing medical treatments and improving patient care. If you meet the qualifications and are ready to make a meaningful impact, we encourage you to apply.

To Apply:

Please submit your resume along with a cover letter outlining your relevant experience and interest in the position. We look forward to connecting with qualified candidates.

Job Type:

Full-time Benefits:

401(k) matching Dental insurance Health insurance Paid time off Vision insurance

Work Location:

In person