Benefits:
Roth IRA
SIMPLE IRA
Competitive salary
Dental insurance
Health insurance
Paid time off
Training & development
Vision insurance
Location: DuBois, PA Job Type: Full-Time (40hours/wk)
About the Role
Clinical Research Associates of Central PA is seeking a Clinical Research Coordinator (CRC) to support the conduct of industry-sponsored clinical trials. The CRC will assist investigators with the daily management of research studies, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
This role is ideal for someone with clinical research experience or a clinical background. RN or LPN licensure is preferred but not required.
Responsibilities
Coordinate clinical research studies from start-up through close-out
Recruit, screen, and consent study participants
Schedule and conduct study visits according to protocol
Collect and document study data and maintain accurate source documentation
Enter study data into electronic data capture systems
Maintain regulatory files and assist with IRB submissions and updates
Prepare for and support sponsor monitoring visits and audits
Ensure protocol compliance and participant safety
Communicate effectively with investigators, sponsors, and research staff
Qualifications
RN or LPN preferred, but not required
Degree in nursing OR clinical research experience
Knowledge of clinical research processes and regulatory requirements
Strong organizational and documentation skills
Ability to manage multiple studies and deadlines
Experience with electronic data capture systems is a plus
Benefits
Competitive salary based on experience
Opportunity to work with industry-sponsored clinical trials
Professional growth in a collaborative research environment
Exposure to multiple therapeutic areas and clinical studies
Ideal Candidate
The ideal candidate is highly organized, detail-oriented, and comfortable working in a fast-paced clinical environment. This individual enjoys interacting with patients while also managing the regulatory and documentation responsibilities required for clinical research.
Successful candidates will demonstrate:
Strong organizational and time management skills
Ability to manage multiple research protocols simultaneously
Excellent communication skills with patients, investigators, sponsors, and monitors
Attention to detail and commitment to data accuracy and regulatory compliance
Interest in contributing to the advancement of clinical research and new therapies
Clinical experience or research experience is highly valued. RN or LPN candidates are encouraged to apply, though qualified research coordinators without nursing licensure will also be considered.
About Our Company
Clinical Research Associates of Central PA is a growing clinical research site dedicated to supporting the development of new medical treatments through high-quality clinical trials. Our team works closely with physicians, sponsors, and study participants to conduct research in accordance with the highest standards of Good Clinical Practice (GCP) and patient safety.
We participate in industry-sponsored clinical trials across multiple therapeutic areas, providing participants access to innovative therapies while contributing to the advancement of medical science.
Our organization values collaboration, professionalism, and a commitment to excellence in research operations. Team members have the opportunity to gain broad experience across the clinical research process while working in a supportive and mission-driven environment.