Radiant Research (radiantresearch.com) is comprised of 25 wholly-owned premier clinical research centers nationwide. Our clinical research centers provide a critical service to biopharmaceutical companies by recruiting study participants into clinical research, conducting the clinical research protocol and collecting the data necessary to support the safety and efficacy of the drug company's product to the FDA. Our client list includes every major pharmaceutical company and contract research organization and many biotechnology and medical device companies. Radiant's areas of study include: asthma/allergy, cardiology, dermatology, endocrinology, gastroenterology, general medicine, infectious disease, men's health, musculoskeletal, neurology, nutrition, over OTC, psychiatry, pulmonary, rheumatology, urology, vaccines and women's health. We are seeking a part time Clinical Research Coordinator, with the possibility of moving to full time in the future, for our Overland Park, KS site. Working under the supervision of the Principal Investigator and Site Director, this position will coordinate the conduct of clinical drug studies from pre-study planning through successful completion of all patient visits and documentation. The Coordinator is directly involved in patient care. Job Responsibilities include: • Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. • Responsible for completion of all study documentation forms, including case report forms and other study specific documents. • Coordinate and conduct patient care visits and assure all procedures are conducted in compliance with the clinical protocol. • Interact with Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed, alerts Principal Investigator of serious adverse events. • Interacts with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process. • Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols • Conducts clinical research in compliance with all applicable regulations. Qualifications: • BA/BS with 2+ years CRC experience (Certified Medical Assistant helpful) • RN or LPN preferred • ACRP coordinator certification or SoCRA clinical research professional certification as well as active CPR certification a plus • At least two years of recent clinical experience strongly preferred • Phlebotomy skills, strongly preferred • Ability to work well with co-workers, peers, monitors and potential subjects. • Ability to effectively and efficiently handle multiple tasks simultaneously with precision and adhere to sponsor requirements • The candidate should be able to promote a teamwork philosophy with a positive attitude. We offer a competitive benefits package with medical, dental, and vision coverage, life and disability insurance, and 401K. Radiant Research is an Equal Opportunity Employer.