Tuesday, September 10, 2013

Clinical Research Coordinator vacancy at Radiant Research in Kansas City


Radiant Research is currently seeking to employ Clinical Research Coordinator on Fri, 09 Aug 2013 10:02:54 GMT. Radiant Research (radiantresearch.com) is comprised of 20 wholly-owned premier clinical research centers nationwide. Our clinical research centers provides 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…


Clinical Research Coordinator



Location: Kansas City, Kansas


Description: Radiant Research is currently seeking to employ Clinical Research Coordinator right now, this vacancy will be presented in Kansas. Detailed specification about this vacancy opportunity kindly read the description below. Radiant Research (radiantresearch.com) is comprised of 20 wholly-owned premier clinical research centers nationwide. Our clinical research centers provides a critical se! rvice 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, OTC, psychiatry, pulmonary, rheumatology, urology, vaccines and women’s health.


We are currently seeking a full time Clinical Research Coordinator for our Kansas City 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.


Job Responsi! bilities 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 (drawing blood, collecting vital signs, performing ECG’s and processing specimens) 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 and maintains close communication with the sponsor’s Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process. Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols.


A Bachelor’s degree (BA / BS) in a health, sciences or related field and 1+years of recent clinical experience OR an equivalent combination of education and experience is required;


Prior experience with performing ECGs, vitals, etc is required;


Phlebotomy skills are preferred (Certified Medical Assistant, LPN, RN background is helpful);


Prior IATA certification is preferred;


Strong computer skills (use of Microsoft Word, Excel, Outlook) are required;


Exceptional organizational skills, attention to detail and demonstrated human relations and effective communication skills required;


Ability to work well with co-workers, peers, monitors and potential subjects and have a positive attitude;


Ability to effectively and efficiently handle multiple tasks simultaneously with precision and adhere to sponsor requirements;
Ability to ask questions before proceeding to ensure correct an! d accurate results.


Radiant offers a comprehensive benefits package that includes medical, dental, and vision coverage, life and disability insurance, and 401K.


As our company expands there are great opportunities to move up in the organization! To learn more about our company please visit our website at www.radiantresearch.com


Radiant Research is an Equal Opportunity Employer.
– .
If you were eligible to this vacancy, please deliver us your resume, with salary requirements and a resume to Radiant Research.




Interested on this vacancy, just click on the Apply button, you will be redirected to the official website


This vacancy starts available on: Fri, 09 Aug 2013 10:02:54 GMT





Apply Clinical Research Coordinator Here



No comments:

Post a Comment