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Clinical Research Coordinator

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Job Snapshot
Location:
Mission Viejo, CA 92691 (map it!Map it! )
Employee Type:
Full-Time
Industry:
Healthcare - Health Services
Manages Others:
No
Job Type:
Science
Research
Nurse
Education:
Graduate Degree
Experience:
At least 2 year(s)
Post Date:
11/4/2009
Contact Information
Ref ID:
Clinical Research Coordinator
Fax:
(949)365-0117     instantly fax your resume >>
Description

CLINICAL RESEARCH COORDINATOR

About Us

 

 

Southern California Research is a physician-owned, professionally managed, multi-specialty, multi-site clinical research organization. Our mission is to provide a superior level of service to our sponsors, while pursuing our role as recognized centers of excellence for the Southern California region in phase I-IV multi-specialty clinical trials. SCR is uniquely structured in conducting clinical trials through rapid enrollment, accurate source documentation, highly trained and qualified staff members, and an overall commitment to total quality management of all research protocol activities.

 

Job Description - CLINICAL RESEARCH COORDINATOR

 

Southern California Research seeking full-time Clinical Research Coordinator to provide data management and clinical coordination of research protocols. Clinical applicants must possess a minimum of two years experience working phase 2-4 clinical research drug trials, and completed formal training in GCP, ICH and relevant regulations under CFR.

Clinical ResearchCoordinator  must;

1) Recruit, screen, enroll and obtain informed consent; according to 21CFR50 from clinical trial participants.

2) Coordinate multiple clinical research protocols including arranging necessary patient appointments and ensuring completion of medical procedures by medical staff.

3) Collect, analyze and report clinical trial data to phara sponsors with specified timelines.

4)  Assist in the preparation and submission of IRB/regulatory documents and ensure compliance with relevant IRB and other regulatory requirements (including 21CFR312);

5)  Collaborate on the development of clinical trial materials including educational materials, marketing materials, reports, etc.

6) Maintain project timelines including tracking deadlines for clinical data collections, record keeping, and transmission of of verbal and written communication to pharmaceutical companies.

7) Maintain accurate and current study and regulatory binders/manuals

Requirements

 

Applicants must possess;

  • A minimum of two years experience working phase 2-4 clinical research drug trials,

  • Applicants must have completed formal training in GCP, ICH and relevant regulations under CFR.

  • RN’s or LVN’s encouraged to apply

  • Must be willing to work (4) day 10 hour work week

 

***We offer a competitive salary and benefits package including a 401K***

Come Join A Winning Team!

 

  • Location: MISSION VIEJO, CA

  • Compensation: negotiable

  • Principals only. Recruiters, please don't contact this job poster.

  • Please, no phone calls about this job!

  • Please do not contact job poster about other services, products or commercial interests.

To submit resume, please click "APPLY NOW"

 

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