Clinical Research Coordinator

posted:
Location
Tulsa, Oklahoma
Industry
Administrative & Support Services (Office and Administrative Support Occupations)
Job Type
Temporary
Working Hours
8:00 AM - 5:00 PM
Salary
US$ 28.00 - US$ 38.00 per hour
Ref. Number
S_40395
Contact
Whitaker,Barbe, Spherion
Phone
918-9715900
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Job Description

Our client is a global leader who has experienced and dedicated experts who work together to deliver conventional and innovative treatments for patients. They are seeking candidates to fill the Clinical Research Coordinator positions that will perform phases of oncology research studies and maintain and assure protocol compliance for all research subjects.
The Clinical Research Coordinator will have in-depth knowledge of applicable federal regulations, institutional guidance documents and SOP's relating to clinical trials to ensure human subject protection, compliance with protocol and the recording and maintenance of data and source documentation.
This position is considered a six-nine month contract and the pay is $59k-$78.5k, based on experience.
If this sounds like a perfect fit for you, apply today! If you would like additional information, please call our office. 918/971-5900

Responsibilities:
-Collaborate with physicians in review of probable protocols
-Organize study data for reports, analyses and for conference presentations and publications
-Recruit and screen prospective subjects to determine eligibility
-Monitor subjects for adverse events through analysis of clinical reports, laboratory and imaging results and subject interviews
-Perform timely and accurate IRB reporting which includes protocol, ICF, amendments, IND safety reports, etc.

Working hours: 8:00 AM - 5:00 PM

Skills:
-Direct subject contact and knowledge of clinical tasks associated with research such as phlebotomy, centrifugation, specimen processing and subject interviews
-Current working knowledge of FDA, OHRP, HIPPA, ICH and GCP regulations and guidelines
-Responsible for clinical trials management including subject screening, interviewing, basic procedures, data collection, CRF's and computerized data management systems
-Strong written and verbal communication and customer service skills
-Attention to detail and organizational skills

Education:
Bachelors

Experience:
4-7 years

Qualifications:
-Bachelor's degree in a healthcare or business related field with healthcare experience (Business Administration, Health Care Administration or clinical science, health, medicine, pharmacy or nursing field) required, Master?s degree preferred
-Certification through SoCRA, ACRP or other reputable entity within 3 years
-Human Subjects Protection training/certification within 90 days
-Basic Oncology class within 1 year of employment
-3+ years of research and clinical oncology experience preferred
-Phase I clinical research experience preferred
-Computer literacy with knowledge of word processing, spreadsheet, presentation and database software (Word, Excel, Access and Power Pont) required


If this sounds like a perfect fit for you, apply today! If you would like additional information, please call our office. 918/971-5900

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

Apply Now