University of Utah Clinical Site Monitor in Salt Lake City, Utah
Open Date 04/09/2018
Requisition Number PRN16858B
Job Title Clinical Site Monitor
Working Title Clinical Site Monitor
Job Grade F
FLSA Code Administrative
Patient Sensitive Job Code? Yes
Standard Hours per Week 40
Full Time or Part Time? Full Time
Work Schedule Summary
VP Area President
Department 01345 - HCI Clinical Resrch Compliance
City Salt Lake City, UT
Type of Recruitment External Posting
Pay Rate Range 47600 to 69000
Open Until Filled Yes
Conduct monitoring of investigator-initiated oncology clinical trials to ensure compliance to the protocol, regulations, guidance and standard operating procedures. Recommend corrections to monitoring findings and enhancements to study protocols and to operating policies and procedures. Report study progress, toxicity summary and compliance issues to theHCIData and Safety Monitoring Committee (DSMC). Coordinate and oversee participation of outside sites on Huntsman Cancer Institute multi-site clinical trials.
1.Oversee, coordinate and conduct quality assurance reviews, including monitor and audit visits on cancer related clinical trials to ensure compliance with study protocol, University, state and federal guidelines.
2.Compile comprehensive reports for Principal Investigators,DSMCand other committees as assigned.
3.Administer and Support the Data and Safety Monitoring Committee.
4.Assist in protocol development and maintenance.
5.Develop, monitor, and update study specific case report forms and progress of the electronic data capture for each study.
6.Analyze and document compliance processes. Recommends enhancements to operating policies and procedures for compliance review. Develop departmental SOPs.
7.Develop, coordinate and participate in educational and training programs to enhance compliance and awareness of compliance issues.
8.Maintain current knowledge regarding federal and state guidance, including Good Clinical Practice (GCP).
Incumbent is responsible for assisting the University in preparation for regulatory audits by developing, monitoring and updating quality controls and recommending actions to maintain compliance. This position is the primary contact and expert regarding regulatory agency standards governing clinical trials. Representative challenges of this position include determining the validity of collected data, assessing process shortfalls, and developing effective safeguards to reduce risk. The incumbent must possess the ability to foster collaborative working relationships with a wide range of constituencies.
This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
Bachelor’s degree in a health science or related field or equivalency; and four years of clinical research experience that includes regulatory compliance monitoring/auditing,IRBapplication submission, and experience in human subjects research. Must have a working knowledge ofFDA,ICH, and other regulatory compliance; an understanding of medical terminology and technical writing experience. Excellent interpersonal communication (including oral and written) and leadership skills also required. Must be proficient in Microsoft Office and possess the ability to learn new software programs.
Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), and/or Certified Clinical Research Professional (CCRP). Prior experience as an industryCRAor Monitor is also preferred.
Hiring department may require certification by an appropriate certifying body within two years of hire.
Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
•Certified Clinical Research Professional (CCRP,CCRCorCCRA)
•Prior experience or knowledge of oncology, and oncology related research
•Prior experience with Institutional Review Board (IRB) procedures
•Strong written and oral communication skills
•An understanding of University operations, policies and technology is preferred. Training or teaching experience is also preferred.
Bachelor’s degree in Health Care Administration, Science, Business Administration or a related field plus five years regulatory or clinical trials experience. Knowledge Federal and International Guidelines (CFRandICH). Proficient with word processing, spreadsheet and related computer applications; demonstrated human relations and effective communication skills also required.
This position is not responsible for providing patient care.
Type Benefited Staff
Special Instructions Summary
The University of Utah is an Affirmative Action/Equal Opportunity employer and is committed to diversity in its workforce. In compliance with applicable federal and state laws, University of Utah policy of equal employment opportunity prohibits discrimination on the basis of race or ethnicity, religion, color, national origin, sex, age, sexual orientation, gender identity/expression, veteran’s status, status as a qualified person with a disability, or genetic information. Individuals from historically underrepresented groups, such as minorities, women, qualified persons with disabilities, and protected veterans are strongly encouraged to apply. Veterans’ preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law.
To inquire about this posting, email: email@example.com or call 801-581-2300. Reasonable accommodations in the application process will be provided to qualified individuals with disabilities. To request an accommodation or for further information about University AA/EO policies, please contact the Office of Equal Opportunity and Affirmative Action, 201 S. Presidents Cr., Rm 135, (801) 581-8365 (V/ TDD ), email: firstname.lastname@example.org .
The University is a participating employer with Utah Retirement Systems (“URS”). To be eligible for retirement contributions, you must be hired into a benefit-eligible position. Certain new hires are automatically assigned to the URS retirement plan and other employees with prior URS service, may elect to enroll in the URS within 30 days of hire. Regardless of whether they are hired into a benefit-eligible position or not, individuals who previously retired and are receiving monthly retirement benefits from URS must notify the Benefits Department upon hire. Please contact Utah Retirement Systems at (801)366-7770 or (800)695-4877 or the University’s Benefits Department at (801)581-7447 for information.
This position may require the successful completion of a criminal background check and/or drug screen.