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#90014 Clinical Research Coordinator

Extended Review Date: Mon 10/30/2017

This position will remain open until a successful candidate has been identified.

UCSD Layoff from Career Appointment: Apply by 9/15/17 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor. Eligible Disability Counseling and Consulting services (DCC) or Special Selection clients should contact their Vocational Rehabilitation Counselor for assistance.

DESCRIPTION

Under general supervision, the Clinical Research Coordinator will manage and execute clinical trials for the Movement Disorder Center. The Clinical Research Coordinator will provide significant independent contributions as well as original ideas pertaining to the planning and development of studies related to Parkinson’s disease (PD), Dementia and atypical parkinsonian disorders such as: progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), multiple system atrophy (MSA), Lewy body disease and other related disorders.

The Clinical Research Coordinator will:
1) implement and manage all clinical research projects
2) provide direction and guidance in the execution of clinical research
3) propose solutions and strategies to resolve any issues that might arise
4) implement Phase I and II therapeutic clinical trials under the supervision of the principal investigator.

The Clinical Research Coordinator will also handle clinical coordination and testing, protocol management and administration and will act as a liaison with UCSD departments and community clinics/agencies. The incumbent will work closely with state and federal regulatory officials and industry sponsors to ensure compliance with all study-related activities.

MINIMUM QUALIFICATIONS

  • Theoretical knowledge of medical and pharmaceutical terminology and concepts, and/or biological science, with a Bachelor's degree in pharmacy, biology or hematology, sufficient to prepare, review and understand the contents of medical research protocols and amendments.

  • Demonstrated project management experience with the ability to successfully plan, organize, prioritize, develop, analyze, implement and manage multiple pharmacological clinical Phase I and II research projects with complex logistics involving multi-sites and priorities. Ability to set short and long-term goals of projects and project objectives, and work with others in achieving organizational goals and deadlines.

  • Working knowledge of FDA regulations, OPRP, HRPP policies and procedures, and HIPAA. Familiarity with the code of federal regulations (CFRs), Good Clinical Practice (GCP) guidelines and other regulations for the conduct of clinical research.

  • Strong demonstrated experience working with clinical trials research activities, regulatory compliance, guidelines related to informed consent, ethical conduct, and protection of human subjects as well as interpreting and comprehending complex clinical research protocols, activities and guidelines. Proven ability to abstract information from protocol and investigators brochures to create a stand-alone Research Plan.

  • Knowledge of neurological disease such as Parkinson’s disease, dementia, atypical parkinsonian disorders, progressive supranuclear palsy, corticobasal degeneration, multiple system atrophy, Lewy body disease and other related disorders.

  • Proven ability to read, understand, and learn study procedures from protocols. Strong problem-solving and decision-making skills.

  • Experience conducting neuropsychometric test batteries such as Digit Span Forward, Digit Span Backward, Verbal Fluency FAS, Wais-R Digit Symbol Substitution test, Category Fluency test, Trail Making Test and Clock Drawing Test, ADAS-Cog (Certification needed) and the Mini mental Status Exam (MMSEs).

  • Experience creating or modifying Informed Consent documents that comply with HRPP, FDA and other governing agencies.

  • Demonstrated ability to research information, and to develop responsive, creative, innovative, and effective solutions and analyze data to arrive at valid conclusions, recommendations and plans of actions. Detail oriented, logical and methodological approach to problem solving. Strong process orientation.

  • Experience handling human blood samples and working knowledge of protocols for shipping of biological substances. International Air Transportation Association (IATA) certification preferred to oversee shipping of biological substances.

  • Familiarity with cooperative group agencies and trials including experience preparing and submitting a variety of forms related to research protocols in compliance with federal policies and other agencies with ability to pay conscientious attention to detail.

  • Experience and familiarity with the Institutional Review Board (IRB). Experience preparing and submitting continuing review materials, amendments, and other regulatory documents to an IRB.

  • Excellent oral and written communication skills. Proven ability to interact with all organizational levels and to communicate effectively and professionally both in person and via phone. Strong phone etiquette. Ability to present a positive impression in person, on the telephone, and through e-mail.

  • Demonstrated ability to write policies, business correspondence, reports and procedure manuals, experience with editing and/or proofreading documents, fast and accurate typing skills. Excellent grammatical and proof reading skills.

SPECIAL CONDITIONS

  • Must be willing to travel to national meetings.

  • Must be willing to work evenings and weekends as needed per schedule of events/protocol.

  • International Air Transportation Association (IATA) certification preferred to oversee shipping of biological substances.


UC San Diego Health is the only academic health system in the San Diego region, providing leading-edge care in patient care, biomedical research, education, and community service. Our facilities include two university hospitals, a National Cancer Institute-designated Comprehensive Cancer Center, Shiley Eye Institute, Sulpizio Cardiovascular Center, and several outpatient clinics. UC San Diego Medical Center in Hillcrest is a designated Level I Trauma Center and has the only Burn Center in the county. We invite you to join our dynamic team!

 

Applications/Resumes are accepted for current job openings only. For full consideration on any job, applications must be received prior to the initial closing date. If a job has an extended deadline, applications/resumes will be considered during the extension period; however, a job may be filled before the extended date is reached.

 

UC San Diego Health is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, age, protected veteran status, gender identity or sexual orientation. For the complete University of California nondiscrimination and affirmative action policy see: http://www-hr.ucsd.edu/saa/nondiscr.html

UC San Diego is a smoke and tobacco free environment. Please visit smokefree.ucsd.edu for more information.

UC San Diego School of Medicine
Payroll Title:
SRA 3
Department:
NEUROSCIENCES
Salary Range
Commensurate with Experience
Worksite:
East Campus
Appointment Type:
Career
Appointment Percent:
100%
Union:
RX Contract
Total Openings:
1
Work Schedule:
Days, 8 hrs/day