Ortho-Clin Outcome Ctr-Core

Full Time

77898BR

Job Summary

Technical leader with a high degree of knowledge in the overall field and recognized expertise in specific areas; problem-solving frequently requires analysis of unique issues / problems without precedent and / or structure. Will work closely with research leadership to manage programs that include formulating strategies and administering policies, processes, and resources; functions with a high degree of autonomy. Applies extensive knowledge of clinical research protocols and processes to design research projects of large scope and high degrees of complexity.

Meet with department stakeholders to support shared clinical research objectives across sub-specialty sections. Working closely with Research leadership, the position involves the development of guidelines and ensures compliance with clinical study protocols that involve human subjects. Oversees and resolves operational aspects of clinical studies or trials in conjunction with the project teams, post-award team, and in accordance with standard operating procedures and good clinical practice and regulations. May be responsible for finances, clinical operations, and site and vendor selection.

The Clinical Research Analyst 4 manages the accountability and stewardship of financial, and often physical resources in compliance with departmental and organizational goals and objectives. Manage research data functions; Supervise PRO collection and management of subject sample data and specimens with high fidelity; develop and maintain new technologies to efficiently manage data integrity for compliance.

The Clinical Research Analyst 4 will manage, train, and maintain quality control for the Department, following clinical research activities performed by Clinical Research Coordinators: recruit and screen volunteer research subjects; administrator questionnaires, retain and follow subjects with repeated center visits over several months; collect, process and ship biological samples; perform cognitive function tests; data entry and basic data analysis; preparation of data summaries and progress reports.

The CLIN RSCH ANL 4 is responsible for management of the Orthopaedic clinical research program including all site policies and procedures; management and safety of the research subjects seen at the sites; develop strategies that enhance the efficiency of clinical studies with the PIs; develop Standard Operating Procedures (SOPs) for research procedures and biosample processing; generate and lead the maintenance of compliant protocols for the Committee on Human Research at UCSF, IRB and Clinical Trials.gov; independently develop efficient processes for data management of studies conducted at the Orthopaedic Surgery sites; motivate and maintain subject compliance to remain in long-term clinical studies; and develop and maintain relationships with UCSF and non-UCSF vendors.

The final salary and offer components are subject to additional approvals based on UC policy.

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Please note: An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role.

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Department Description

The Department of Orthopaedic Surgery is internationally recognized and has a growing clinical research unit fostering clinical research programs to study treatments that can optimize patient outcomes. We provide expert treatment for all aspects of musculoskeletal injuries including inpatient and outpatient surgical care, rehabilitation, and orthotics and prosthetics. Our physicians have specific training and experience in a broad range of Orthopaedic specialties at multiple campuses.

Required Qualifications

• Bachelor's degree in related area and 5 (five) or more years of relevant experience and / or equivalent experience / training
• 1 or more years of supervisory experience
• Advanced knowledge of clinical research practices and philosophy, and ability to apply knowledge and skills to recommend improvements in methodology. Advanced knowledge of regulatory and financial requirements
• In depth critical thinking skills to evaluate issues and identify a potential solution. Creatively addresses complex or new problems
• Advanced communication skills; including verbal and written, active listening, critical thinking, persuasiveness, advising and counseling skills. Clear and concise communicator
• Advanced interpersonal skills, including but not limited to: problem-solving, teamwork development, leadership with other team members. Works well with others to achieve common goals
• Proven ability to perform all commonly applicable functions in word processing and spreadsheet software. Advanced knowledge of clinical information and documentation application programs. Proven ability utilizing clinical trial management systems
• In depth ability to work collaboratively with other cross-functional teams. In depth ability to interface, collaborate and influence / persuade other members of an extended study team
• Clinical research experience, including recruitment of research subjects and/or PROs

Preferred Qualifications

• Advanced degree preferred
• Clinical Trial Professional certification from a professional society within one year in position
• Previous experience coordinating multicenter research studies
• Previous experience writing and submitting grant proposals
• Previous experience in writing and publishing research manuscripts and journal articles
• Advanced ability to effectively lead one or more projects with competing to meet the demands of a fast-paced and dynamic work environment. Adaptable to quickly changing priorities

About UCSF

The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world's leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.

Pride Values

UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence - also known as our PRIDE values.

In addition to our PRIDE values, UCSF is committed to equity - both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at

Join us to find a rewarding career contributing to improving healthcare worldwide.

Equal Employment Opportunity

The University of California San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.

Organization

Campus

Job Code and Payroll Title

009549 CLIN RSCH ANL 4

Job Category

Research and Scientific

Bargaining Unit

99 - Policy-Covered (No Bargaining Unit)

Employee Class

Career

Percentage

100%

Location

Mission Bay (SF)

Shift

Days

Shift Length

8 Hours

Additional Shift Details

Monday-Friday 40 hours