Clinical Research Coordinator - Early Phase Program

Clinical Research Coordinator - Early Phase Program

HDF Comprehensive Cancer Ctr

Full Time

77202BR

Job Summary

The Early Phase program has a multi-disciplinary team that works closely with patients, providing the resources and close cooperation of many specialists with deep expertise in diagnosing and treating early and late- stage cancer.

Our physician-scientists are also researching and developing new and effective treatments for cancer, including clinical trials.

The Early Phase program is seeking a Clinical Research Coordinator with an interest in investigational drugs to have oversight over multiple clinical research projects and support our growing program.

The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and / or the Associate Director of Clinical Research Programs for the Early Phase program.

The CRC will coordinate the administrative, data, and patient scheduling operations of several concurrent clinical research studies under the guidelines of research protocols and regulatory policies.

The CRC will assist in the care of early and late-stage cancer patients while they participate in phase 1 and phase 2 clinical trials.

In the role, the CRC will attend clinic appointments, follow test results, and assist in ordering appropriate study-related procedures / tests.

The CRC will have the opportunity to learn certain aspects of oncology including but not limited to prevention, early detection, treatment / medication management, and end of life care for cancer patients.

The CRC's duties may include, but will not be limited to, supporting the management and coordinating the tasks of single or multiple clinical research studies.

• This involves coordinating study required procedures and treatments for study patients; managing and updating databases to insure data integrity;
• acting as intermediary between sponsors, research staff, and various UCSF departments; assuring compliance with all relevant regulatory agencies;
• assisting Clinical Research Manager, Associate Director of Clinical Research Programs and / or PI with research tasks; maintaining relevant regulatory documents in partnership with the Regulatory department;
• reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols;

and performing other duties as assigned.

Note : This position requires a physical / health screening.

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

To see the salary range for this position (we recommend that you make a note of the job code and use that to look up) : TCS Non-Academic Titles Search (https : / / tcs.

ucop.edu / non-academic-titles)

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.

For roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range.

To learn more about the benefits of working at UCSF, including total compensation, please visit : https : / / ucnet.universityofcalifornia.

edu / compensation-and-benefits / index.html

Department Description

The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is one of only two cancer centers in the Bay Area to receive the prestigious designation of "comprehensive" from the National Cancer Institute (NCI).

The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits : laboratory research into the causes of cancer progression;

clinical research to translate new knowledge into viable treatments; compassionate, state-of-the-art patient care; and population research that can lead to improvements in prevention, early detection, and quality-of-life for those living with cancer.

The twin pillars of precision medicine and precision population health guide research and treatment at HDFCCC.

Required Qualifications

• HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
• Attention to detail; strong interpersonal skills; excellent, Required effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions;

and the ability to multi-task in a fast-paced environment while working with a diverse subject population.

• Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.
• Demonstrated knowledge and understanding of research, especially in the areas of biological sciences.
• Prior experience with various computer programs (Microsoft Office; internet-based databases) and using specialized software such as OnCore.
• Ability to sit and work at a computer for several hours per day.
• May need to travel between one or more campuses via UCSF shuttle.
• Ability to stand for several hours of the day.
• Experience in clinical research or demonstrated research or training experience that translates into a clinical research setting.
• Working knowledge of federal, state, and local research regulations and guidelines, and research practice methods in a laboratory or clinical setting.
• Ability to apply relevant information to the assessment, interpretation, and processing of medical data.
• Ability to independently interpret and apply policies, respond to requests, resolve issues, and provide assistance to faculty and staff at all levels in a team- oriented environment.

Preferred Qualifications

• Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system.
• Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.
• Experience with electronic medical records.
• Knowledge of location specific and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the location's mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.).
• Ability to work with a sensitive population of patients (oncology patients).
• Prior analytical and writing skills in a science / research environment.
• Knowledge of clinical research in oncology.
• Knowledge and experience in managing oncology clinical trials.
• Membership in a clinical research professional society.
• Knowledge of medical terminology, research policies and guidelines, guidelines for packing / shipping infectious substances, database building / analysis, and data management within some of the following : Access, Stata, SASS / SPSS, and Teleform programming platforms.
• Experience applying the following regulations and guidelines : Good Clinical Practice Guidelines, Health Information and Accountability Act (HIPAA), The Protection of Human Research Subjects, CHR regulations for recruitment and consent of research subjects, Effective Cash Handling Procedures, Environmental Health and Safety Training, Fire Safety Training.

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 diversity.ucsf.edu

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

009335 CLIN RSCH CRD

Job Category

Research and Scientific

Bargaining Unit

University Professional Technical Employees - Research Support Professionals Unit (UPTE-RX)

Employee Class

Career

Percentage

100%

Location

Mission Bay (SF), Parnassus Heights (SF)

Shift

Days

Shift Length

8 Hours

Additional Shift Details

Monday - Friday