Clinical Research Coordinator II, Cancer Center

Clinical Research Coordinator II, Simmons Comprehensive Cancer Center, Cancer Research

Why UT Southwestern?

With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. As the only National Cancer Institute-designated comprehensive cancer center in North Texas, we invite you to continue your healthcare career with us at Harold C. Simmons Comprehensive Cancer Center. You'll discover a magnet facility with a culture of teamwork, professionalism, and consistent opportunities for learning and advancement into leadership roles.

Job Summary

The Simmons Cancer Center is seeking a Clinical Research Coordinator II to join the Melanoma/Sarcoma/Head & Neck team. This role works under the direction of an Investigator(s) with general supervision, to coordinate research projects. Additionally, this position performs patient/participant coordination, such as screening, consenting, and following up with Melanoma/Sarcoma/Head & Neck clinical trial patients, as well as data management. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.

Experience and Education

Minimum Requirements

• Bachelor's degree in medical or science related field and two years clinical research experience. May consider additional years of experience or advanced degree in lieu of education or experience, respectively.
• ACRP or SOCRA certification a plus.
• A Heart Saver for non-licensure or BLS for Licensure may be required based on research study protocols or affiliate location requirements.

Job Duties

May perform some or all the following:

• Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Interacts via telephone, telehealth or in-person.

• Coordinates regulatory documentation for research studies that includes maintaining information to comply with industry standards, University policies, FDA requirements or other hospital policies.

• Coordinates and schedules procedures as per research study.

• A non-licensed coordinator may pend study order sets with oversight by PI.

• Screens, recruits, enrolls and follows subjects according to research protocol guidelines (non-clinical and clinical procedures).

• May also assist with the consent processes.

• Maintains and coordinates data collection information required for each study that may also include developing CRF's (case report form) or data collection tools.

• Assists in developing and implementing research studies, may include writing clinical research protocols. Conducts research procedures according to the protocol with proper training and check offs to maintain scope of service.

• May assist the PI on the fiscal management of the trial including budget preparation.

• Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards.

• May perform research billing activities, as needed, based on size of department (including linking patient calendars).

• Coordinates data management and collection for national (larger/more complex) research studies or multiple research studies at a given time.

• Serves as primary liaison/lead in preparing annual reports for federal, state, and or/or local agencies on assigned studies. Prepares protocols for Institutional Review Board (IRB) submission.

• May also submit amendments and continuing review documents.

• Provides in-service training to all study team members and communicates to involved groups.

• Reviews research study protocols to ensure feasibility requirements of the study.

• Assists in developing website or other social media for marketing/recruiting based on assigned clinical research study.

• Enters data or assists in assembling data to enter in the assigned clinical trial management system, electronic medical record and/or other required data entry systems.

• Maintains required subject documentation for each study protocol.

• Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.

• Performs other duties as assigned.

Knowledge, Skills & Abilities

Work requires knowledge of basic and clinical research terminology, regulations, and procedures. Work requires strong computer skills (spreadsheets, databases, and interactive web-based software). Work requires ability to communicate effectively with various levels of internal and external contacts. Work requires ability to work with confidential information on daily basis Proactively works to maximize results of the team and organization Follows and understands the regulations for Protected Health Information (PHI) Work requires good communication skills. Work requires the ability to problem solve.

Working Conditions

Work is performed primarily in an office environment but may require periodic visits to clinical and off-site clinical areas for purpose of interviewing patients. May require local or out-of-state travel based on research study.

To learn more about the benefits UT Southwestern offers visit https://www.utsouthwestern.edu/employees/hr-resources/

For general COVID-19 information, applicants should visit https://www.utsouthwestern.edu/covid-19/work-on-campus/

This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information. UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. In accordance with federal and state law, the University prohibits unlawful discrimination, including harassment, on the basis of: race; color; religion; national origin; sex; including sexual harassment; age; disability; genetic information; citizenship status; and protected veteran status. In addition, it is UT Southwestern policy to prohibit discrimination on the basis of sexual orientation, gender identity, or gender expression.