Clinical Research Assistant II, Cancer Center
Dallas, Texas
Employer: UT Southwestern Medical Center
Industry: Research & Laboratory
Salary: Competitive
Job type: Full-Time
Clinical Research Assistant II, Simmons Comprehensive Cancer Center
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 patients and employees. With over 20,000 employees, we are committed to continuing our growth with the best professionals in the healthcare industry. We invite you to be a part of the UT Southwestern team where you'll discover teamwork, professionalism, and consistent opportunities for growth. Join UT Southwestern to help with our mission to educate, discover and heal through our life-changing research!
Job Summary
The Simmons Cancer Center has an opening for a Clinical Research Assistant II to join their Gastrointestinal Disease Oriented Team. The ideal candidate understands visit schedules, inclusion/exclusion criteria and protocol requirements for low complexity trials (e.g., questionnaire, data registry, scripted). This role schedules research visits; assists research staff by completing research protocol related tasks; reviews and abstracts information from medical records including eligibility criteria; enters data into case report forms or other data collection system based on research study; assists with maintenance of study level documentation; assists with data queries and possible edits for accuracy; compiles data for regulatory requirements and /or deadlines for local or sponsor submissions; maintains existing databases and ensures data integrity. This position is eligible for a hybrid work schedule.
Experience and Education
Minimum Requirements
May perform some or all of the following based on research study:
Knowledge of applicable Federal and institutional regulations governing clinical research. Knowledge of clinical research protocols. Effective organizational skills and attention to detail. Proactively works to maximize results of the team and organization. Follows and understands the regulations for Protected Health Information (PHI). Proactively works to maximize results of the team and organization. Possess strong computer skills (spreadsheets, databases, and interactive web-based software). Possess good communication skills. Possess the ability to problem solve. Work requires ability to conduct interviews with research subjects.
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. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.
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 patients and employees. With over 20,000 employees, we are committed to continuing our growth with the best professionals in the healthcare industry. We invite you to be a part of the UT Southwestern team where you'll discover teamwork, professionalism, and consistent opportunities for growth. Join UT Southwestern to help with our mission to educate, discover and heal through our life-changing research!
Job Summary
The Simmons Cancer Center has an opening for a Clinical Research Assistant II to join their Gastrointestinal Disease Oriented Team. The ideal candidate understands visit schedules, inclusion/exclusion criteria and protocol requirements for low complexity trials (e.g., questionnaire, data registry, scripted). This role schedules research visits; assists research staff by completing research protocol related tasks; reviews and abstracts information from medical records including eligibility criteria; enters data into case report forms or other data collection system based on research study; assists with maintenance of study level documentation; assists with data queries and possible edits for accuracy; compiles data for regulatory requirements and /or deadlines for local or sponsor submissions; maintains existing databases and ensures data integrity. This position is eligible for a hybrid work schedule.
Experience and Education
Minimum Requirements
- High School and 2 years of experience. OR
- Associate's degree in medical or science related field and 1 year of experience. OR
- Bachelor's degree in medical or science related field and no prior experience.
- A minimum of Heart Saver for non-licensure or BLS for Licensure may be required based on affiliate location requirements.
May perform some or all of the following based on research study:
- Understands visit schedules, inclusion/exclusion criteria and protocol requirements for low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits.
- Assists research staff by completing research protocol related tasks.
- Reviews and abstracts information from medical records including eligibility criteria.
- Enters data into case report forms or other data collection system based on research study.
- Assists with maintenance of study level documentation.
- Assists with data queries and possible edits for accuracy.
- Compiles data for regulatory requirements and /or deadlines for local or sponsor submissions.
- Maintains existing databases and ensures data integrity.
- Performs QA/QC clinical analysis and data checks using various databases based on trial.
- Assists with preparing annual reports and/or modifications to institutional review board (IRB).
- This may include reportable events (UPIRSO).
- Assist and prepare research records for formal sponsor audits or internal audits.
- Recruits and enrolls patients in research study that may include consenting patients after training and with supervision.
- With adequate training and supervision, assists with participant screening and recruitment for more complex trials.
- Conducts and documents consent for participants in studies.
- Assists with the development of consent plans and documents for participants.
- Identifies incomplete, inaccurate, or missing data for more complex studies and works with lead coordinator to correct errors.
- Assists with ordering and maintaining research supplies following university/department procedures, ensuring that equipment is in good working order.
- With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols.
- Assists in preparing studies for closeout, (e.g. packing files, documenting files for storage, shipping extra supplies back to sponsor).
- With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG's needed for research study.
- Based on research study, other procedures/equipment/services may be required.
- May perform patient care (basic skills) under the direction of PI following scope of work document.
- 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 of applicable Federal and institutional regulations governing clinical research. Knowledge of clinical research protocols. Effective organizational skills and attention to detail. Proactively works to maximize results of the team and organization. Follows and understands the regulations for Protected Health Information (PHI). Proactively works to maximize results of the team and organization. Possess strong computer skills (spreadsheets, databases, and interactive web-based software). Possess good communication skills. Possess the ability to problem solve. Work requires ability to conduct interviews with research subjects.
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. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.
Created: 2024-08-22
Reference: 810052
Country: United States
State: Texas
City: Dallas
ZIP: 75287
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