Clinical Research Assistant II

The University of Texas Southwestern Medical Center

Dallas (TX)

On-site

USD 45,000 - 60,000

Full time

4 days ago
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Benefits offered by this job

PPO medical plan
Paid Time Off
TRS retirement program
Paid parental leave
Tuition reimbursement

Job summary

The University of Texas Southwestern Medical Center is hiring a Clinical Research Assistant II to support data management for local and national studies and coordinate study visits. You will interact with patients and clinical staff and assist with specimen handling and regulatory tasks.

Candidates with bilingual English/Spanish skills are highly encouraged to apply, and prior clinical research experience is preferred.

Qualifications

  • Experience in clinical research data management and data entry.
  • Ability to communicate effectively with clinical staff and patients.
  • Bilingual English and Spanish is highly encouraged.

Responsibilities

  • Support data management for local and national studies under supervision.
  • Enter data into case report forms and maintain study documents.
  • Coordinate with PI, CRAs and clinical staff for visits and sample collection.
  • Maintain data integrity and assist with regulatory submissions and audits.
  • Recruit and consent participants; assist with screening for appropriate trials.
  • Assist with phlebotomy, vital signs, and EKGs as required by the study.

Education

High School Diploma
Associate's Degree
Bachelor's Degree

Job description

Job Description - Clinical Research Assistant II (972818)

Job Description

Clinical Research Assistant II - ( 972818 )

Description

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. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report , we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!

JOB SUMMARY

Works under the direction of an Investigator(s) with general supervision, to provide ongoing data management for local and national research studies and may coordinate observational (non-treatment/treatment) trials/studies. May provide supporting role for more complex studies under the direction of the PI, Clinical Research Coordinator and/or Clinical Research Lead.

The Simmons Comprehensive Cancer Center is looking to hire a Clinical Research Assistant II who would like exposure to the clinical research field. Our core facility collects human biospecimens which are used by faculty on campus for their research. In this role you will work in a fast-paced environment and interact with patients and clinical staff at UT Southwestern and Parkland Hospitals. In addition to the standard duties below, you will communicate with clinical, surgical and pathology staff regarding timely research specimen collection. You will also be explaining the purpose of the cancer center biorepository to patients and consenting those who agree to participate. Candidates who are bilingual in English and Spanish are highly encouraged to apply.

BENEFITS

UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

  • PPO medical plan, available day one at no cost for full-time employee-only coverage
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer
  • Education
    High School Diploma or
    Associate's Degree in medical or science related field or
    Bachelor's Degree medical or science related field and no prior experience
  • Experience
    2 years experience with High School Diploma or
    1 year experience with Associate's Degree
Preferred
  • Licenses and Certifications
    (BLS) BASIC LIFE SUPPORT may be required based on affiliate location requirements.
    (CPRAED) CPR AED may be required based on affiliate location requirements.
JOB DUTIES
  • Understands visit schedules, 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.
SECURITY AND EEO STATEMENT
Security

This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.

EEO

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.

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; gender, including sexual harassment; age; disability; citizenship; and veteran status. In addition, it is UT Southwestern policy to prohibit discrimination on the basis of sexual orientation, gender identity, or gender expression.

Copyright 2017.The University of Texas Southwestern Medical Center5323 Harry Hines Blvd., Dallas, Texas 75390Phone 214-648-3111

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