Clinical Research Assistant
The University of Texas Southwestern Medical 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 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. Data standardization: works with FHIR data structures to improve health information exchange; AI implementation: using data science techniques to evaluate AI models in healthcare application; AI Ethics & Governance - reviewing the explainability, traceability, and ethics of these AI algorithms; recommends and/or initiates new or modified procedures and techniques based upon latest developments in assigned field or analysis of research data; performs computer programming for accumulation and analysis of research data; designs, constructs, repairs, or modifies electronic and/or mechanical equipment or apparatus used in experiments and research projects; assists principal investigator and other professional personnel in writing of reports and papers for publications; performs other duties as assigned. 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 100% coverage for preventive healthcare-no copay 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 Learn more about these and other UTSW employee benefits! EXPERIENCE AND EDUCATION Required 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. #J-18808-Ljbffr
$19.23 - $24.04 per hour
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$90k - $110k
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...will utilize your skills, knowledge, and clinical judgement to provide a high standard of... ...emergency situations based upon clinical research standards. Responsibilities Responsible... ...management systems as assigned by management. Assist with training of new employees, e.g., co...Work at officeLocal areaRemote workNight shift- ...Clinical Research AssociateTo be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol...Local area
- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes. Job Responsibilities Perform site qualification, site initiation, interim monitoring...Interim roleLocal areaImmediate startRemote workFlexible hours
- ...Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with travel). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect...Work at officeRemote workFlexible hours2 days per week
$85k - $130k
...an important member of the Alira Health Clinical team. The CRA is highly motivated and functions... ...compliance, address site questions, and assist with study recruitment, site training,... ...AND LANGUAGES Knowledge of clinical research, ICH GCP and local regulations Knowledge...Contract workInterim roleLocal areaRemote workFlexible hours- ...JOB DESCRIPTION: Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company...Worldwide
$92.32k - $126.94k
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...subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations... ...input to the site selection process. Assists with the coordination of the site budget... ...proficiency. Understanding of clinical research processes and regulations. Certifications...Contract workInterim roleLocal areaRemote work- ...Description Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and... ...identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators...Contract workTemporary workLocal area
- Clinical Research Associate (CRA) IceCure Medical, an innovative medical device company in the field of cryoablation for the destruction of tumors, is seeking a clinical research associate (CRA) who is based in the United States. The ideal candidate will have a background...Work at office
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...Karius is a life science, venture-backed clinical metagenomics company, focused on... ...cell-free DNA circulating in the body to assist physicians to make rapid treatment decisions... ...experience. Three to five years of clinical research monitoring experience, including...Interim roleWork at officeLocal areaRemote work- Abbott Laboratories in Alameda, California is seeking a Clinical Research Associate I to support clinical trials, monitor site activities, and... .... You will collaborate with cross-functional teams, assist with data collection and query resolution, and help maintain...
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