Clinical Research Coordinator II, Neurological Surgery
The University of Texas Southwestern Medical Center
Job Summary The Clinical Research Coordinator II will coordinate and manage a portfolio of high‑complexity, investigator‑initiated trials as well as grant and industry‑funded trials in the Department of Neurological Surgery. These trials include investigations into experimental drugs for embolization treatment of sub‑dural hematomas, sonodynamic therapy for glioblastoma, deep brain stimulation for obsessive‑compulsive disorder and depression, functional restoration in paralyzed individuals using brain‑computer interface implants, and complex investigative device trials where the FDA IDE will be held by the principal investigators. Benefits 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 and Experience Bachelor’s degree in a medical or science‑related field Two years of clinical research experience Additional years of experience or an advanced degree may be considered in lieu of education or experience, respectively Preferred Qualifications BLS (Basic Life Support) may be required based on study protocols or affiliate location requirements CPR AED may be required based on study protocols or affiliate location requirements ACRP or SOCRA certification a plus Responsibilities Directly interact with clinical research participants, via telephone, telehealth, or in‑person, as required Maintain regulatory documentation for studies to comply with industry standards, university policies, FDA requirements, and other hospital policies Coordinate and schedule procedures per study protocol; non‑licensed coordinators may pend study order sets with PI oversight Screen, recruit, enroll, and follow subjects according to protocol guidelines; assist with consent processes Coordinate data collection and develop case report forms or other data collection tools Assist in developing and implementing research studies, including writing clinical research protocols Conduct research procedures as per protocol with proper training and check‑offs to maintain scope of service Assist the PI with fiscal management of trials, including budget preparation Monitor patient safety by reviewing records and ensuring reporting per protocol and HRPP standards Perform research billing activities as needed, including linking patient calendars Coordinate data management and collection for national or multiple concurrent research studies Serve as primary liaison/lead in preparing annual reports for federal, state, and/or local agencies on assigned studies Prepare protocols for Institutional Review Board (IRB) submission; submit amendments and continuing review documents as required Provide in‑service training to all study team members and communicate to involved groups Review research study protocols to ensure feasibility requirements of the study Assist in developing website or other social media for marketing/recruiting based on assigned studies Enter data or assist in assembling data for the clinical trial management system, electronic medical record, and/or other required data entry systems Maintain required subject documentation for each study protocol Perform other duties as assigned 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 Statement 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
- ...Job Summary The CRC II will coordinate and manage a portfolio of high‑complexity, investigator... ...funded trials in the Department of Neurological Surgery. These include trials investigating... ...Directly interact with clinical research participants, as required, for non‑...SuggestedFull timeLocal area
- UT Southwestern Medical Center seeks a Clinical Research Coordinator II (CRC II) to manage various high-complexity investigative trials in Neurological Surgery. Key responsibilities include direct participant interaction, coordinating documentation, and ensuring compliance...Suggested
- ...world‑renowned medical and research center, we strive to provide... ...! Job Summary The CRC will coordinate a portfolio of high‑... ...trials in the Department of Neurological Surgery. These include trials investigating... ...related field One year of clinical research experience; May...SuggestedFull timeShift work
- ...The University of Texas Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator II to manage high-complexity clinical trials. This involves overseeing investigator-initiated studies, maintaining regulatory compliance, and ensuring participant safety...Suggested
- UT Southwestern Medical Center in Dallas is seeking a full-time Clinical Research Coordinator to lead a portfolio of complex research trials in the Department of Neurological Surgery. Responsibilities include coordinating regulatory aspects, interacting with research participants...SuggestedFull time
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$32 - $36 per hour
...Job Title: Clinical Research Coordinator II The Clinical Research Coordinator II (Non-RN) plays a key role in all aspects of clinical research, including screening and enrolling participants, coordinating their care and follow‑up, and ensuring strict adherence to regulatory...Contract workTemporary workWork at officeRemote work- Baylor Scott & White Health in Dallas is seeking a Clinical Research Coordinator 2 to assist Principal Investigators in all facets of clinical trials, from pre-study to closure. This position entails detailed responsibilities, ensuring compliance with federal and institutional...
- ...Overview Lead Clinical Research Coordinator, Psychiatry Molecular Imaging - (904445) Lead Clinical Research Coordinator, Psychiatry Molecular Imaging... ...studies investigating brain chemistry in psychiatric and neurologic disorders. This role involves coordinating participant...Full timeLocal area
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- ...way into the future of medical discovery through world‑class clinical research. At Dallas Research Institute, we are committed to driving... ..., appointment scheduling, records review, treatment coordination, and collecting vital signs. Complete documentation and data...Work at officeLocal areaFlexible hours
- ...part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.The Clinical Research Coordinator is responsible for the planning, coordination, and execution of clinical research studies, including the collection and...Permanent employmentInterim roleWork visaFlexible hours
- ...Job Details: Job Location: Dermatology Treatment and Research Center (DTRC) - Dallas, TX 75230 Position Type: Full Time Education... ...and excellent interpersonal skills for the position of clinical research coordinator. Clinical research coordinators are responsible for...Full timeContract workShift work
- ...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Clinical Research Prescreen Coordinator FullTime Zenos/Dallas, Dallas, TX, US 30+ days ago Requisition ID: 1260 About the Role The Pre‑Screening...Full timeH1bWork at office
$56.16k - $76.96k
...talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support... ...difference in your career! As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support...Temporary workFlexible hours$51k - $74k
...POSITION SPECIFICSThe Penn State College of Medicine, Department of Family & Community Medicine, in Hershey, PA, is seeking a Clinical Research Coordinator. Penn State College of Medicine (PSCOM) is one (1) of six (6) participating institutions in a large, six-site nationwide...Full timeWork experience placementWork at officeRemote work- ...Clinical Research Coordinator Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in advancing patient care through high-quality, hospital-based clinical trials. The position involves coordinating...Weekend workWeekday work
$28 - $33 per hour
...Clinical Research Coordinator - Dallas We are seeking a dedicated and skilled Clinical Research Coordinator to join our team in Dallas. In this role, you will engage with research investigators, pharmaceutical companies, and contract research organizations, as well...Contract workTemporary work- EmVenio is seeking a Clinical Research Coordinator to provide support to clinical operations teams and ensure regulatory compliance in patient engagement. This role demands attention to detail while managing multiple studies and tasks collaboratively with team members....Work at office
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- Direct Jobs is looking for a Clinical Research Coordinator 1 to assist Principal Investigators with all phases of clinical trials in Dallas, Texas. This entry-level position involves implementing research protocols, ensuring compliance with guidelines, and conducting quality...
- UT Southwestern Medical Center is seeking a Clinical Research Coordinator I PRN in Dallas, Texas. This role involves coordinating patient participation in clinical research studies, data management, and ensuring data quality for complex research projects. Candidates must...Relief
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