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Clinical Research Coordinator C

Job in Woodworth, Rapides Parish, Louisiana, 71485, USA
Listing for: University of Pennsylvania
Full Time position
Listed on 2026-09-26
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 54000 - 73000 USD Yearly USD 54000.00 73000.00 YEAR
Job Description & How to Apply Below
Location: Woodworth

University Overview

The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn’s distinctive interdisciplinary approach to scholarship and learning.

As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America’s Best Large Employers in 2023.

Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play.

The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.

Posted Job Title

Clinical Research Coordinator C

Job Profile Title

Clinical Research Coordinator C

Job Description Summary

The Traumatic Brain Injury Research Initiative within the Department of Neurology (TBIRI) is seeking an experienced, adaptable Clinical Research Coordinator C to independently coordinate and execute multiple investigator-initiated and industry-sponsored studies involving acute and chronic traumatic brain injury. TBIRI conducts innovative research involving neuroimaging, blood biomarkers, neuropsychological assessment, pharmacological and device interventions, and other emerging technologies.

Job Description

The CRC-C will function as a senior member of a multidisciplinary research team and will report directly to the TBIRI Program Lead under the supervision of the TBIRI Principal Investigators. This position requires a high degree of independence, organization, flexibility, and clinical research judgment within a fast-paced and dynamic environment where priorities may shift quickly based on patient availability, clinical status, and time-sensitive study requirements.

A central component of the role is direct interaction with patients with brain injury and their families. The CRC-C must demonstrate strong situational awareness and interpersonal judgment, including the ability to “read the room,” recognize when and how to approach patients and families, and adapt communication style, timing, and tone to sensitive or complex situations.

The CRC-C will independently conduct study activities throughout the research lifecycle, including screening, recruitment, informed consent, study visits, assessments, biological sample collection and processing, data collection, longitudinal follow-up, and regulatory maintenance. The position will also support study start-up and closeout, monitoring and audit preparation, study documentation and tracking, and other administrative and operational needs.

As a senior coordinator, the CRC-C will serve as a resource to CRC A/B-level staff and assist with onboarding, study-specific training, and ongoing development. The coordinator will be expected to proactively identify and resolve day-to-day operational and regulatory issues, maintain compliance with study protocols and applicable regulations, and appropriately elevate significant concerns to the Program Lead or…

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