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Clinical Research Coordinator Assistant presso NEUROLOGY CONSULTANTS OF DALLAS P A

NEUROLOGY CONSULTANTS OF DALLAS P A · Dallas, Stati Uniti d'America · Onsite

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Job Details

Job Location:    8390 LBJ FREEWAY SUITE 1000 - DALLAS, TX
Position Type:    Full Time
Salary Range:    Undisclosed

Description

The Clinical Research Coordinator Assistant (CRCa) plays a vital role in supporting clinical trial operations, with a strong focus on participant recruitment and investigational drug preparation. This role also assists with screening and scheduling participants, maintaining regulatory and study documentation, preparing supplies for study visits, and ensuring proper handling and accountability of study medications. The ideal candidate is a certified Pharmacy Technician who is detail-oriented, organized, and capable of working in a fast-paced, compliance-driven environment. This position plays a key role in ensuring smooth study execution and participant safety across all phases of clinical research.

 

This position supports clinical research activities in clinical and hospital settings. The qualified candidate will be required to undergo hospital credentialing.

Qualifications


Duties/Responsibilities

  • Communicates clearly with study investigators, sponsors, PI, IRB, and others regarding study protocols, recruitment, adverse events, etc.
  • Participant Recruitment & Screening
    -Assist in identifying, contacting, and pre-screening potential study participants.
    -Schedule and coordinate initial screening and follow-up visits.
    -Maintain accurate and confidential participant records and communication logs.
    -Help prepare and distribute study recruitment materials in compliance with IRB guidelines.
  • Investigational Product Preparation & Handling
    -Prepare, label, and dispense study medications according to protocol requirements and Good Clinical Practice (GCP) guidelines.

-Maintain accurate inventory logs of investigational drugs and related supplies.

-Ensure proper storage, handling, and documentation of all investigational products.

-Collaborate with pharmacy and study teams to ensure drug accountability and compliance.

  • Study Support & Administrative Tasks

-Enter data into electronic data capture (EDC) systems and other study-related databases with a high degree of accuracy.

-File, organize, and maintain regulatory and study documents in both physical and electronic formats.

-Assist with preparation and setup for participant visits and study monitoring visits.

-Support the coordination of study supplies, lab kits, and visit-related materials.

-Perform general administrative duties as needed to support study activities.

  • Ensures compliance and ethical standards are maintained throughout the conduct of the study.
  • Abides by all HIPAA and confidentiality regulations and policies.
  • May require occasional evening or weekend work depending on study needs.
  • Provides any other duties and responsibilities as determined by management and physician leadership.

 

Required Skills/Abilities

  • Must be attentive to detail
  • Demonstrate a strong history of working in a team environment
  • Ability to multi-task
  • Have strong communication skills and customer service

 

Education and Experience

  • Certified Pharmacy Technician (CPhT) – active and in good standing
  • High School Diploma or GED
  • Post-secondary education in healthcare or life sciences is a plus
  • 1+ year experience in pharmacy, clinical, or research setting
  • Knowledge of medication preparation, dispensing, and inventory procedures

 

Physical Requirements

  • Ability to lift up to 30 pounds with frequent lifting and/or carrying of objects weighing 10 pounds
  • Ability to walk and/or stand for significant amounts of time
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