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Experienced Clinical Research Coordinator (CRC) for Dallas Urgent Care

URGENT CARE CLINICAL TRIALS LLC Dallas, TX
  • Expired: over a month ago. Applications are no longer accepted.
Job Description

Job Summary:

  • Manage the clinical research trial process according to specific requirements, regulatory procedures, and protocols. In addition, help to ensure accuracy of data collection, resolution of queries, patient scheduling, management of study drug, data recording and follow up. Care received by research participants is driven by study requirements and the collection of research data as well as clinical indications. Candidate will work with the ultimate goal of ensuring data is collected and documented appropriately.

Primary Job Responsibilities:

  • Work with providers including the Principal Investigator, UCCT staff, site staff, and patients as needed
  • Adhere to the guidelines of FDA GCP/ICH as well as study protocol and company SOPs
  • Coordinate, record and manage subject study data by maintaining accurate and complete source
  • Complete case report forms and queries in a timely manner
  • Perform quality control on subject data thats collected throughout the study
  • Upload data and files to CTMS
  • Oversee and maintain records of the proper receipt, storage, distribution and any shipments or transfer of investigational product.
  • Work with the Principal Investigator, UCCT staff, site staff, patients, Sponsors, CROs and IRBs.
  • Adhere to the guidelines of FDA GCP/ICH as well as study protocol and company SOPs.
  • Complete feasibility questionnaires based on site information as well as complete regulatory start up packages
  • Responsible for patient recruitment including submitting any advertising for sponsor and IRB approval as well as maintaining records of recruitment efforts and screening.
  • Obtain informed consent under the guidance of the PI.
  • Coordinate patient visits from screening to follow up.
  • Ensure subjects meet all inclusion/exclusion criteria and have been properly consented prior to screening and enrollment into any clinical trial.
  • Coordinate, record and manage subject study data by maintaining accurate and complete source.
  • Perform physical assessments such as collecting height, weight, vitals, ECGs, etc…
  • Perform basic lab procedures such as collecting, preparing, and shipping specimens.
  • Communicate with IRBs, Sponsors, CROs, and outside vendors.

Experience and Skills:

  • Associates/Bachelor Degree or/with equivalent experience in a related field or position
  • Knowledge of clinical trials terminology and forms such as 1572, ICFs and SAE reporting
  • Excellent written, computer and verbal communication skills

Preferred Experience:

  • Experience with electronic data capture (EDC) & interactive response systems (IRT)
  • Associates/Bachelor Degree or/with equivalent experience in a related field or position
  • Prefer 2 years of research experience in a clinical research setting, Phase I-IV
  • Current GCP and IATA certification preferred
  • Understanding of HIPAA, federal, state and local laws relating to privacy and consent
  • Knowledge of clinical trials terminology and forms such as 1572, ICFs and SAE reporting preferred
  • Ability to organize and prioritize tasks
  • Works well in a team but is self-driven
Company Description
Urgent Care Clinical Trials (UCCT) is a clinical research Site Management Organization (SMO) that developed the first national Investigative Site Network specifically geared to the urgent care industry. By partnering with local community based, established urgent cares and physician offices, we are able to develop clinical research sites within their practices and provide all the necessary resources to successfully conduct clinical research such as providing clinical trials, regulatory oversight, contract and budget negotiations, daily coordination and onsite management, and much more.

URGENT CARE CLINICAL TRIALS LLC

Why Work Here?

Cutting-Edge Clinical Trials in a representative, modern Urgent Care Setting

Urgent Care Clinical Trials (UCCT) is a clinical research Site Management Organization (SMO) that developed the first national Investigative Site Network specifically geared to the urgent care industry. By partnering with local community based, established urgent cares and physician offices, we are able to develop clinical research sites within their practices and provide all the necessary resources to successfully conduct clinical research such as providing clinical trials, regulatory oversight, contract and budget negotiations, daily coordination and onsite management, and much more.

Address

2909 McKinney Ave
Dallas, TX
USA