Clinical Research Coordinator
On-site · Brownsville, Texas, United States
Job Summary
Coordinate clinical trials by managing day-to-day operations, recruiting and screening participants, ensuring adherence to study protocols and regulatory requirements (FDA, ICH GCP, HIPAA), documenting and reporting study activities, and reporting participant status. The role requires organized multitasking, excellent communication, and collaboration with sponsors, external vendors, and team members. Responsibilities include conducting assessments (informed consent, medical history, adverse events, Fibroscan, memory screens), data management, liaison with sponsors, enrollment tracking, and maintaining regulatory documents. Travel may be required; bilingual Spanish and English skills are preferred; a proactive, problem-solving mindset and attention to participant care are essential.
Required Qualifications
- High school diploma or general education degree (GED) required
- Bachelor’s Degree in a scientific area of study preferred or equivalent combination of education, training, and experience
- 1 year of experience as a Clinical Research Assistant or Coordinator
- 1-2 years of experience in Clinical Research
- Proficient in all Microsoft Office applications and Clinical Research IO (CRIO) or equivalent CTMS
- Must have strong knowledge of ICH/GCP guidelines
- Must complete GCP training before interacting with participants and must recertify every 2 years or as applicable
- Trained and certified in the administration of Fibroscan and memory screens as required by the study portfolio and individual experience. Training to be provided
- Must have basic life support (BLS) training, provided during onboarding
- Demonstrated organizational skills and outstanding time management, including keen attention to detail, with the ability to track multiple projects at one time
- Strong written and oral communication skills
- Knowledge of basic medical terminology
- Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission
- Comply with the company policies, code of ethics, and guiding values always
- Proficient in Spanish and English preferred
- Certificates and Licenses: Valid Driver’s License
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