OVERVIEW

The Clinical Research Coordinator plays a pivotal role in the management and execution of clinical trials, ensuring compliance with regulatory requirements and adherence to Good Clinical Practice (GCP). This position is essential for facilitating the smooth operation of clinical studies, from patient recruitment to data collection and documentation. The ideal candidate will possess a strong understanding of clinical development processes and be dedicated to advancing medical research.
This position requires an RN background or Unblinded CRC experience. Please do not apply unless you have this experience.

SKILLS

• Strong knowledge of clinical trials management and clinical development processes.
• Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Proficiency in patient monitoring techniques and blood sampling procedures.
• Experience in documentation review to ensure compliance with study protocols.
• Ability to utilize statistical software for data analysis purposes.
• Excellent organizational skills with attention to detail in managing multiple tasks simultaneously.
• Strong interpersonal skills for effective communication with patients and team members.
  This role is ideal for individuals passionate about contributing to the advancement of medical science through rigorous research practices while ensuring the highest standards of patient care and ethical conduct in clinical trials.
  Job Type: Full-time
  Pay: $55,060.00 - $71,385.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Ability to Commute:

• Plano, TX 75024 (Required)

Ability to Relocate:

• Plano, TX 75024: Relocate before starting work (Required)

Work Location: In perso

• Coordinate and oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment.
• Ensure compliance with HIPAA regulations and maintain patient confidentiality throughout the study process.
• Monitor patient progress and safety during clinical trials, conducting blood sampling as necessary.
• Manage clinical trial documentation, including informed consent forms, case report forms, and regulatory submissions.
• Review documentation for accuracy and completeness to ensure adherence to study protocols.
• Collaborate with clinical laboratory personnel to facilitate laboratory testing and sample processing.
• Utilize statistical software for data analysis and reporting of study results.
• Maintain effective communication with study sponsors, investigators, and other stakeholders involved in the research process.