Clinical Research Coordinator

5 days ago

Albuquerque, New Mexico, United States Medix™ Full time

The Clinical Research Coordinator at Medix™ serves as a seasoned clinical research professional responsible for overseeing the planning, execution, and evaluation of multiple clinical research protocols. This role manages the daily operations of multiple studies, ensuring adherence to regulatory guidelines and sponsor requirements. The incumbent is responsible for mentoring less experienced Clinical Research Coordinators, monitoring and maximizing adherence to research standards, and working closely with study team members to ensure participant safety and protocol adherence.

CORE JOB FUNCTIONS

  • Develops and implements strategies to monitor, document, report, and follow-up on unanticipated occurrences and protocol deviations.
  • Coordinates the implementation of multiple complex clinical research protocols, ensuring synchronization of study visits, procedures, and clinical tests with data collection schedules.
  • Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations.
  • Develops, disseminates, and assures adherence to study-related clinical research best practices and scientific manuals.
  • Provides leadership in protocol implementation and study progress, keeping investigators apprised of study progress.
  • Assumes leadership in identifying and working through ethical conflicts arising during protocol implementation, and refers these conflicts to the Research Ethics Team for consults as needed.
  • Organizes and manages site visits and internal/external auditing activities as assigned.
  • Coordinates research team meetings and assures communications across-the-board.
  • Assures synchronization of study visits/procedures/clinical tests with data collection schedules, established time-points; manages progress of study participants through protocol; expedites overall study progression.
  • Coordinates the compilation of information needed for research reports; peer-reviewed publications; develops strategies to disseminate information to clinical personnel, professional audiences, and stakeholders.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.

CORE QUALIFICATIONS

Education:

Bachelor's degree in a relevant field is required.

Experience:

Minimum 3 years of relevant experience is required.

Knowledge, Skills and Attitudes:

  • Skill in collecting, organizing, and analyzing data.
  • Ability to recognize, analyze, and solve a variety of problems.
  • Ability to analyze, organize, and prioritize work under pressure while meeting deadlines.
  • Ability to process and handle confidential information with discretion.
  • Ability to work independently and/or in a collaborative environment.

Schedule/Shift

Monday to Friday, 8:30am to 5:00pm.

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