Clinical Research Coordinator

4 weeks ago

Morgantown, United States Medix™ Full time

Clinical Research Coordinator in Morgantown, WV - 26505

Previous Clinical Research Experience is NOT required**


Summary:

Medix is seeking an experienced Healthcare Professional to join a Clinical Research Site in Morgantown, WV (26505). This role is a full time position and will be Monday-Friday, normal business hours.


Responsibilities:

  • Oversees clinical research initiatives, ensuring compliance with organizations Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and regulatory guidelines governing clinical trials. Actively engages with potential participants to ascertain eligibility and secure consent in accordance with study protocols.
  • Coordinates participant visits and related procedures per protocol timelines and team schedules, including managing travel logistics as necessary. Implements reminder communications to optimize participant attendance and adherence. Proactively identifies and reaches out to potential participants and organizes study visit materials.
  • Serves as the primary liaison for participants, providing regular updates on study progress and facilitating communication with other team members as required. Promptly notifies the Principal Investigator of any safety events and manages participant visit scheduling while addressing technical issues as they arise.
  • Collects and records safety event information, preparing documentation for Principal Investigator review. Ensures data integrity by accurately documenting patient visit details in various systems, resolving queries promptly, and completing sponsor's forms in a timely manner.
  • Ensures accurate data collection, entry, and reporting across both Sponsor and Organizations databases. Assists regulatory staff in maintaining necessary documents in compliance with SOPs and regulations.
  • Effectively communicates study requirements to internal and external stakeholders, including sponsors, monitors, Principal Investigators, and participants. Regularly liaises with the Principal Investigator to review study progress, adverse events, and enrollment status.
  • Manages study supplies and disburses participant stipends as needed. Performs study visits and procedures as per protocol requirements, including vital sign measurements, medical history documentation, and questionnaire administration.
  • Responds promptly to study-related queries and documents issues as they arise. If applicable, administers investigational products, manages equipment inventory, and provides patient education on administration procedures.
  • Monitors site compliance with safety reporting protocols, escalating issues as necessary. Contributes to the development of tools, processes, and training to enhance subject safety throughout the clinical study lifecycle.


Additional Details:

Location: Morgantown, WV (26505)

Hours: Monday-Friday; Onsite 5 Days a week; Normal Business Hours

Pay: $20/hr-$25/hr (Dependent on background and experience)

Duration: ~6 month Contract to Hire (~1,040 hours) - contracted probationary period into direct hire/permanent position

Start Date: ASAP

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