Assoc. Clinical Research Coord Rochester

TALENT Software Services; Rochester (MN); Sur place; USD 52 000 - 68 000; Plein temps

Résumé du poste

TALENT Software Services seeks a detail-oriented clinical research coordinator in Minnesota. This on-site role collaborates with investigators and staff, ensuring compliant execution of research protocols, participant interactions, and data management across multiple studies.

The position emphasizes regulatory duties, protocol development support, and coordination of study logistics with occasional travel. Strong attention to detail and customer-service experience are valued assets.

Qualifications

• One year of clinical research experience.
• Medical terminology course.
• Clinical research experience preferred; customer service or healthcare patient-facing experience accepted.
• Experience coordinating patient-facing activities, scheduling, documentation, and working within regulated environments is helpful.

Responsabilités

• Coordinates non-therapeutic clinical research protocols under PI or supervisor guidance in compliance with regulations.
• May assist in complex studies with direction but not overall responsibility.
• Screens, enrolls, and recruits research participants.
• Coordinates schedules and monitors research activities and subject participation.
• Recognizes adverse events and protocol deviations; reports appropriately and collects/enters data.
• Performs administrative and regulatory duties related to the study as assigned.
• Some travel may be required.
• Supports protocol development and maintenance activities (IRB submissions, study logistics, communications).
• Participates in other protocol development activities and executes other assignments as warranted.

Connaissances

Clinical research

Medical terminology

Patient scheduling

Documentation

Attention to detail

Description du poste

Job Summary

Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Interacts with various departments within the institution. Works cooperatively with other investigators and personnel at all levels. Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.

Job Responsibilities

• Coordinates non-therapeutic (i.e., minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.


• May assist in complex (i.e., interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies.


• Screens, enrolls, and recruits research participants.


• Coordinates schedules and monitors research activities and subject participation.


• Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately. Collects, abstracts, and enters research data.


• Performs administrative and regulatory duties related to the study as assigned.


• Some travel may be required.


• Protocol Development and Maintenance Activities: Responsibilities may include ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (e.g., data collection booklets, use of CRU), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes.


• Participates in other protocol development activities and executes other assignments as warranted and assigned.


• Responsibilities may include participant scheduling, responding to patient communications, supporting blood draw scheduling, kit management, research documentation, and other study coordination activities.

Skills

• See Education Section for Required Experience.

Preferred Skills & Experience

• One (1) year of clinical research experience.


• Medical terminology course.


• Clinical research experience is strongly preferred but would also accept customer service experience or other healthcare patient-facing experience.


• Experience coordinating patient-facing activities, scheduling, documentation, and working within regulated environments is helpful.


• Medical terminology experience is preferred.


• Strong attention to detail is preferred.


• Experience with service excellence doing repetitive tasks.

Schedule Notes

Mon-Fri, 40 hours per week. Flexible start/end times between approximately 7:00 AM and 5:00 PM, on site.