Associate Clinical Research Coordinator - Dr Ehlers Lab

Mayo Clinic • Phoenix, AZ

3d

About The Position

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.

Position Overview:
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,
but are not limited to: ongoing management of the protocol document and process
through editing, amendments, proofing, coordination of study logistics (i.e.
data collection booklets, use of CRU, etc.), 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.

Other job duties:

Participate in upkeep of lab equipment and scheduled maintenance.

Maintain lab inventory to ensure replacement of equipment as needed.

Motivated individuals will be provided opportunities to contribute to data
analysis and dissemination through published manuscripts and local or national
presentations

Responsibilities

• Coordinates non-therapeutic clinical research protocols
• 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
• Ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics
• Institutional Review Board (IRB) submission
• Communication with study sites and/or federal agencies regarding study status changes
• Participate in upkeep of lab equipment and scheduled maintenance
• Maintain lab inventory to ensure replacement of equipment as needed
• Contribute to data analysis and dissemination through published manuscripts and local or national presentations

Benefits

• Medical: Multiple plan options.
• Dental: Delta Dental or reimbursement account for flexible coverage.
• Vision: Affordable plan with national network.
• Pre-Tax Savings: HSA and FSAs for eligible expenses.
• Retirement: Competitive retirement package to secure your future.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees