Regulatory Coordinator I, Cancer Center (Full Time)
Phase2 Technology, Tucson, AZ, United States
Regulatory Coordinator I, Cancer Center (Full Time)
Posting Number:
req25803
Location:
Tucson Campus, 1515 N Campbell Ave, Tucson, AZ 85724 USA
This Regulatory Coordinator position will provide dedicated clinical trials administration support for ongoing and new developmental efforts in cancer clinical trials research. The role works closely with clinical faculty, disease teams, the University of Arizona Human Subjects Protection Program (IRB), investigators, clinical research staff (nurses, data managers), trial sponsors, and administrative staff. The candidate will develop knowledge in assigned disease areas and serve in a consulting role to new faculty and staff regarding policies and procedures for clinical research.
Benefits include health, dental, and vision insurance; life insurance and disability programs; paid vacation, sick leave, and holidays; tuition reduction for employee and eligible family members; retirement plans; and access to university recreation and cultural activities.
Duties & Responsibilities
Prepare and coordinate IRB and other required submissions and approvals of new Phase I–III protocols for industry, investigator‑initiated, and national cooperative group studies in assigned program areas.
Prepare and coordinate IRB and submissions of protocol amendments, IND safety reports, and progress reports for assigned studies.
Coordinate regulatory activities related to clinical trial start‑up and conduct.
Participate in routine and end‑of‑study monitoring and auditing to ensure compliance with policies, regulations, protocols, and SOPs.
Prepare, coordinate, and maintain regulatory compliance documentation required by agencies and sponsors.
Update the clinical trials management system (CTMS) on study status and actions.
Actively participate in assigned program areas by scheduling and preparing agendas and minutes for meetings.
Other duties as assigned.
Knowledge, Skills, and Abilities
Excellent technical writing skills.
Strong interpersonal, communication, and problem‑solving skills.
Excellent organizational skills.
Proficiency in MS Word and Excel.
Knowledge of medical oncology terminology and treatment concepts.
Minimum Qualifications
Bachelor’s degree or equivalent advanced learning attained through experience.
At least one year of relevant work experience.
Preferred Qualifications
Familiarity with University of Arizona and federal policies and procedures for protection of human subjects.
Previous experience with national cooperative group and private industry cancer clinical research.
Compensation and Benefits
Salary: $47,356–$59,195 (full‑time). Full benefits as described above.
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Posting Number:
req25803
Location:
Tucson Campus, 1515 N Campbell Ave, Tucson, AZ 85724 USA
This Regulatory Coordinator position will provide dedicated clinical trials administration support for ongoing and new developmental efforts in cancer clinical trials research. The role works closely with clinical faculty, disease teams, the University of Arizona Human Subjects Protection Program (IRB), investigators, clinical research staff (nurses, data managers), trial sponsors, and administrative staff. The candidate will develop knowledge in assigned disease areas and serve in a consulting role to new faculty and staff regarding policies and procedures for clinical research.
Benefits include health, dental, and vision insurance; life insurance and disability programs; paid vacation, sick leave, and holidays; tuition reduction for employee and eligible family members; retirement plans; and access to university recreation and cultural activities.
Duties & Responsibilities
Prepare and coordinate IRB and other required submissions and approvals of new Phase I–III protocols for industry, investigator‑initiated, and national cooperative group studies in assigned program areas.
Prepare and coordinate IRB and submissions of protocol amendments, IND safety reports, and progress reports for assigned studies.
Coordinate regulatory activities related to clinical trial start‑up and conduct.
Participate in routine and end‑of‑study monitoring and auditing to ensure compliance with policies, regulations, protocols, and SOPs.
Prepare, coordinate, and maintain regulatory compliance documentation required by agencies and sponsors.
Update the clinical trials management system (CTMS) on study status and actions.
Actively participate in assigned program areas by scheduling and preparing agendas and minutes for meetings.
Other duties as assigned.
Knowledge, Skills, and Abilities
Excellent technical writing skills.
Strong interpersonal, communication, and problem‑solving skills.
Excellent organizational skills.
Proficiency in MS Word and Excel.
Knowledge of medical oncology terminology and treatment concepts.
Minimum Qualifications
Bachelor’s degree or equivalent advanced learning attained through experience.
At least one year of relevant work experience.
Preferred Qualifications
Familiarity with University of Arizona and federal policies and procedures for protection of human subjects.
Previous experience with national cooperative group and private industry cancer clinical research.
Compensation and Benefits
Salary: $47,356–$59,195 (full‑time). Full benefits as described above.
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