Research Compliance Officer

1 week ago


Augusta, Maine, United States InsideHigherEd Full time


Position Overview

Job ID: 275866
Location: Not Specified
Full/Part Time: Full Time
Regular/Temporary: Regular

About the Institution

Our institution is dedicated to fostering innovation in education and healthcare, preparing the next generation of leaders and healthcare professionals. We offer a dynamic environment for over 10,500 students, providing exceptional educational opportunities that integrate technology, arts, and health sciences. Our commitment to groundbreaking research and patient care positions us as a leader in the academic health sector.

Department Overview

The Cancer Research Center is focused on delivering premier cancer research and care that benefits both local and global communities. Our mission is to eradicate cancer through innovative research and patient-centered care. We are committed to assembling expert teams to address the unique needs of each patient, ensuring that our research impacts cancer care standards worldwide.

Role Summary

The successful candidate will engage in advanced administrative and technical functions to support clinical research initiatives. This role includes managing multiple large-scale, multi-center clinical trials that are investigator-initiated and sponsored by federal and industry partners.

Key Responsibilities
  • Develops new clinical trial research protocols for submission to the Institutional Review Board (IRB), ensuring compliance with all relevant regulations and institutional policies.
  • Oversees regulatory activities for the management of existing clinical research protocols, including amendments, financial disclosures, and adverse event reporting.
  • Responsible for the organization and submission of regulatory documents to appropriate platforms, providing support to clinical investigators and staff.
  • Facilitates training for research faculty and staff on compliance best practices and ensures quality control through regulatory inspections of clinical trials.
  • Performs additional duties as assigned to support the overall objectives of the department.


Qualifications

Required:
Master's degree in a relevant field such as chemistry, biology, or health sciences, along with experience in research or clinical trial settings.

OR

Bachelor's degree in a related discipline with a minimum of three years of research or clinical experience, including supervisory responsibilities.

Preferred:
Certification as a Clinical Research Professional or similar credentials.

Skills and Abilities

Proficient understanding of FDA and GCP regulations, along with strong computer skills (Word, Excel, Adobe Acrobat).
Ability to maintain confidentiality and demonstrate excellent communication skills.
Detail-oriented with strong organizational capabilities.

Compensation and Benefits

Salary range: $45,400 - $55,000, commensurate with qualifications.
Comprehensive benefits package available for full-time employees, including health and dental insurance, retirement plans, and paid time off.

Employment Conditions

All candidates must successfully pass a background check prior to employment. Compliance with cybersecurity and privacy policies is essential.

Equal Opportunity Statement

We are an equal opportunity employer, encouraging applications from diverse backgrounds, including individuals with disabilities and veterans.

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