Clinical Research Supervisor - req# 38124
University of New Mexico · Albuquerque, NM
FULL-TIME
Posted Oct 2, 2026
Job Description
Clinical Research Supervisor
Requisition ID
req38124
Working Title
Clinical Research Supervisor
Position Grade
11
Position Summary
The University of New Mexico Health Sciences Center Pediatrics Department encompasses a statewide network of hospitals, clinics, and community-based services dedicated to advancing pediatric health through clinical excellence, education, and research. Within this system, the Pediatric Hematology/Oncology division provides the only comprehensive pediatric cancer and blood disorders program in New Mexico, offering a unique opportunity to support clinical, academic, research, and community-facing work.
The Clinical Research Supervisor coordinates, oversees, and quality-controls the execution of federally regulated clinical research studies, including multi-site pediatric oncology, hematology, hemophilia, and translational research trials. This position ensures full compliance with IRB/Human Research Review Committee (HRRC) requirements, Good Clinical Practice (GCP), federal/state regulations, institutional policies, and grant/contract parameters.
The supervisor provides day-to-day technical leadership, administrative oversight, and direct supervision of one staff member—a Research Technician 2—who supports data collection, biospecimen handling, and study coordination tasks. The role is responsible for operational strategy, workflow development, regulatory oversight, and ensuring accurate, reliable, and timely research data and biospecimen management.
The Clinical Research Supervisor collaborates closely with clinical investigators, IRB staff, national research organizations, study sponsors, and internal partners to ensure the smooth and efficient operation of all research, regulatory, and data collection activities. Duties include reviewing case report forms and source documents for completeness, accuracy, and compliance; initiating corrective actions; ensuring timely submission of research data; monitoring patient response to treatment as defined by protocol; and coordinating transmission of clinical data to national research organizations. This position is integral to sustaining high-quality research operations and advancing the mission of pediatric cancer and hematology research at UNM.
Duties and Responsibilities Include but are not limited to:
Supervision, Leadership & Operations
• Provides day-to-day technical leadership and direct administrative supervision to one Research Technician 2, including training, work allocation, productivity oversight, and performance evaluations.
• Plans, organizes, and oversees daily operations of the research unit, including protocol implementation, workflow design, systems development, and quality assurance.
• Develops operating goals and objectives and implements systems, procedures, and process improvements to enhance operational efficiency.
• Ensures appropriate scheduling and utilization of research resources, facilities, and equipment.
Regulatory & Compliance
• Ensures compliance with IRB/HRRC requirements, GCP guidelines, FDA regulations (as applicable), OSHA standards, and all federal, state, and institutional policies.
• Oversees development, submission, and maintenance of IRB applications, amendments, continuing reviews, deviations, and reportable events.
• Maintains regulatory documentation, study records, and essential documents in accordance with audit-ready standards.
Protocol Execution & Quality Control
• Supports investigators in study design, protocol development, and implementation.
• Oversees execution of multiple complex clinical research protocols, ensuring adherence to study timelines, visit windows, and data requirements. As well as consent/enrollment to both Therapeutic and Non-Therapeutic studies
• Develops, implements, and evaluates research and data collection methodologies, systems, and tools appropriate to pediatric oncology and hematology research.
• Reviews source data, case report forms, and eCRFs for accuracy, reliability, and protocol compliance; addresses deficiencies and initiates corrective action.
• Monitors and records patient responses to treatment as defined by protocol and coordinates data communication with investigators and sponsors.
Data & Specimen Management
• Coordinates data compilation, quality control, and preliminary analysis; ensures validity and accuracy prior to submission.
• Oversees and performs (as needed) the processing, tracking, and shipping of blood and human tissue samples in compliance with biosafety and shipping regulations.
• Ensures accurate transmission of clinical research data to national research organizations and sponsors.
Administrative & Financial
• Participates in budget development, cost tracking, and grant/contract administration.
• Ensures research billing compliance and alignment with coverage analyses for therapeutic and non-therapeutic trials.
• Documents operational activities, prepares reports, and supports audit and monitoring visits.
• Performs miscellaneous job-related duties as needed to support research growth and program demands.
See the Position Description for additional information.
Conditions of Employment
• May be required to submit to annual TB and rubella screening.
• UNM will provide Hepatitis vaccination, candidate may decline vaccination through declination form or may provide record of vaccination from previous employer.
• Specialty licensure/certification may be required, as specified by the department.
• Successful candidate must submit to post-offer, pre-employment physical examination and medical history check.
• Must maintain certification status.
Minimum Qualifications
High school diploma or GED; at least 7 years of experience directly related to the duties and responsibilities specified.Certification/LicensureCurrent ACRP Certification as Clinical Research Coordinator or eligible for certification.
Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.
Preferred Qualifications
• Recent experience as a clinical research coordinator in oncology, hematology, or a related specialty.
• Recent experience with chart abstraction and IRB submissions.
• Experience with biospecimen processing and shipment.
• Experience designing and implementing research documentation systems and workflows.
Additional Requirements
Campus
Health Sciences Center (HSC) - Albuquerque, NM
Department
Pediatrics Hematology Oncology (997M)
Employment Type
Staff
Staff Type
Term - Full-Time
Term End Date
06/30/2027
Status
Exempt
Pay
Monthly: $3,841.07 - $5,148.00
Benefits Eligible
This is a benefits eligible position. The University of New Mexico provides a comprehensive package of benefits including medical, dental, vision, and life insurance. In addition, UNM offers educational benefits through the tuition remission and dependent education programs. See the Benefits home page for a more information.
ERB Statement
As a condition of employment, eligible employees working greater than .25 FTE as determined by the New Mexico Education Retirement Act must make mandatory retirement contributions. For more information, review the Benefits Eligibility at a Glance grid.
Background Check Required
Yes
For Best Consideration Date
10/6/2026
Eligible for Hiring Incentive
No
Eligible for Remote Work
No
Eligible for Remote Work Statement
Application Instructions
Only applications submitted throughthe official UNMJobs site will be accepted. If you are viewing this jobadvertisement on a 3rd party site, pleasevisit UNMJobs to submit an application.
A complete application will consist of a current resume, cover letter and references. Describe in your cover letter how you meet the preferred qualifications for the position. Include three references in your resume. The references must be former supervisors.Please complete the on-line application, include hours worked for each position.
Positions posted with a Staff Type of Regular or Term are eligible for the Veteran Preference Program. See the Veteran Preference Program webpage for additional details.
The University of New Mexico is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability, or any other protected class.
The University of New Mexico requires all regular staff positions successfully pass a pre-employment background check. This may include, but is not limited to, a criminal history background check, New Mexico Department of Health fingerprint screening, New Mexico Children, Youth, and Families Department fingerprint screening, verification of education credentials, and/or verification of prior employment. For more information about background checks, visit https://policy.unm.edu/university-policies/3000/3280.html. Refer to https://policy.unm.edu/university-policies/3000/3200.html for a definition of Regular Staff.
Requisition ID
req38124
Working Title
Clinical Research Supervisor
Position Grade
11
Position Summary
The University of New Mexico Health Sciences Center Pediatrics Department encompasses a statewide network of hospitals, clinics, and community-based services dedicated to advancing pediatric health through clinical excellence, education, and research. Within this system, the Pediatric Hematology/Oncology division provides the only comprehensive pediatric cancer and blood disorders program in New Mexico, offering a unique opportunity to support clinical, academic, research, and community-facing work.
The Clinical Research Supervisor coordinates, oversees, and quality-controls the execution of federally regulated clinical research studies, including multi-site pediatric oncology, hematology, hemophilia, and translational research trials. This position ensures full compliance with IRB/Human Research Review Committee (HRRC) requirements, Good Clinical Practice (GCP), federal/state regulations, institutional policies, and grant/contract parameters.
The supervisor provides day-to-day technical leadership, administrative oversight, and direct supervision of one staff member—a Research Technician 2—who supports data collection, biospecimen handling, and study coordination tasks. The role is responsible for operational strategy, workflow development, regulatory oversight, and ensuring accurate, reliable, and timely research data and biospecimen management.
The Clinical Research Supervisor collaborates closely with clinical investigators, IRB staff, national research organizations, study sponsors, and internal partners to ensure the smooth and efficient operation of all research, regulatory, and data collection activities. Duties include reviewing case report forms and source documents for completeness, accuracy, and compliance; initiating corrective actions; ensuring timely submission of research data; monitoring patient response to treatment as defined by protocol; and coordinating transmission of clinical data to national research organizations. This position is integral to sustaining high-quality research operations and advancing the mission of pediatric cancer and hematology research at UNM.
Duties and Responsibilities Include but are not limited to:
Supervision, Leadership & Operations
• Provides day-to-day technical leadership and direct administrative supervision to one Research Technician 2, including training, work allocation, productivity oversight, and performance evaluations.
• Plans, organizes, and oversees daily operations of the research unit, including protocol implementation, workflow design, systems development, and quality assurance.
• Develops operating goals and objectives and implements systems, procedures, and process improvements to enhance operational efficiency.
• Ensures appropriate scheduling and utilization of research resources, facilities, and equipment.
Regulatory & Compliance
• Ensures compliance with IRB/HRRC requirements, GCP guidelines, FDA regulations (as applicable), OSHA standards, and all federal, state, and institutional policies.
• Oversees development, submission, and maintenance of IRB applications, amendments, continuing reviews, deviations, and reportable events.
• Maintains regulatory documentation, study records, and essential documents in accordance with audit-ready standards.
Protocol Execution & Quality Control
• Supports investigators in study design, protocol development, and implementation.
• Oversees execution of multiple complex clinical research protocols, ensuring adherence to study timelines, visit windows, and data requirements. As well as consent/enrollment to both Therapeutic and Non-Therapeutic studies
• Develops, implements, and evaluates research and data collection methodologies, systems, and tools appropriate to pediatric oncology and hematology research.
• Reviews source data, case report forms, and eCRFs for accuracy, reliability, and protocol compliance; addresses deficiencies and initiates corrective action.
• Monitors and records patient responses to treatment as defined by protocol and coordinates data communication with investigators and sponsors.
Data & Specimen Management
• Coordinates data compilation, quality control, and preliminary analysis; ensures validity and accuracy prior to submission.
• Oversees and performs (as needed) the processing, tracking, and shipping of blood and human tissue samples in compliance with biosafety and shipping regulations.
• Ensures accurate transmission of clinical research data to national research organizations and sponsors.
Administrative & Financial
• Participates in budget development, cost tracking, and grant/contract administration.
• Ensures research billing compliance and alignment with coverage analyses for therapeutic and non-therapeutic trials.
• Documents operational activities, prepares reports, and supports audit and monitoring visits.
• Performs miscellaneous job-related duties as needed to support research growth and program demands.
See the Position Description for additional information.
Conditions of Employment
• May be required to submit to annual TB and rubella screening.
• UNM will provide Hepatitis vaccination, candidate may decline vaccination through declination form or may provide record of vaccination from previous employer.
• Specialty licensure/certification may be required, as specified by the department.
• Successful candidate must submit to post-offer, pre-employment physical examination and medical history check.
• Must maintain certification status.
Minimum Qualifications
High school diploma or GED; at least 7 years of experience directly related to the duties and responsibilities specified.Certification/LicensureCurrent ACRP Certification as Clinical Research Coordinator or eligible for certification.
Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.
Preferred Qualifications
• Recent experience as a clinical research coordinator in oncology, hematology, or a related specialty.
• Recent experience with chart abstraction and IRB submissions.
• Experience with biospecimen processing and shipment.
• Experience designing and implementing research documentation systems and workflows.
Additional Requirements
Campus
Health Sciences Center (HSC) - Albuquerque, NM
Department
Pediatrics Hematology Oncology (997M)
Employment Type
Staff
Staff Type
Term - Full-Time
Term End Date
06/30/2027
Status
Exempt
Pay
Monthly: $3,841.07 - $5,148.00
Benefits Eligible
This is a benefits eligible position. The University of New Mexico provides a comprehensive package of benefits including medical, dental, vision, and life insurance. In addition, UNM offers educational benefits through the tuition remission and dependent education programs. See the Benefits home page for a more information.
ERB Statement
As a condition of employment, eligible employees working greater than .25 FTE as determined by the New Mexico Education Retirement Act must make mandatory retirement contributions. For more information, review the Benefits Eligibility at a Glance grid.
Background Check Required
Yes
For Best Consideration Date
10/6/2026
Eligible for Hiring Incentive
No
Eligible for Remote Work
No
Eligible for Remote Work Statement
Application Instructions
Only applications submitted throughthe official UNMJobs site will be accepted. If you are viewing this jobadvertisement on a 3rd party site, pleasevisit UNMJobs to submit an application.
A complete application will consist of a current resume, cover letter and references. Describe in your cover letter how you meet the preferred qualifications for the position. Include three references in your resume. The references must be former supervisors.Please complete the on-line application, include hours worked for each position.
Positions posted with a Staff Type of Regular or Term are eligible for the Veteran Preference Program. See the Veteran Preference Program webpage for additional details.
The University of New Mexico is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability, or any other protected class.
The University of New Mexico requires all regular staff positions successfully pass a pre-employment background check. This may include, but is not limited to, a criminal history background check, New Mexico Department of Health fingerprint screening, New Mexico Children, Youth, and Families Department fingerprint screening, verification of education credentials, and/or verification of prior employment. For more information about background checks, visit https://policy.unm.edu/university-policies/3000/3280.html. Refer to https://policy.unm.edu/university-policies/3000/3200.html for a definition of Regular Staff.
Benefits
- Health insurance
- Dental insurance
Additional Details
- City
- Albuquerque
- State
- New Mexico
- Country
- US
Apply and matching require a free OVN account. Browse listings anytime without signing in.