Senior Level Assistant Clinical Research Associate Jobs
Senior level assistant clinical research associate jobs place experienced professionals in charge of trial oversight, protocol adherence, and the site teams and study timelines that keep complex research on track. Roles are concentrated in Healthcare & Medical Services, Biotechnology & Pharmaceuticals, and Education, with a mix of on-site, hybrid, and remote positions available, and employers like Jobot, Guthrie, and NS Pharma hiring at this level now.
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Showing 5 of 21+ Senior Level Assistant Clinical Research Associate jobs
Clinical Research Supervisor
Requisition ID req38466
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.
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/Licensure Current 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
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.
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 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 11/17/2026
Eligible for Hiring Incentive
Eligible for Remote Work No
Eligible for Remote Work Statement This position is not eligible for Remote work.
Application Instructions
Only applications submitted through the official UNMJobs site will be accepted. If you are viewing this job advertisement on a 3rd party site, please visit 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. Please provide contact information for 3 professional references, preferably former supervisors. Please complete the online application, including 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 to 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.
Clinical Research Supervisor
Requisition ID req38466
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.
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/Licensure Current 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
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.
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 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 11/17/2026
Eligible for Hiring Incentive
Eligible for Remote Work No
Eligible for Remote Work Statement This position is not eligible for Remote work.
Application Instructions
Only applications submitted through the official UNMJobs site will be accepted. If you are viewing this job advertisement on a 3rd party site, please visit 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. Please provide contact information for 3 professional references, preferably former supervisors. Please complete the online application, including 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 to 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.
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Senior Level Assistant Clinical Research Associate Jobs: Frequently Asked Questions
How do I get a senior level assistant clinical research associate job?
Employers at this level expect candidates who can independently manage site relationships, identify and resolve monitoring issues before they escalate, and train or guide junior staff. Demonstrating ownership of previous study deliverables, familiarity with ICH-GCP guidelines, and experience across multiple therapeutic areas signals readiness for senior responsibility. Tailoring your application to show scope of oversight and cross-functional collaboration gives you a clear edge.
Which companies hire senior level assistant clinical research associates?
Companies hiring senior level assistant clinical research associates right now include Jobot, Guthrie, and NS Pharma, based on current listings on Migrate Mate as of November 2026. Hiring at this level is concentrated among contract research organizations, large pharmaceutical sponsors, and medical device companies running multi-site or global clinical programs.
Are there remote senior level assistant clinical research associate jobs?
Yes, though many roles still require periodic site visits depending on study phase and sponsor requirements. About 43% of senior level assistant clinical research associate openings are remote or hybrid as of November 2026, reflecting the industry's broader adoption of risk-based monitoring models that allow more off-site oversight work.
What makes an assistant clinical research associate role senior level?
Senior level roles are defined by independent site management, accountability for data quality across a portfolio of sites, and responsibility for mentoring junior associates. Where mid-level positions involve executing monitoring tasks under guidance, senior roles require setting expectations for site teams, escalating protocol deviations with recommended resolutions, and contributing to process improvements within the monitoring function.
Which industries hire the most senior level assistant clinical research associates?
Senior level assistant clinical research associate roles concentrate in Healthcare & Medical Services, Biotechnology & Pharmaceuticals, and Education, based on current listings on Migrate Mate as of November 2026. These sectors drive demand because they run the largest volumes of regulated clinical trials and need experienced monitors who can operate with minimal oversight across complex, multi-site studies.