Clinical Research Associate Jobs in New Mexico, United States

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

We are seeking Clinical Research Associates (CRAs) with oncology monitoring experience to work remotely across California, Nevada, Idaho, New Mexico, and Colorado. The role, titled Sr CRA I / CRA 2 – FSP – Oncology, involves comprehensive site monitoring and management for clinical studies under Fortrea and sponsor SOPs.

We are seeking an experienced Oncology Clinical Research Associate (CRA) to lead and support our full-service outsourcing team. The role focuses on site monitoring, data integrity, SAE reporting, and regulatory compliance for CAR‑T trials.

Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments.

Clinical Research Coordinator II at Cincinnati Children’s Hospital Medical Center’s South Campus team. The role coordinates pediatric clinical studies, preparing protocols, managing informed consent, and ensuring regulatory compliance with GCP and IRB standards.

Clinical Research Team at IQVIA coordinates multi-site studies to advance medical innovations. The Clinical Research Coordinator manages study operations, conducts patient visits and procedures, ensures data integrity in EDC systems, and supports recruitment and regulatory compliance.

Dedicated Clinical Research Assistant supporting Phase I–III gynecologic oncology trials in Albuquerque. Coordinates study start‑up, regulatory docs, IRB submissions, and patient scheduling.

Clinical Research Director leading SWWO's high-performance research program in Albuquerque. Oversees daily operations, ensuring compliance with FDA, GCP, ICH, and IRB standards.

IQVIA Clinical Research team in Albuquerque, NM focuses on advancing patient outcomes through rigorous clinical studies. As a Clinical Research Coordinator, you will manage study operations, conduct patient visits, and ensure data integrity in EDC systems.

DM Clinical Research team manages investigational product dispensing for clinical trials. The Coordinator compounds and dispenses IP, manages study IP inventory, conducts audits, and trains new staff while ensuring compliance with blinding plans.

Per Diem Mobile Research Nurse on Science 37’s Nursing Solutions Group, a team that designs and delivers mobile clinical nurse services for decentralized clinical trials. The role provides bedside care to study participants at home, collaborates with lead nurses and research teams, and ensures compliance with Good Clinical Practice and federal regulations.

Science 37’s Nursing Solutions Group delivers mobile clinical nurse services to clinical trial participants. The Mobile Research Nurse provides bedside care at participants’ homes, collaborates with lead nurses and study teams, and ensures compliance with GCP and SOPs.

Rehabilitation Research Division at Memorial Hermann leads clinical research on spinal cord injury rehabilitation. The Director shapes strategic research plans, oversees the TIRR Research Council, advises the CEO, and drives grant acquisition and collaborative partnerships.

Coordinates and assists with the implementation of multiple clinical research studies. Candidates with Oncology Regulatory clinical research experience highly preferred.

Study Manager I at DM Clinical Research Group in Albuquerque, NM. The role ensures quality clinical research at investigative sites, overseeing protocol adherence, training, data quality, and patient consent. Responsibilities include managing site staff, coordinating sponsor visits, and reporting safety events.

Site Manager at DM Clinical Research Group leads the clinical research team in Albuquerque, ensuring FDA, ICH/GCP compliance and high‑quality data delivery. The role supervises site staff, coordinates training, manages protocol adherence, and drives enrollment targets while maintaining rigorous data quality.

Site Manager oversees clinical research sites, ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP standards. Responsible for training, supervising staff, and maintaining study documentation.

IQVIA, a global leader in clinical research and healthcare intelligence, seeks an Inside Sales Representative for its Diabetes portfolio. The role focuses on promoting Endocrinology/Diabetes products to healthcare professionals, achieving sales forecasts, and building relationships with physicians.

Oncology Regional Medical Scientific Director (RMSD) at Merck leads scientific exchange, clinical research support, and congress engagement for genitourinary oncology across Colorado, Arizona, New Mexico, Utah, and Kansas. The role builds relationships with scientific leaders, provides balanced medical information, and identifies enrollment barriers for clinical trials while serving as a mentor for field medical team members.

This role engages with healthcare professionals to provide scientific support and build relationships in oncology. The MSL will collaborate with key opinion leaders, facilitate educational programs, and support clinical research initiatives.