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Systimmune
Overview
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
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Compensation
$90,000 - $130,000 / YEAR
Posted
9 days ago
University of Chicago
Coordinates and conducts complex clinical research studies while ensuring compliance with federal and institutional regulations. Acts as a key liaison between investigators, sponsors, and university departments to manage study documentation and operational workflows.
$60,000 - $75,000 / YEAR
17 days ago
Tufts Medicine
This role involves assisting the Principal Investigator in planning and implementing clinical research studies, including participant recruitment, screening, and follow-up activities. Responsibilities also cover maintaining regulatory compliance, managing study documentation, performing basic lab activities, and coordinating data collection and query resolution.
$47,924 - $59,895 / YEAR
29 days ago
AstraZeneca
Field Clinical Advisors are crucial for the successful execution of cell therapy clinical trials by driving recruitment, retention, and safety management while generating early insights. They focus on clinical study protocol expertise, educating sites, optimizing the patient journey, and engaging with the cell therapy pipeline.
$197,000 - $295,000 / YEAR
1 month ago
EvergreenHealth
Coordinates the operations of neuroscience research studies, managing patient records, databases, and case report forms. Responsibilities include recruiting subjects, ensuring protocol adherence, and handling IRB submissions and specimen shipping.
Salary not listed
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
Cell Therapy Field Clinical Advisors are crucial for the successful execution of clinical trials by driving recruitment, retention, and safety management, while also providing early insight generation. They focus on clinical study protocol expertise, educating sites, optimizing the patient journey, and engaging with the cell therapy pipeline.
IQVIA
The Senior CRA is responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. They conduct site visits, support subject recruitment, and maintain essential study documentation to ensure data integrity.
$87,200 - $169,300 / YEAR
MDxHealth
The Clinical Research Associate assists the Clinical Affairs Team in managing clinical research studies and acts as a liaison between the lab and study accounts. Responsibilities include monitoring study sites, managing specimen tracking, and ensuring compliance with SOPs.
$64,500 - $75,000 / YEAR
2 months ago
This role assists the Principal Investigator in planning and implementing clinical research studies, primarily by managing participant recruitment, conducting eligibility assessments, and obtaining informed consent. Essential duties also involve completing follow-up activities, abstracting source documents, completing Case Report Forms, and ensuring data quality and entry.
$44,779 - $55,978 / YEAR
ImmunityBio, Inc.
The Senior CRA, Field Monitor will participate in clinical research teams to ensure efficient study conduct by providing training, protocol interpretation, document collection/review, and overall clinical trial support. Essential functions include developing training materials, serving as a Subject Matter Expert, overseeing document collection, reviewing data, and training site personnel and vendors on study requirements.
$62 - $67 / HOUR
University of Texas at Austin
The Clinical Research Associate I will manage and oversee the day-to-day coordination and operations of assigned clinical research projects, focusing significantly on recruitment, enrollment, and research activities within the Department of Psychiatry. Key duties involve assisting in the planning, execution, and monitoring of clinical trials to ensure strict compliance with regulatory requirements and study protocols, including site management and data integrity.
$40,000 / YEAR
3 months ago
Cooper University Hospital
The Oncology Research Coordinator oversees clinical studies, managing quality of life and specimen trials while coordinating patient recruitment and informed consent. They are responsible for maintaining study documentation, ensuring GCP compliance, and collaborating with multidisciplinary cancer teams.
$28 - $46 / HOUR
