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University of Massachusetts Medical SchoolNew
Overview
The Research Associate provides operational support to the laboratory, performing research experiments focused on microbiota-metabolite-immune system crosstalk in the intestines using advanced techniques like flow cytometry, sequencing, and metabolomics. Responsibilities scale with rank, ranging from performing basic experiments and maintaining records to independently designing complex experiments, managing lab operations, and contributing to grant and manuscript writing.
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Compensation
Salary not listed
Posted
New
Arc Institute
Perform molecular and cellular experiments to identify pathways driving neurodegenerative diseases using CRISPR and functional assays. Collaborate with scientists to conduct large-scale genetic screenings using stem cell-derived brain models.
$75,900 / YEAR
2 days ago
Cedars-Sinai
The Research Associate II performs complex laboratory tasks and experimental protocols to support cancer research focusing on the immune system. Responsibilities include maintaining lab equipment, documenting results, and assisting in the preparation of data for scholarly publications.
$24 - $36 / HOUR
3 days ago
University of Massachusetts Medical School
The Research Associate III independently performs complex laboratory experiments and manages general lab operations, including personnel and supplies. They are responsible for analyzing data, drafting manuscripts, and ensuring compliance with safety and regulatory protocols.
ICON plc
Serve as the primary contact between investigational sites and sponsors while conducting various site visits including initiation and close-out. Ensure site compliance with ICH-GCP and regulations while managing data queries and patient safety reporting.
4 days ago
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data quality and site documentation.
$91,336 - $114,170 / YEAR
PSI CRO
The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while ensuring data integrity and compliance.
5 days ago
Caris Life Sciences
Perform a wide range of molecular biology techniques including nucleic acid extraction, sequencing, and protein analysis. Responsible for laboratory maintenance, inventory management, and training junior technical staff.
9 days ago
Coordinate and implement complex clinical research studies focusing on behavioral health interventions for LGBTQ+ communities of color. Responsibilities include data collection, IRB submission assistance, participant prescreening, and ensuring compliance with federal and local guidelines.
Thermo Fisher Scientific
The CRA II is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting on-site and remote visits, managing essential documentation, and maintaining relationships with clinical sites.
$80,000 - $125,000 / YEAR
10 days ago
Fortrea
Responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and maintenance of study files. Ensures the protection of study patients and the integrity of data submitted via Case Report Forms.
$105,000 - $118,000 / YEAR
12 days ago
University of Texas Medical Branch (UTMB)
Performs routine and non-routine research experiments and assists with laboratory maintenance and safety compliance. Responsibilities include preparing biological assays, analyzing data, and managing lab inventory under the supervision of a Principal Investigator.
Perform routine and non-routine research experiments and biological assays under general supervision. Maintain laboratory equipment, inventory, and ensure compliance with animal and environmental safety standards.
15 days ago
Corcept Therapeutics
The CRA II monitors clinical study activities to ensure adherence to GCP, SOPs, and study protocols. Responsibilities include supervising site preparation, managing clinical vendors, and drafting essential study documents like protocols and informed consent forms.
$129,400 - $152,300 / YEAR
16 days ago
The role involves planning and directing moderately complex research experiments and overseeing quality control measures. Responsibilities include analyzing data, maintaining detailed records, and managing laboratory equipment and inventory.
$55,000 / YEAR
17 days ago
Conducts non-routine research experiments and manages quality control measures for assigned projects. Responsible for data collection, analysis, and the maintenance and calibration of laboratory equipment.
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
19 days ago
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with site staff and investigators while performing data review to maintain high-quality clinical documentation.
IQVIA
Support antibody discovery and library pipeline activities through hands-on molecular biology laboratory work. Execute analytical procedures, maintain compliant records, and assist with process improvements to ensure high-quality data.
$51,800 - $108,000 / YEAR
23 days ago
