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AstraZeneca
Overview
The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and local regulations. They act as the primary contact for study sites, managing data quality, drug accountability, and reporting of serious adverse events.
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Compensation
$112,154 - $168,232 / YEAR
Posted
2 days ago
Thermo Fisher Scientific
Perform technical procedures such as phlebotomy, ECGs, and vital signs monitoring for Phase I clinical trials. Interact with study subjects and conduct safety monitoring to ensure successful data collection.
$17 / HOUR
5 days ago
The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and local regulations. They act as the primary contact for study sites, managing data quality, patient recruitment progress, and regulatory documentation.
PerkinElmer
Supports records management and document digitization activities within the Quality Team as part of a Laboratory Modernization Program. Responsibilities include scanning, indexing, and maintaining electronic laboratory records to ensure data integrity and inspection readiness.
Salary not listed
IQVIA
The technician will be responsible for entering concomitant medications, preparing investigational products according to protocol, and compounding IV and oral agents adhering to USP standards. Key duties also involve managing drug inventory documentation and providing administrative support for audits and SOP development.
$33,000 - $82,600 / YEAR
6 days ago
Baylor Scott & White Health
Coordinates the acceptance, preservation, and distribution of human islet tissues while developing quality control protocols and SOPs. Supervises lab activities and ensures compliance with FDA regulations for a GMP facility.
9 days ago
Altos Labs
Execute research and development experiments using human iPSC models to support cellular rejuvenation and aging studies. Develop innovative laboratory techniques and provide technical mentorship and training for specialized in vitro culture workflows.
$109,200 - $140,000 / YEAR
12 days ago
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for study sites, driving performance, resolving issues, and ensuring data quality through monitoring visits and source data review.
13 days ago
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for sites, driving performance, resolving study-related issues, and managing study supplies.
Cleveland Diagnostics
The Laboratory Assistant supports CLIA lab operations by receiving, preparing, and accessioning biological specimens into the LIS. They are also responsible for routine instrument maintenance, inventory management, and ensuring compliance with documentation and safety policies.
$24 - $26 / HOUR
15 days ago
The Senior Clinical Research Associate is locally responsible for study delivery at allocated sites, acting as the main contact for monitoring study conduct to ensure compliance with guidelines like ICH-GCP. Responsibilities include performing site visits, driving site performance, resolving study issues proactively, and managing site training and enrollment milestones.
24 days ago
The IDS Pharmacist ensures protocol integrity, patient safety, and regulatory compliance for Phase 1 Oncology trials. Responsibilities include medication dispensing, compounding, inventory management, and supervising IDS technicians.
$57,700 - $209,800 / YEAR
26 days ago
BioIVT
This position is responsible for efficiently and accurately performing blood collection and non-blood collection from donors while ensuring strict compliance with various regulatory guidelines, including EHS, GDP, GLP, GMP, and GCP. Essential duties involve consenting donors, performing pre-donation screening, collecting specimens according to SOPs, maintaining records, and assisting with facility maintenance and sample processing for shipment.
$18 - $22 / HOUR
1 month ago
Planned Systems International, Inc.
The phlebotomist is responsible for screening and registering blood donors, conducting health histories, and performing whole blood collection and apheresis procedures. They must also ensure accurate documentation, specimen handling, and equipment maintenance while monitoring donors for adverse reactions.
Keck Medicine of USC
The Clinical Laboratory Scientist performs specialized biochemical, hematological, and microbiological analyses to ensure accurate and timely patient test results. They are also responsible for maintaining laboratory equipment, documenting quality control, and assisting in the training of personnel.
$46 - $76 / HOUR
The Clinical Laboratory Scientist performs specialized biochemical, hematological, and microbiological analyses to ensure accurate and timely patient test results. They are also responsible for maintaining laboratory equipment, monitoring inventory, and adhering to strict safety and quality control protocols.
University of Southern California
The Clinical Laboratory Scientist performs specialized biochemical, hematological, and microbiological analyses to ensure accurate and timely patient test results. They are also responsible for maintaining laboratory equipment, managing inventory, and adhering to strict safety and quality assurance protocols.
Octapharma
The Phlebotomist 3 is responsible for performing venipunctures and operating automated plasmapheresis machines while ensuring compliance with safety and quality regulations. They also oversee donor flow, mentor team members, and maintain accurate documentation and work area cleanliness.
University of Chicago
The Clinical Research Coordinator 1 performs routine assignments related to the documentation and reporting of clinical studies and supports decisions impacting clinical research. Responsibilities include environmental monitoring, equipment maintenance, compliance with regulatory policies, and preparation of cellular products.
$50,000 - $65,000 / YEAR
2 months ago
