Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
4 C Medical Technologies
Overview
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
Quick view →
Compensation
$75,000 - $95,000 / YEAR
Posted
6 days ago
Terumo
The Clinical Research Coordinator provides administrative and operational support to the Clinical Research and Operations department to ensure adherence to study plans and regulatory standards. Responsibilities include managing study documentation, maintaining the electronic trial master file, and coordinating with clinical sites and vendors.
$44,900 - $61,710 / YEAR
7 days ago
AstraZeneca
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.
$112,154 - $168,232 / YEAR
11 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.
RLS Radiopharmacies
The Pharmacy Technician compounds, dispenses, and packages radiopharmaceuticals while performing quality control and leukocyte labeling. They are also responsible for maintaining cleanroom disinfection, stocking sterile supplies, and ensuring regulatory documentation compliance.
Salary not listed
14 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.
22 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
You will be responsible for the preparation, initiation, monitoring, and closure of clinical study centers while ensuring compliance with international guidelines and local regulations. You will work in collaboration with the local study team to ensure quality and quantity commitments are met in a timely manner.
$101,948 - $152,922 / YEAR
2 months ago
Northwestern Memorial Healthcare
The Senior Cellular Therapy Scientist is responsible for the manufacturing of cell and gene therapy products, ensuring compliance with regulatory standards. They also provide technical oversight and assist in the day-to-day operations of the laboratory.
$36 - $49 / HOUR
