Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
MedWiz of New Jersey LLC
Overview
The Regulatory Compliance Technician provides support to ensure compliance with pharmacy laws and regulations. This includes maintaining licenses, tracking compliance documentation, and preparing for audits.
Quick view →
Compensation
Salary not listed
Posted
8 days ago
Evolution Research Group
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They are responsible for ensuring protocol adherence, managing subject recruitment, and maintaining accurate regulatory documentation under the direction of the Principal Investigator.
9 days ago
Sarasota Memorial Health Care System
Responsible for the timely and accurate administration of regulatory compliance for clinical research, including processing Human Research Protection Program and IRB documentation. The role involves informing leadership and staff regarding the regulatory status of clinical trials.
11 days ago
Duke Careers
The Regulatory Coordinator will manage regulatory operations for complex oncology studies, ensuring compliance and audit readiness. This includes preparing and submitting necessary documentation and coordinating study management activities.
$59,829 - $99,960 / YEAR
15 days ago
The US Oncology Network
Responsible for managing research regulatory and administrative activities for clinical trials, including site qualification and document management. Collaborates with investigators and central operations to ensure compliance with SOPs, GCP, and federal regulations.
24 days ago
Medical University of South Carolina
The coordinator manages pre-award grant processes, including budget development and proposal submission. They also ensure regulatory compliance by managing IRB documentation and adhering to FDA and GCP requirements.
$37,200 - $59,500 / YEAR
1 month ago
Nationwide Children's Hospital
Assists with administrative components to ensure regulatory compliance for clinical research projects, including maintaining study binders and files. Prepares and submits IRB documents while ensuring accuracy across regulatory and grant systems.
Assists with administrative components to ensure regulatory compliance for clinical research projects. Responsibilities include maintaining study binders, submitting IRB documents, and collecting investigator credentials.
WakeMed Health & Hospitals
Performs routine and specialized laboratory tests to assist in disease diagnosis and treatment while maintaining laboratory equipment and supplies. Trains new staff and assumes responsibility for specific laboratory projects such as quality control and regulatory compliance.
Performs routine and specialized laboratory tests while evaluating and reporting patient results using independent judgment. Assists in the maintenance of laboratory equipment, quality control procedures, and the training of new staff members.
Pharmaron
The Clinical Regulatory Associate manages essential clinical trial documentation, IRB submissions, and study start-up activities. They ensure compliance with GCP, GLP, and internal procedures while supporting monitoring visits and study closeout activities.
$50,000 - $54,000 / YEAR
Indiana Organ Procurement Organizat
The Organ Regulatory Compliance Coordinator is responsible for maintaining and reporting accurate procurement data to ensure compliance with regulatory requirements. This role involves conducting quality assurance reviews, managing patient files, and coordinating donation-related outcomes with transplant centers and external partners.
Ohio County Healthcare
The APRN will provide quality patient care, perform clinical assessments, and prescribe medications in collaboration with physicians. They are also responsible for maintaining accurate documentation and communicating effectively with patients and their families.
HonorHealth
The coordinator facilitates regulatory affairs for clinical research, ensuring compliance with FDA, ICH, and IRB standards. They manage study protocols from startup through closure, including document preparation and regulatory correspondence.
CenExel
The Clinical Research Coordinator assists with the coordination of clinical trials from initiation to completion, ensuring strict adherence to protocols and regulatory guidelines. Responsibilities include managing research data, performing safety assessments, and maintaining quality and compliance throughout the study process.
$28 - $35 / HOUR
UHS
The pharmacist is responsible for the daily operations of the pharmacy, including the management and documentation of controlled substances. They also assist in tracking medication errors and adverse drug reactions to implement procedures that minimize future risks.
QPS, LLC
The Site Systems Coordinator serves as an operational liaison between study system configuration and clinical execution to ensure eSource builds align with site workflows. They are responsible for reviewing methods, edit checks, and processing pathways while identifying operational risks and maintaining audit readiness.
The Christ Hospital Health Network
The Regulatory Assistant supports the regulatory team by ensuring all tasks and documents are accurate, complete, and processed efficiently. They promote quality and speed in the Lindner Research-Oncology regulatory process to facilitate timely project start-ups.
The Clinical Research Coordinator manages patient involvement and study data in strict adherence to ICH and GCP guidelines. They also assist with regulatory duties, safety assessments, and provide support to the Clinical Trial Manager.
Cedars-Sinai
The Regulatory Coordinator prepares and submits clinical trial protocols and supporting documentation to various regulatory bodies and committees. They ensure ongoing compliance with federal and local regulations, including FDA and IRB requirements, while maintaining accurate research files.
$34 - $58 / HOUR
