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IQVIA
Overview
The intern supports the preparation, documentation, and management of investigational products for clinical trials under pharmacist supervision. Key duties include managing drug accountability logs, dispensing medications per protocol, and ensuring regulatory compliance with FDA and IRB standards.
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Compensation
$33,000 - $82,600 / YEAR
Posted
2 days ago
Mass General Brigham
Prepares sterile and non-sterile products in adherence to USP and hospital policies while managing investigational prescriptions via the CTP system. Responsible for inventory management, temperature monitoring, and coordinating with study teams and sponsors for clinical trials.
$21 - $30 / HOUR
Toledo Clinic
The Research Pharmacy Technician manages investigational drug services, including sterile compounding of hazardous and non-hazardous drugs in compliance with USP 797 and 800 guidelines. They also maintain drug inventory, ensure product accountability, and support the research pharmacist with administrative and clinical research tasks.
Salary not listed
8 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
University of Texas Medical Branch (UTMB)
The coordinator obtains human subject data according to study protocols and performs administrative duties to support clinical research. Key tasks include recruiting participants, managing regulatory documentation, and processing laboratory specimens.
16 days ago
ICON plc
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 entry and site documentation.
17 days ago
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing data integrity, and overseeing drug accountability.
MyMichigan Health
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and act as a liaison between investigators, sponsors, and participants.
22 days ago
IU Health
The technician manages investigational drug products, including receiving, documenting inventory, and performing sterile and non-sterile compounding. They also monitor storage environments and assist with auditing records to ensure regulatory compliance.
26 days ago
K2 Staffing LLC
The Pharmacy Specialist manages the receipt, storage, and dispensing of study drugs while ensuring strict compliance with FDA regulations and study protocols. They also develop training programs for clinic staff and coordinate study close-out procedures with sponsors.
1 month ago
Allina Health
This role involves coordinating high-quality care for patients in clinical research studies by ensuring standards are met, educating participants, and collaborating across disciplines to support safe and effective study outcomes. Key duties include ensuring patient care aligns with the research protocol, performing safety monitoring, conducting patient evaluations, and assisting the investigator with protocol-specific tasks like dose modifications.
$37 - $51 / HOUR
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing site documentation, and overseeing drug accountability throughout the clinical trial process.
$91,336 - $114,170 / YEAR
Mens Health Foundation
The Clinical Research Coordinator will manage the planning and implementation of clinical research projects, including participant recruitment, study procedure execution, and data collection. They will ensure compliance with study protocols, GCP guidelines, and regulatory requirements while maintaining accurate source documentation.
$25 - $34 / HOUR
Worldwide Clinical Trials
The PRN Pharmacist oversees daily pharmacy operations, ensuring study medications are managed, dosed, and documented according to protocol and regulatory requirements. They also supervise pharmacy technicians and coordinate with site leadership to maintain compliance with FDA and DEA standards.
CC DERMATOLOGY MSO LLC
The role involves managing drug accountability, dispensing blinded study medications, and maintaining accurate regulatory documentation. Additionally, the coordinator will assist with participant visits and ensure adherence to study protocols and Good Clinical Practice guidelines.
MAPMG
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required procedures. They also ensure regulatory compliance, maintain accurate study documentation, and monitor patient outcomes throughout the study lifecycle.
$79,370 - $99,213 / YEAR
The Pharmacy Specialist assists in drug management and compliance, ensuring proper handling and documentation of drug products. They also support quality assurance and training for clinic staff interacting with the pharmacy.
2 months ago
Northwell
The coordinator is responsible for managing designated research studies, overseeing subject recruitment, implementing study procedures, and ensuring accurate data collection and specimen handling according to protocol. This role involves scheduling subjects, collaborating with healthcare providers, administering assessments, and maintaining drug accountability logs.
$64,350 - $86,060 / YEAR
Astera
The Clinical Research Coordinator will provide overall coordination for study-related activities for patients in cancer research studies, ensuring activities adhere to local and federal regulations and sponsor policies. Responsibilities include assisting with IRB submissions, maintaining regulatory documents, coordinating patient tests and visits, and entering research data into a centralized database.
3 months ago
Flourish Research
The Pharmacy Technician supports clinical research sites by handling pharmaceutical preparation, distribution, and record keeping for study participants according to procedures. This role is crucial for supporting clinical staff and ensuring smooth, compliant site operations.
$29 - $41 / HOUR
