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Duke Careers
Overview
Perform technical and clerical duties to support clinical research, including participant recruitment, data collection, and specimen processing. Ensure compliance with regulatory policies and assist in the preparation of IRB documentation and study reports.
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Compensation
$20 - $31 / HOUR
Posted
2 days ago
OneOncology
As the Research Nurse, you will screen, enroll, and follow study subjects, ensuring protocol compliance and monitoring. You will also be responsible for source documentation, recording adverse events, and dispensing investigational products.
Salary not listed
3 days ago
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
4 days ago
Evolution Research Group
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
9 days ago
The LPN or RN will assist in the conduct of clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing clinical procedures, maintaining accurate subject charts, and ensuring compliance with Good Clinical Practices.
The Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample collection. They are responsible for dispensing medications, documenting subject data, and maintaining a safe, compliant work environment according to study protocols.
American Oncology Network
Responsible for the implementation and management of clinical research studies, including patient coordination and protocol adherence. Tasks include managing study designs, ensuring data integrity, and maintaining regulatory compliance under the supervision of a Principal Investigator.
$20 - $35 / HOUR
11 days ago
Adams Clinical
The Laboratory Technician manages daily lab workflows, including specimen collection, processing, and shipping while ensuring compliance with clinical trial protocols. They also perform participant-facing clinical procedures such as phlebotomy, vital signs, and ECGs to support study visit flow.
$24 - $27 / HOUR
14 days ago
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
ICON plc
The Clinical Research Nurse provides direct clinical care to research participants and administers investigational products while monitoring safety. They also coordinate study procedures, ensure protocol compliance, and maintain accurate documentation of research data.
17 days ago
DM CLINICAL RESEARCH GROUP
The Unblinded Clinical Research Coordinator II will be responsible for dispensing Investigational Products as part of clinical research trials and ensuring compliance with study-specific blinding plans. They will also supervise medication records, assist in training new team members, and maintain documentation of IP accountability.
24 days ago
The Unblinded Clinical Research Coordinator II will be responsible for dispensing Investigational Products as part of clinical research trials and ensuring compliance with study-specific blinding plans. They will also supervise medication records, assist in training new team members, and interact with various stakeholders to ensure protocol adherence.
WEP Clinical
Provide high-quality nursing care and administer investigational products to patients within their homes. Ensure strict adherence to study protocols, conduct medical tests, and maintain accurate documentation for clinical research.
$55 / HOUR
28 days ago
ALX Oncology Inc.
Supports clinical operations by managing the Trial Master File (TMF), coordinating site activation, and tracking study documents. Collaborates with CROs and internal teams to ensure regulatory compliance and efficient trial execution.
$100,000 - $120,000 / YEAR
29 days ago
Washington University in St. Louis
This role coordinates and implements research studies, managing data collection while ensuring continuity of patient care and protection of human subjects under the Principal Investigator's guidance. Responsibilities include providing direct patient care, administering study interventions and medications, processing specimens, and collaborating with multidisciplinary teams and sponsors.
$56,200 - $96,100 / YEAR
Coordinates and implements cardiology research studies, including data collection, patient screening, and enrollment. Manages protocol requirements, regulatory submissions to the IRB, and the administration of investigational products.
1 month ago
The Clinical Research Pharmacist oversees the pharmacy components of clinical trials, ensuring regulatory compliance and quality control for investigational products. They provide clinical support, patient education, and supervision to pharmacy staff while coordinating between research and pharmacy departments.
Profound Research
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols and regulations. They also mentor staff and ensure accurate documentation and reporting of adverse events.
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Nurse manages all aspects of Phase I-IV oncology clinical trials, including patient care, protocol execution, and data collection. They collaborate with Principal Investigators to ensure participant safety, regulatory compliance, and accurate reporting of clinical outcomes.
$62,000 - $95,094 / YEAR
University of Pennsylvania
The Clinical Research Nurse manages Phase I-IV oncology clinical trials, ensuring participant safety and protocol compliance in collaboration with Principal Investigators. Responsibilities include coordinating patient care, administering study treatments, and maintaining accurate clinical trial data.
