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Headlands Research
Overview
The Pharmacy Technician is responsible for the safe handling, preparation, and dispensing of investigational products in accordance with study protocols and GCP regulations. They also manage pharmacy documentation, maintain inventory logs, and provide administrative support for clinical trials.
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Compensation
$22 - $26 / HOUR
Posted
4 days ago
University of Iowa
Provide direct nursing care and administer investigational treatments for Phase I-IV clinical trials. Collaborate with medical staff to ensure participant safety and strict adherence to research protocols.
Salary not listed
5 days ago
The Laboratory Technician performs specimen collection, processing, documentation, and shipment for clinical trials in compliance with GCP and study protocols, while also assisting with vital signs, ECGs, and maintaining laboratory equipment and cleanliness. Responsibilities also include accurate data recording, resolving data queries, monitoring lab inventory, and supporting study preparation activities.
7 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.
10 days ago
The Research Nurse provides direct clinical care to subjects in Phase I-IV diabetes trials, focusing on safety and protocol compliance. Key duties include IV placement, administering research medications, and detailed data collection following Good Documentation Practices.
$55 - $60 / HOUR
University of Pennsylvania Perelman School of Medicine
Manage Phase I-IV oncology clinical trials, including participant care, medication administration, and data collection. Collaborate with Principal Investigators to design and execute studies while ensuring compliance with regulatory standards.
$63,085 - $98,113 / YEAR
11 days ago
Flourish Research
The Clinical Research Assistant supports investigators in executing Phase I-IV clinical trials following SOP, FDA, and GCP guidelines. Key duties include recruiting patients, obtaining informed consent, collecting data, and performing clinical tasks like vital signs and ECGs.
$20 - $22 / HOUR
14 days ago
The coordinator executes protocol-specified patient visits and procedures while ensuring all study data is documented according to GCP and FDA guidelines. They are also responsible for ethical subject recruitment, obtaining informed consent, and managing trial materials.
$25 - $28 / HOUR
15 days ago
Georgetown University
Manage and coordinate a subset of clinical trials focusing on neuroimmunology and neuromuscular diseases, ensuring strict protocol adherence during patient visits. Responsible for regulatory maintenance, accurate data entry in OnCore/CTMS, and maintaining constant communication with patients and sponsors.
$44,022 - $73,407 / YEAR
University of California, Irvine
Coordinate and manage Phase I-IV cancer-related clinical trials, ensuring adherence to GCP, SOPs, and university policies. Act as a liaison between sponsors, regulatory agencies, and the research team while managing patient recruitment and data collection.
16 days ago
CenExel
The role is responsible for recruiting clinical trial participants via telephone and managing recruitment programs to increase referrals. Key duties include performing initial screenings, scheduling appointments in Clinical Conductor, and maintaining professional relationships with participants.
Hoag
The Clinical Research Coordinator RN manages all aspects of FDA-regulated clinical trials, from protocol review and subject recruitment to data collection and regulatory maintenance. They work closely with study physicians to ensure the accurate execution of Phase I-IV trials and maintain compliance with Good Clinical Practices.
$49 - $76 / HOUR
1 month ago
The Clinical Research Coordinator executes Phase I-IV clinical trials by obtaining informed consent and performing protocol procedures. Responsibilities include specimen collection, e-source documentation, and coordinating with study sponsors and CROs.
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and assisting with clinical assessments. They are also responsible for data entry, query resolution, and facilitating study monitoring visits while adhering to strict research protocols.
$20 - $21 / HOUR
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
The Clinical Research RN is responsible for implementing daily clinical study activities and serving as a liaison between the investigative site and the sponsor. They must accurately document all research information, monitor study participants, and ensure adherence to clinical protocols and regulatory standards.
The Lab Technician will perform laboratory procedures, process clinical samples according to protocol, and maintain accurate inventory and harvest logs. They are also responsible for monitoring storage temperatures and ensuring all study materials are properly labeled and stored.
The Nurse Practitioner provides primary care and assists in the evaluation and treatment of research participants. They ensure adherence to clinical protocols and maintain the integrity of data generated during investigations.
2 months ago
The Registered Nurse oversees daily clinical study activities, including monitoring patient vitals and administering investigational medication per protocol. They serve as a liaison between the investigative site and the sponsor while ensuring accurate documentation and compliance with study requirements.
$39 - $43 / HOUR
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, preparing visit materials, and assisting with clinical assessments. They are also responsible for data entry, inventory management, and facilitating study monitoring visits.
$20 / HOUR
