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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
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
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
15 days ago
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.
$20 - $22 / HOUR
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
Flourish Research
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
The Clinical Research Coordinator III is responsible for managing all aspects of complex clinical research trials, including drug, device, and biologic studies, while collaborating with physicians and stakeholders. Key duties involve conducting protocol review, administering informed consent, recruiting subjects, ensuring accurate data collection, completing CRFs, and overseeing adverse event reporting and subject follow-up.
$39 - $59 / HOUR
Roche
The Medical Science Liaison is responsible for providing clinical and scientific information regarding disease states and Genentech medicines in the MASH pipeline to healthcare providers and thought leaders within their region. Key activities include driving clinical trial recruitment, gathering competitive intelligence, supporting congress engagement, and sharing rich customer insights across the organization.
$161,280 - $299,520 / YEAR
3 months ago
