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Glaukos
Overview
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
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Compensation
$73,600 - $85,000 / YEAR
Posted
10 days ago
CenExel
The Clinical Research RN I oversees daily clinical study activities and serves as a liaison between the investigative site and the sponsor. Responsibilities include providing nursing care to participants, executing research protocols, and ensuring ethical documentation of all study data.
Salary not listed
27 days ago
Sarah Cannon Research Institute
The Research Nurse is responsible for monitoring study subjects to ensure strict protocol compliance and patient protection. Key duties include screening patients, managing medication approvals, and accurately documenting clinical data and follow-up procedures.
28 days ago
McKesson
The Research Nurse is responsible for monitoring study subjects to ensure strict protocol compliance and patient protection. Key duties include screening patients, managing medication approvals, and accurately documenting clinical data and procedures.
Perform clinical and neurocognitive test evaluations and interview ratings on study participants according to protocol. Ensure data integrity and adherence to FDA, ICH, and GCP guidelines while assisting the Principal Investigator.
The Clinical Research RN I oversees daily clinical study activities and serves as a liaison between the investigative site and the Sponsor. Responsibilities include providing nursing care to participants, executing protocols, and ensuring ethical documentation of all research data.
$34 - $43 / HOUR
1 month ago
The Pharmacy Technician II coordinates the dispensing of investigational drugs for clinical trials while ensuring adherence to study protocols. They are responsible for monitoring storage temperatures, managing pharmaceutical supplies, and maintaining strict compliance with FDA and GCP guidelines.
Responsible for conducting basic to moderately complex diagnostic testing and managing laboratory samples according to study protocols. Duties include maintaining harvest logs, monitoring storage temperatures, and ensuring adherence to FDA and GCP guidelines.
$20 - $25 / HOUR
Performs diagnostic testing and basic laboratory activities across disciplines such as hematology and chemistry. Responsible for sample collection, storage, documentation, and adherence to FDA and GCP guidelines.
$19 - $23 / HOUR
Performs diagnostic testing and basic laboratory activities across disciplines such as hematology and chemistry. Responsible for sample collection, storage, and strict adherence to FDA and GCP guidelines.
$19 - $24 / HOUR
$20 - $21 / HOUR
The Clinical Rater is responsible for administering and scoring neurocognitive and clinical assessments to evaluate study participants' diagnostic and functional status. They ensure data integrity, maintain protocol adherence, and facilitate consensus rounds to support clinical research objectives.
The Psychiatric Technician interacts directly with patients in clinical trials, monitoring behavior and assisting with daily living activities. They also ensure adherence to study protocols, dietary restrictions, and medication administration under the guidance of medical staff.
The Psychiatric Technician interacts directly with patients in clinical trials, observing behavior and assisting with daily living activities. They also support the clinical team by ensuring protocol adherence, facilitating group activities, and assisting with medication administration.
The Psychiatric RN oversees daily clinical study activities and serves as a liaison between the investigative site and the sponsor. They are responsible for documenting research data, monitoring patient vitals, and ensuring adherence to clinical protocols and safety standards.
$39 - $49 / HOUR
2 months ago
The Research Nurse is responsible for screening, enrolling, and monitoring study subjects for blood cancer and bone marrow transplant clinical trials. They ensure protocol compliance, accurate data collection, and proper documentation of patient care and adverse events.
The Psychiatric RN is responsible for overseeing daily clinical study activities and serving as a liaison between the investigative site and the sponsor. They must accurately document clinical information, monitor study participants, and ensure adherence to research protocols and safety standards.
$37 - $46 / HOUR
OneOncology
The Research Nurse will execute clinical trials by screening, enrolling, documenting, and monitoring study subjects while ensuring strict protocol compliance and delivering exceptional patient care. Key duties include obtaining and maintaining informed consent, documenting study visits, monitoring patient safety, and managing investigational product dispensing.
The role is responsible for administering various clinical and neurocognitive test evaluations and interviews/ratings on study participants according to the protocol, including assessing cognitive, neuropsychological, behavioral, and functional status. Essential duties involve conducting clinical rating scales to confirm diagnoses, assisting the Principal Investigator (PI) in maintaining data integrity, and ensuring continuity of data collection among rating staff.
This role involves performing select diagnostic testing across laboratory disciplines like hematology, urinalysis, and chemistry, requiring minimal interpretation. Essential duties include maintaining laboratory logs, monitoring sample storage temperatures, preparing supplies, and ensuring strict adherence to clinical research regulations and SOPs.
