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American Addiction Centers
Overview
Coordinates activities for multiple cardiology research studies, serving as the primary administrative liaison. Responsibilities include patient recruitment, obtaining informed consent, and managing data submission to sponsors.
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Compensation
$27 - $40 / HOUR
Posted
18 days ago
Baptist Health South Florida
The Research Associate 3 is responsible for collecting, analyzing, and interpreting research data. They must ensure high-quality research performance and adhere to organizational guidelines when presenting outcomes.
$58,495 - $76,043 / YEAR
19 days ago
Cedars-Sinai
The Clinical Research Associate I will assist in coordinating and implementing non-complex research studies, including tasks such as data collection, scheduling participants, and ensuring compliance with guidelines. The role involves supporting supervising staff with regulatory submissions and maintaining research practices.
Salary not listed
21 days ago
Boys Town
Assists in the execution of research studies through data collection, equipment maintenance, and the preparation of stimuli. Responsible for recruiting human subjects and reporting project outcomes to the principal investigator.
25 days ago
The Research Associate 3 is responsible for collecting, analyzing, and interpreting research data. They must ensure all research outcomes are presented in accordance with Baptist Health South Florida guidelines and maintain high-quality research standards.
26 days ago
The Research Associate 3 will be responsible for collecting, analyzing, and interpreting collected data. They will adhere to Baptist Health South Florida guidelines when presenting research outcomes and ensure high-quality research is performed.
$58,494 - $76,043 / YEAR
The Research Associate 3 is responsible for collecting, analyzing, and interpreting research data within the surgical administration department. They must ensure all research outcomes adhere to Baptist Health South Florida guidelines and maintain the highest quality standards.
27 days ago
The Research Associate 3 is responsible for collecting, analyzing, and interpreting data generated from research activities. This role requires adherence to Baptist Health South Florida guidelines when presenting research outcomes to ensure the highest quality of research is maintained.
$55,801 - $72,541 / YEAR
Children's Healthcare of Atlanta
The Research Pharmacist manages investigational pharmaceutical care by evaluating and implementing research drug protocols. Responsibilities include the procurement, storage, and dispensing of study medications while ensuring compliance with state and federal regulations.
29 days ago
Tufts Medicine
This role involves assisting the Principal Investigator in planning and implementing clinical research studies, including participant recruitment, screening, and follow-up activities. Responsibilities also cover maintaining regulatory compliance, managing study documentation, performing basic lab activities, and coordinating data collection and query resolution.
$47,924 - $59,895 / YEAR
Administer and score psychological and neuropsychological test batteries to evaluate cognitive, behavioral, and emotional status. Provide technical support to clinicians and assist in the preparation of diagnostic reports and treatment plans.
1 month ago
University of Rochester
Coordinates administrative activities for multi-site clinical research studies, including participant recruitment and consent. Manages study visits, ensures regulatory compliance, and assists in disseminating research findings through publications.
$21 - $30 / HOUR
University of Miami
The APP provides advanced medical care and nursing interventions for oncology patients, focusing on diagnosis, treatment, and recovery. They also manage clinical trial eligibility, patient enrollment, and protocol compliance within the oncology service line.
The Research Assistant will support laboratory operations by performing data collection, equipment calibration, and subject recruitment for human or animal research studies. They are also responsible for maintaining detailed records, preparing test materials, and assisting in the construction and maintenance of laboratory electronic devices.
The Registered Nurse 2 delivers patient-family centered care in an infusion center and medical ambulatory clinic, overseeing daily nursing practice. Responsibilities include assessing patients, administering medications, coordinating care, and educating patients and families on treatment plans.
The role involves planning, coordinating, and implementing clinical research studies while ensuring adherence to regulatory guidelines and protocol standards. Responsibilities include managing participant enrollment, maintaining research records, and performing quality checks to ensure data accuracy and participant safety.
$25 - $35 / HOUR
The Advanced Practice Registered Nurse (APRN) delivers medical care to patients, performing examinations, diagnosing conditions, and prescribing treatments. The role involves collaboration with healthcare professionals and ensuring quality patient care through various clinical responsibilities.
2 months ago
UCSF
The incumbent will perform entry-level duties to support and coordinate clinical studies for participants with language difficulties at the UCSF Memory and Aging Center. Responsibilities include recruiting and scheduling subjects, managing study data, preparing protocols, and assisting with clinical trial documentation.
$38 - $61 / HOUR
INSIGHT Surgical Hospital
The Clinical Research Coordinator will support principal investigators, act as a liaison between sponsors and the institute, and oversee the details of clinical studies, ensuring compliance with review boards and regulations across multiple research projects. Key duties include providing technical support, directing trial operations, managing enrolled patients, maintaining regulatory documents, and reporting adverse events to all governing bodies.
3 months ago
University Hospitals
The role involves providing safe, age-specific nursing care to patients within the framework of clinical research protocols, collaborating with the Principal Investigator to implement assigned studies according to GCP guidelines. Key duties include managing regulatory document submissions, recruiting participants, obtaining informed consent, educating subjects, completing documentation, and conducting nursing assessments.
