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Medpace, Inc.New
Overview
The Clinical Records Administrator supports TMF oversight for a trial by ensuring documents meet established quality standards. This role involves managing electronic filing systems, tracking documents, and communicating with internal associates globally.
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Compensation
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Posted
New
The TMF Document Administrator supports TMF oversight for a trial by ensuring documents meet established quality standards. This includes managing the electronic filing system for trial documentation and communicating with internal associates regarding errors in trial documents.
The Clinical Research Documentation Coordinator supports Trial Master File (TMF) oversight by ensuring all documents meet established quality standards for a clinical trial. Responsibilities include managing the electronic filing system, tracking, maintaining, and performing quality checks on documents, and communicating errors to internal associates globally.
The Clinical Trial Associate supports Trial Master File (TMF) oversight by ensuring all documents meet established quality standards, which involves managing electronic filing systems, tracking, maintaining, and performing quality checks on documents. This role also requires communication with internal associates globally regarding document errors and preparing documents for shipment.
Minneapolis heart institute foundationNew
Coordinates and leads clinical research studies, ensuring compliance with legal and regulatory standards from planning through closure. Manages patient recruitment, informed consent, data collection, and regulatory documentation for cardiovascular trials.
$65,000 - $75,000 / YEAR
Nationwide Children's Hospital
Coordinates clinical research trials for gene therapy, ensuring patient safety and protocol compliance. Manages data, regulatory elements, and collaborates with multidisciplinary care providers to facilitate positive patient outcomes.
2 days ago
ELEVATE CLINICAL RESEARCH, INC.
The Clinical Research Coordinator manages daily clinical trial operations, including patient recruitment, informed consent, and scheduling. They ensure strict compliance with regulatory requirements and GCP guidelines while maintaining accurate study documentation and data integrity.
UT Southwestern Medical Center
Provides data management and coordination for local and national research studies under the direction of an Investigator. Responsibilities include identifying eligible subjects, managing IRB submissions, and performing basic clinical procedures like phlebotomy and EKGs.
Provides data management and coordination for local and national research studies under the direction of an Investigator. Responsibilities include identifying eligible subjects, managing IRB documentation, and performing basic clinical procedures like phlebotomy and EKGs.
3 days ago
The Clinical Research Coordinator manages the daily operations of clinical trials, including patient recruitment, scheduling, and informed consent. They ensure strict compliance with regulatory requirements and GCP guidelines while maintaining accurate study documentation and data integrity.
ICON plc
Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Collaborate with investigators to maintain high-quality clinical data and prepare essential study documentation.
$91,336 - $114,170 / YEAR
University of Mississippi Medical Center
Coordinate and conduct research projects, including the recruitment, data collection, and retention of participants according to study protocols. Ensure all activities adhere to FDA guidelines, safety standards, and institutional policies.
Greenlife Healthcare Staffing
Perform routine and complex diagnostic EEG testing using advanced neurodiagnostic equipment. Responsibilities include preparing patients, applying electrodes, and documenting findings to support neurological assessments.
$58 / HOUR
4 days ago
Trinity Health
Support laboratory departments by collecting, processing, and analyzing specimens through venipuncture and other collection methods. Ensure data integrity by accurately registering specimens in the Laboratory Information System and maintaining safety standards.
Mass General Brigham
The Research Assistant is responsible for recruiting and screening study subjects, conducting clinical visits, and performing pulmonary testing. They also manage study data collection, lab processing, and the maintenance of regulatory documents for asthma research protocols.
$29 / HOUR
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
SHELTER, Inc.
Manage a caseload of up to 25 households, providing intake, assessment, and personalized care planning for survivors of domestic violence and supportive housing participants. Coordinate with community resources and maintain detailed documentation in the HMIS system to track participant progress and housing stability.
$30 - $32 / HOUR
Provide data management and coordination for clinical research studies, specifically focusing on the collection and distribution of human biospecimens. Responsibilities include consenting patients, communicating with clinical staff, and maintaining study documentation and databases.
Manage data for local and national research studies and coordinate the collection and distribution of human biospecimens. Interact with clinical staff and patients to explain study purposes and obtain informed consent.
Iterative Health
The Clinical Research Coordinator II manages daily clinical trial activities, including protocol management, patient recruitment, and study visit coordination. They are responsible for ensuring data integrity, maintaining regulatory documentation, and serving as the primary point of contact for study participants.
5 days ago
