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Ann & Robert H. Lurie Children's Hospital of Chicago
Overview
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
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Compensation
$49,920 - $81,619 / YEAR
Posted
6 days ago
Headlands Research
Ensure the safety and welfare of study subjects while conducting clinical research trials. Responsibilities include screening potential subjects, conducting medical history interviews, and providing medical care as needed.
Salary not listed
7 days ago
Ensure the safety and welfare of each study subject while conducting clinical research trials. Responsibilities include screening potential study subjects, conducting medical history interviews, and providing medical care as needed during participation in clinical trials.
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
21 days ago
Alcanza Clinical Research
The Clinical Research Coordinator ensures the execution of assigned studies in compliance with regulations and protocols. Responsibilities include patient screening, data entry, and maintaining communication with clients and team members.
23 days ago
The Clinical Research Coordinator ensures the execution of clinical studies in compliance with GCP, ICH, and FDA regulations. Key duties include patient screening, consenting, performing clinical procedures, and maintaining accurate study documentation.
1 month ago
The Clinical Research Nurse ensures the execution of assigned studies by performing clinical procedures and maintaining compliance with study protocols and regulatory standards. Responsibilities include patient screening, obtaining vital signs, documenting in source charts, and managing study-related data and supplies.
Sanford Health
The RN Clinical Research Coordinator will coordinate patient visits and assist with lab orders and screenings for neuro and vascular clinical research trials. This role involves managing complex components of clinical trials and ensuring compliance with research protocols.
$28 - $44 / HOUR
Alliance for Clinical Trial in Oncology Foundation
The Clinical Research Associate will manage clinical trial operations, including site selection, study start-up, and maintenance of trial master files. They will collaborate with CROs and investigative sites to ensure compliance with ICH GCP guidelines and organizational standards.
2 months ago
Ardelyx
The Clinical Research Associate II provides sponsor oversight of assigned investigative sites, focusing on high-quality protocol execution and compliance with GCP and regulatory requirements. This role involves monitoring site performance through data review, supporting all phases of the clinical trial lifecycle, and ensuring timely collection and maintenance of essential regulatory documents.
$99,000 - $121,000 / YEAR
ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES PC
The Clinical Research Nurse manages assigned unblinded protocols, ensuring compliance with regulations, and is responsible for preparing and dispensing investigational medication for IV or SC administration across various sites. This role acts as the primary liaison for unblinded site staff during clinical trials and coordinates all related monitoring visits.
Lurie Children's Hospital
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, overseeing all aspects from document preparation to study conduct across departments. Responsibilities also include managing participant engagement, collecting specimens, recording data, and assisting with financial aspects like invoicing.
CEDAR HEALTH RESEARCH LLC
The Clinical Research Coordinator is responsible for the successful execution of clinical trials under the principal investigator's supervision, handling both clinical tasks like performing procedures and administrative duties related to research conduct at the site. This includes ensuring adherence to all regulatory guidelines (GCP, ICH, FDA) and managing site staff training and trial operations.
3 months ago
Astera
The Clinical Research Coordinator will provide overall coordination for study-related activities for patients in cancer research studies, ensuring activities adhere to local and federal regulations and sponsor policies. Responsibilities include assisting with IRB submissions, maintaining regulatory documents, coordinating patient tests and visits, and entering research data into a centralized database.
The Clinical Research Coordinator ensures the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs, involving tasks like patient screening, consent, follow-up visits, and meticulous documentation in source charts and EDC systems. Responsibilities also include performing basic clinical procedures such as vital signs, ECGs, and potentially blood specimen collection, storage, and shipping.
The Principal Investigator is responsible for conducting and coordinating daily clinical trial activities in compliance with all relevant guidelines, protocols, and company policies. This role involves providing overall site leadership focused on enhancing efficiencies, ensuring patient safety, and maintaining protocol and regulatory compliance.
The Principal Investigator is responsible for conducting and coordinating daily clinical trial activities while ensuring the medical well-being and safety of study participants according to all relevant guidelines and protocols. This role involves overall site leadership focused on enhancing efficiencies, patient safety, and maintaining protocol and regulatory compliance.
Structure Therapeutics
The Senior Clinical Trial Associate serves as a central contact supporting the clinical study team in planning, implementing, and completing studies by interacting with sites, vendors, and team members. Key duties include obtaining, reviewing, and tracking study documents, setting up and maintaining the Trial Master File (TMF/eTMF), and facilitating meeting preparations.
$110,000 - $120,000 / YEAR
The Principal Investigator is responsible for conducting and coordinating daily clinical trial activities while ensuring the medical well-being and safety of study participants according to all relevant guidelines and protocols. This role involves overall site leadership focused on enhancing efficiencies, patient safety, and maintaining protocol/GCP/regulatory compliance.
4 months ago
Laborie Medical Technologies Corp
The Senior Clinical Research Associate oversees site management activities, including site selection, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also serve as a primary liaison between internal teams, vendors, and clinical sites to drive patient enrollment and maintain high-quality data standards.
