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Professional Case ManagementNew
Overview
The Certified Mobile Research Nurse is responsible for scheduling and conducting mobile visits for pediatric study participants. They must perform physical assessments, collect specimens, and submit accurate source documentation in coordination with project managers.
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Compensation
$65 / HOUR
Posted
New
Professional Case Management
Responsible for scheduling and conducting mobile clinical visits for adolescent study participants. Tasks include performing physical assessments, phlebotomy, and submitting accurate source documentation.
$55 / HOUR
2 days ago
Responsible for scheduling and conducting mobile clinical research visits for pediatric participants aged 0-21. Tasks include performing physical assessments, collecting specimens, and submitting accurate source documentation.
3 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
9 days ago
Headlands Research
The coordinator is responsible for managing all aspects of research protocols to ensure integrity and quality according to GCP guidelines. Key duties include performing visit procedures, managing study supplies, and providing high-level care to study patients.
$70,000 - $75,000 / YEAR
10 days ago
Duke Careers
This role involves managing all aspects of clinical research operations within the Anesthesiology Clinical Research Unit, including preparing FDA regulatory submissions, managing investigational products, and ensuring protocol compliance across various settings.
$59,829 - $99,960 / YEAR
12 days ago
Care Access
The Clinical Research Coordinator I, RN conducts delegated clinical tasks and monitors research participants to ensure compliance with protocols and regulations. They are responsible for patient coordination, documentation, and recruitment activities.
Salary not listed
21 days ago
Rovia Clinical Research
Coordinate and execute clinical trials by conducting patient visits and performing clinical tasks like phlebotomy and ECGs. Ensure data integrity through accurate source documentation and EDC entry while maintaining protocol adherence.
$20 - $24 / HOUR
22 days ago
The CRA II manages and oversees clinical study sites to ensure data quality and patient safety in compliance with ICH-GCP and local regulations. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.
$80,000 - $110,000 / YEAR
Pinnacle Clinical Research
The Pharmacy Assistant supports day-to-day clinical trial operations, including receiving, documenting, and dispensing investigational products. They are also responsible for maintaining pharmacy logs, coordinating temperature calibrations, and providing patient education.
23 days ago
Alcanza Clinical Research
The role involves preparing and dispensing investigational medications and providing drug-related information to subjects and staff. It requires maintaining strict compliance with GCP, FDA, and USP standards while managing inventory and storage conditions.
27 days ago
Best Care
Coordinates clinical research studies including regulatory compliance, study start-up, subject follow-up, and record maintenance. Manages trial oversight, participant safety, and the handling of investigational products.
28 days ago
The US Oncology Network
The Clinical Research Nurse manages oncology patients throughout their journey by screening for clinical trials and conducting the informed consent process. They are responsible for administering investigational products, assessing adverse events, and ensuring accurate trial documentation.
1 month ago
K2 Staffing LLC
Provide PRN clinical support for clinical trials, including IV line maintenance and administration of investigational products. Assist Principal Investigators and coordinators with trial procedures while ensuring patient safety and adherence to GCP.
Alliance For MultiSpecialty Research LLC
Manages clinical research study tasks with a specialized focus on investigational product handling, administration, and subject safety. Coordinates trial activities in compliance with FDA regulations, GCP guidelines, and protocol-specific requirements.
Pathos
The role focuses on maintaining the Trial Master File and coordinating operational workflows between sites, CROs, and vendors to ensure inspection-ready FDA submissions. Additionally, the position involves identifying opportunities to automate clinical workflows using AI systems to accelerate trial timelines.
$75,000 - $85,000 / YEAR
The Clinical Research Coordinator coordinates and executes clinical trials by managing patient visits and ensuring adherence to study protocols and GCP guidelines. Key duties include performing clinical tasks, managing data entry in EDC systems, and maintaining investigational product accountability.
$50,000 - $55,000 / YEAR
Hawthorne Health
Assist the Principal Investigator in managing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all clinical trial data.
$150 / HOUR
The Investigational Product Coordinator is responsible for preparing and dispensing study drugs while ensuring compliance with regulatory standards like GCP, ICH, and HIPAA. They also provide drug-related information to subjects and staff while maintaining accurate inventory records and storage conditions.
United Urology Group
The Research Coordinator will screen, enroll, and monitor study subjects for clinical trials while ensuring strict adherence to protocols and regulatory standards. Responsibilities include managing study documentation, coordinating with investigators, and performing clinical procedures such as venipuncture and specimen collection.
