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Emory HealthcareNew
Overview
Procures, prepares, and distributes medications and pharmaceutical supplies under the supervision of a registered pharmacist. Maintains inventory, operates pharmacy automation, and ensures compliance with USP, DEA, and FDA guidelines.
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Compensation
$25 - $30 / HOUR
Posted
New
Iterative Health
The Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures like blood draws and IV administration. They also ensure data integrity, maintain study documentation, and act as the primary point of contact for study participants.
Salary not listed
2 days ago
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
CSL
Responsible for the efficient collection of plasma from donors through venipuncture and monitoring the pheresis process according to SOPs. Duties include donor set-up, equipment troubleshooting, and maintaining accurate electronic donor records.
$21 - $30 / HOUR
3 days ago
4 C Medical Technologies
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
$75,000 - $95,000 / YEAR
6 days ago
Responsible for the efficient collection of plasma from donors through venipuncture and monitoring the pheresis process. Ensures donor safety and product quality while maintaining compliance with SOPs and FDA guidelines.
7 days ago
Responsible for the efficient collection of plasma from donors through venipuncture and monitoring the pheresis process. Ensures donor safety and product quality while maintaining accurate electronic records and equipment calibration.
9 days ago
Novartis
The Medical Science Liaison (MSL) will leverage scientific expertise and market knowledge to establish professional relationships and engage with Healthcare Providers (HCPs) and thought leaders, focusing on emerging data, clinical trials, and unmet medical needs within the assigned territory. Responsibilities also include informing and shaping medical strategy by collecting actionable insights and collaborating cross-functionally to advance clinical practice.
$145,600 - $297,700 / YEAR
Responsible for the efficient collection of plasma from donors through venipuncture and monitoring the pheresis process. Duties include donor set-up, equipment calibration, and ensuring compliance with SOPs and FDA guidelines.
10 days ago
11 days ago
Emory Healthcare
13 days ago
The Clinical Research Coordinator manages industry-sponsored clinical trials, including patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and investigators.
14 days ago
The Clinical Research Coordinator manages the daily activities of industry-sponsored clinical trials, including patient recruitment and visit coordination. They are responsible for clinical tasks like blood draws and ECGs, while ensuring strict adherence to study protocols and regulatory guidelines.
The CRC II manages industry-sponsored clinical trials, overseeing patient recruitment, study visits, and the collection of clinical data. They are responsible for maintaining high-quality documentation and coordinating communication between sponsors, CROs, and the Principal Investigator.
The CRC II manages industry-sponsored clinical trials by coordinating daily activities, leading patient recruitment, and conducting study visits. They are responsible for specimen processing, data entry into CTMS, and maintaining communication with sponsors and PIs.
The Clinical Research Coordinator manages industry-sponsored clinical trials, focusing on patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and investigators.
$19 - $20 / HOUR
16 days ago
The CRC II manages industry-sponsored clinical trials, focusing on patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and PIs.
22 days ago
University Hospitals
Coordinate and implement clinical research studies in GI while providing safe, age-specific nursing care to participants. Manage regulatory documentation, recruit participants, and ensure compliance with GCP and sponsor guidelines.
23 days ago
