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Mass General Brigham
Overview
The Research Coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests like phlebotomy and EKGs. They also ensure study compliance, maintain regulatory binders, and prepare data for analysis.
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Compensation
$20 - $29 / HOUR
Posted
2 days ago
Weill Cornell Medical College
The Research Nurse Specialist executes various technical and administrative tasks related to specific clinical research studies, ensuring optimal quality of medical care and ethical conduct for participating patients. Responsibilities include educating staff on drug protocols, assisting with policy updates, and managing study documentation and specimen handling according to protocol.
$108,972 - $125,388 / YEAR
5 days ago
The Research Nurse Specialist is responsible for ensuring the optimal quality of medical care for patients enrolled in clinical research studies while maintaining ethical conduct. This includes assisting with the creation of educational materials for patients and staff, and educating nursing staff on drug protocols.
The Research Nurse Specialist ensures optimal quality of medical care and ethical conduct for patients in clinical research studies, assisting with educational materials and staff training on drug protocols. Responsibilities include assessing patient eligibility, managing follow-up visits, implementing interventions for adverse responses, and coordinating necessary laboratory work and scans.
The Research Nurse Specialist ensures optimal quality of medical care and ethical conduct for patients in clinical research studies, while also assisting in creating educational materials for patients and staff. Responsibilities include assessing patient eligibility, managing study drug monitoring, performing necessary laboratory procedures, and coordinating follow-up visits.
Nevada System of Higher Education
The Research Coordinator will recruit and screen clinical trial participants, manage regulatory documentation, and provide clinical care services including patient monitoring and sample processing. They will also assist with study budget proposals, data entry, and ensure adherence to institutional and federal protocols.
$25 - $37 / HOUR
8 days ago
Evolution Research Group
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
Salary not listed
9 days ago
Mercyhealth Wisconsin and Illinois
The Clinical Research Coordinator is responsible for recruiting and consenting study participants, managing regulatory documentation, and ensuring protocol adherence. They also handle specimen collection and processing while maintaining accurate data submission and reporting adverse events.
$27 - $42 / HOUR
Baylor Scott & White Health
The Radiologic Technologist performs radiology procedures on patients as requested by a physician or licensed provider to diagnose disease and injury, following established protocols. Essential functions include performing high-quality procedures, maintaining imaging quality, monitoring radiation dose, and communicating effectively with patients using AIDET.
10 days ago
Adams Clinical
The Mental Health Technician ensures participant safety and maintains a therapeutic environment within an inpatient research facility. Responsibilities include providing direct care, monitoring behavioral changes, documenting clinical data, and assisting with laboratory tasks.
$20 - $24 / HOUR
13 days ago
ICON plc
The Senior CRA will oversee clinical trial monitoring activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also conduct site visits, manage site performance, and collaborate with cross-functional teams to ensure accurate data collection.
17 days ago
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. This involves conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
The Senior CRA oversees clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They conduct site visits, manage data collection, and provide training to site staff to ensure successful trial execution.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Conduct site visits to assess performance, resolve issues, and collaborate with cross-functional teams for accurate data reporting.
The Research Nurse Specialist ensures optimal quality of medical care and ethical conduct for patients in clinical research studies, assisting with educational materials for staff and patients. Responsibilities include assessing patient eligibility, managing study drug protocols, performing necessary assessments, and implementing interventions for adverse patient responses.
19 days ago
Tandem Intermediate LLC
The Clinical Research Assistant supports daily clinic operations and ensures study procedures are followed according to protocol guidelines. Key duties include collecting and processing laboratory samples, screening patients, and maintaining regulatory documentation.
21 days ago
Prisma Health
The role involves providing primary healthcare to a specific patient population, engaging in the diagnosis and treatment of ailments, and managing required documentation for care and billing purposes. Responsibilities also include participation in educational programs, proposal responses for managed care, and contributing to quality assurance and operational development initiatives.
27 days ago
Johns Hopkins Medical Management Corporation
The technologist performs diagnostic sonographic and interventional procedures under supervision, consistently selecting appropriate equipment and protocols based on patient needs and study requirements. They must obtain complete, quality images, accurately take measurements, provide preliminary findings to the interpreting physician, and adhere to aseptic techniques.
$40 - $48 / HOUR
28 days ago
University of Rochester
Coordinates administrative and clinical activities for human subject research projects focusing on muscular dystrophy. Responsibilities include participant recruitment, regulatory document management, and overseeing data integrity for clinical trials.
$21 - $30 / HOUR
1 month ago
AstraZeneca
Field Clinical Advisors are crucial for the successful execution of cell therapy clinical trials by driving recruitment, retention, and safety management while generating early insights. They focus on clinical study protocol expertise, educating sites, optimizing the patient journey, and engaging with the cell therapy pipeline.
$197,000 - $295,000 / YEAR
