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University of Massachusetts Medical SchoolNew
Overview
The Research Associate I provides operational support to the laboratory by performing experiments and maintaining accurate research records. They are responsible for interpreting data, monitoring supply levels, and ensuring compliance with safety and institutional protocols.
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Compensation
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Posted
New
Rochester Regional Health
As a Licensed Practical Nurse, you will provide professional patient care to long-term and post-acute care residents while directing and monitoring the care provided by CNAs. You will ensure proper documentation and timely medication administration as per physician orders.
$28 - $34 / HOUR
2 days ago
Avera Health
The Nurse Practitioner will provide appropriate medical care by assessing the physical, psychological, and social dimensions of patients to develop a comprehensive plan of care. Responsibilities include diagnosing and treating patients according to approved protocols, providing health education, and performing necessary diagnostic and therapeutic procedures in collaboration with a physician.
Headlands Research
The Nurse Practitioner or Physician Assistant will serve as a Sub-Investigator, ensuring the safety and welfare of clinical trial subjects. Responsibilities include conducting medical history interviews, performing physical examinations, and reviewing lab results according to research protocols.
6 days ago
Avalo Therapeutics
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
7 days ago
Evolution Research Group
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They are responsible for ensuring protocol adherence, managing subject recruitment, and maintaining accurate regulatory documentation under the direction of the Principal Investigator.
9 days ago
IQVIA
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
$71,900 - $169,300 / YEAR
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They ensure protocol adherence, manage subject recruitment, and maintain accurate regulatory documentation under the direction of the Principal Investigator.
Beth Israel Lahey Health
The nurse will support clinical research trials by collaborating with multidisciplinary teams to implement protocols and monitor patient data. They will also provide direct patient care, including symptom management and recruitment for various oncology studies.
$36 - $79 / HOUR
10 days ago
Rapport Therapeutics
The Senior Clinical Trial Associate manages clinical study documentation, including the Trial Master File, to ensure inspection readiness and compliance with ICH-GCP standards. They also support the trial team with administrative tasks, vendor invoice tracking, and the preparation of essential study-related documents.
$90,000 - $110,000 / YEAR
11 days ago
Cleveland Clinic
The MRI Technologist will perform routine MRI exams and procedures on patients of all ages, ensuring they feel comfortable, safe, and properly informed throughout the process. Responsibilities also include preparing and validating patient safety forms, maintaining equipment, and coordinating data transmission.
14 days ago
COG Research Foundation, LLC
The Protocol Coordinator develops and maintains clinical research protocols, training materials, and study-related documents under scientific leadership. They manage internal and external review processes and coordinate communication between study chairs and committees to ensure trial activation.
$64,542 - $92,421 / YEAR
16 days ago
ICON plc
The Medical Research Associate is responsible for greeting clinical research volunteers and performing vital sign assessments and phlebotomy procedures according to study protocols. They also provide personalized care to study subjects and ensure their comfort throughout the research process.
M3USA
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
17 days ago
University of Kansas Medical Center
The Clinical Research Coordinator manages assigned clinical research studies by supervising complex activities involved in data collection, compilation, documentation, and analysis, while monitoring participants' progress and reporting adverse events. Responsibilities include recruiting and educating potential patients, maintaining source documents, performing study procedures, and ensuring compliance with GCP guidelines and FDA CFR.
$60,800 - $91,200 / YEAR
22 days ago
McLaren Health Care
Facilitates clinical research studies by evaluating candidate eligibility and managing the informed consent process. Coordinates study procedures, collects data, and ensures compliance with research protocols and regulatory requirements.
23 days ago
University of Rochester
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and regulatory bodies to ensure data accuracy and compliance.
$21 - $30 / HOUR
1 month ago
Cincinnati Eye Institute
The Clinical Research Coordinator oversees study protocols, ensures regulatory compliance, and manages site activities including patient recruitment and data documentation. They also coordinate with sponsors, manage study budgets, and perform study-specific testing and exams according to protocol guidelines.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with participant screening, maintaining documentation, and ensuring all activities comply with the research protocol and regulations.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with screening, maintaining documentation, collecting and entering data, and mentoring junior staff.
