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CHS Recruiting
Overview
The physician will evaluate, diagnose, and treat cardiovascular disorders, perform non-invasive procedures, and manage patient care. They will also communicate with the clinical team to ensure quality care delivery.
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Compensation
$400,000 - $575,000 / YEAR
Posted
9 days ago
Medpace, Inc.
The Clinical Nurse will provide necessary nursing coverage for the Clinical Pharmacology Unit, adhering strictly to study protocols and Good Clinical Practice guidelines. Responsibilities include performing and documenting various clinical procedures, safely administering medications, assessing adverse events, and providing detailed end-of-shift reports for continuity of care.
Salary not listed
24 days ago
Essen Medical Associates
Provide comprehensive endocrine care and on-site consults for residents in skilled nursing and long-term care facilities. Manage complex metabolic and hormonal disorders while supervising nurse practitioners and interdisciplinary teams.
$215,000 - $240,000 / YEAR
25 days ago
Beth Israel Lahey Health
The candidate will support investigators by performing proteomic assays and conducting routine laboratory tests such as DNA sequencing and PCR analysis. They are also responsible for collecting study data, maintaining logs, and performing literature searches.
$19 - $26 / HOUR
Emory Healthcare
Provides comprehensive genetic counseling services across various clinical programs and supports laboratory operations through diagnostic testing coordination. Assists in the training of students and residents while participating in genetic research initiatives and professional presentations.
$41 - $49 / HOUR
1 month ago
Cleveland Clinic
Provide direct nursing care, monitor patient conditions, and implement care plans for patients undergoing bariatric surgery. Administer medications, coordinate discharge needs, and educate patients and their families on postoperative care.
The Nurse Practitioner will collaborate with a physician-led team to serve as a subject matter expert on neurology projects. Responsibilities include developing clinical education materials, participating in protocol development, and supporting study-related activities.
Nurse Practitioners will collaborate with a physician-led team and serve as subject experts on assigned projects. They will also develop clinical education materials and support study-related activities.
The Nurse Practitioner will develop and implement disease-specific education and review clinical safety data as part of the medical monitoring team. They will also assist with study participant recruitment and provide clinical expertise in business presentations.
The Medical Writer will write IND and NDA modules, clinical study reports, protocols, and amendments. They will also coordinate quality control reviews and interact closely with sponsors and subject matter experts.
The Clinical Safety Nurse will handle and process adverse events from various sources, including clinical trials and post-marketing surveillance. Responsibilities include determining action plans for incoming calls, collecting and tracking adverse events, writing safety narratives, and collaborating with internal departments.
The Clinical Safety Coordinator will collect, process, and track serious adverse event reports while generating safety narratives and performing quality control of safety cases. Collaboration with internal departments and clinical research sites is essential to ensure compliance with safety processes.
The Clinical Records Administrator supports TMF oversight for a trial by ensuring documents meet established quality standards. This role involves managing electronic filing systems, tracking documents, and communicating with internal associates globally.
The Study Start-Up Coordinator communicates with research sites to collect essential documents for clinical trials and maintains quality reviews of trial documents. They also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also manage timelines for study start-up and develop solutions to regulatory challenges.
The TMF Document Administrator supports TMF oversight for a trial by ensuring documents meet established quality standards. This includes managing the electronic filing system for trial documentation and communicating with internal associates regarding errors in trial documents.
The Clinical Trial Associate supports Trial Master File (TMF) oversight by ensuring all documents meet established quality standards, which involves managing electronic filing systems, tracking, maintaining, and performing quality checks on documents. This role also requires communication with internal associates globally regarding document errors and preparing documents for shipment.
The Clinical Nurse Study Coordinator is responsible for the accurate administration of medications, monitoring of adverse events, and performing clinical procedures according to study protocols. They also collaborate with project managers and investigators to ensure operational flow and data integrity.
2 months ago
Northwestern Memorial Healthcare
The Endocrinologist will manage a variety of endocrine disorders and contribute to the health and well-being of a diverse patient population. They will provide comprehensive evaluation, diagnosis, and treatment while developing long-term relationships with patients.
$280,000 - $300,000 / YEAR
The Endocrinologist will provide comprehensive evaluation, diagnosis, and treatment for a wide range of endocrine disorders, metabolic diseases, and hormonal imbalances. Responsibilities include managing a diverse patient population, developing long-term patient relationships, and working collaboratively within a multidisciplinary team in an outpatient setting.
