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MedWiz of Mass LLC
Overview
The Staff Pharmacist is responsible for dispensing prescription medications, providing education on medication use, and collaborating with healthcare professionals to optimize patient care. They also conduct clinical verification of prescriptions and ensure quality assurance standards are met.
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Compensation
Salary not listed
Posted
8 days ago
The IV Technician is responsible for the sterile compounding and preparation of intravenous medications while adhering to strict safety and aseptic protocols. They also manage inventory levels and collaborate with healthcare professionals to ensure accurate and timely delivery of medications to patients.
MedWiz Solutions LLC
The IV Technician is responsible for preparing sterile intravenous medications by accurately measuring ingredients, compounding, and ensuring proper labeling and documentation according to established protocols. This role also involves performing quality control checks, monitoring inventory, and adhering strictly to aseptic techniques to maintain sterility.
ICON plc
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing data integrity, and overseeing drug accountability.
17 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.
24 days ago
St. Jude Children's Research Hospital
The role involves the experimental study of pediatric cancer dependencies and the identification of new therapeutic targeting approaches. Responsibilities include studying protein signaling, subcellular relocalization, and testing small molecule inhibitors.
1 month ago
Syneos Health
Provide patient-focused clinical services including mobile research nursing and patient concierge for pharmaceutical and biotechnology industries. Support clinical trials across various phases and therapeutic areas to improve the patient experience.
$67,700 - $115,100 / YEAR
Takeda
The Medical Support Specialist will determine donor eligibility through interviews, physical exams, and reviewing test results, while also managing donor adverse events and notifying donors of unsuitable test results. This role involves following SOPs for medical emergencies and providing center-level support for environmental, health, and safety matters.
$24 - $33 / HOUR
The role involves determining donor eligibility through medical history review, physical exams, and testing, while managing donor adverse events and notifying donors of unsuitable test results. The specialist will operate under the guidance of the Center Manager for operations and the Center Physician for medical issues, ensuring compliance with industry regulations.
$22 - $30 / HOUR
The role involves determining donor eligibility through medical history review, physical exams, and testing, while also managing donor adverse events and reviewing laboratory results. The specialist supports center operations under the guidance of the Center Manager and Center Physician.
The Medical Support Specialist will determine donor eligibility through interviews, physical exams, and reviewing test results, while also managing donor adverse events and notifying donors of unsuitable test results. This role involves following SOPs for medical emergencies and referring complex medical issues to the Center Physician or Medical Affairs.
$25 - $34 / HOUR
The Medical Support Specialist will determine donor eligibility through interviews, physical exams, and reviewing test results, while also managing donor adverse events and notifying donors of unsuitable test results. This role involves following SOPs for medical emergencies and referring complex medical or technical issues to the Center Physician or Medical Affairs.
M3USA
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening study participants, maintaining documentation, and ensuring compliance with research protocols.
GRAIL
The Clinical Project Assistant supports study teams in Clinical Operations by managing administrative aspects of clinical trial execution. Key duties include maintaining the Trial Master File, tracking site payments, and assisting with quality metrics and meeting coordination.
$33 - $39 / HOUR
The role involves determining donor eligibility through interviews, physical exams, and reviewing test results, while also managing donor adverse events and ensuring compliance with regulations. This position supports plasma center operations under the guidance of the Center Manager and Center Physician.
$32 - $44 / HOUR
The role involves determining donor eligibility through interviews, physical exams, and testing, while managing adverse donor events and reviewing laboratory results. The specialist operates under the guidance of the Center Manager for operations and the Center Physician for medical issues.
The Medical Support Specialist is responsible for screening donor eligibility, performing physical exams, and managing donor reactions according to standard operating procedures. They also collaborate with the center physician and support employee health programs to ensure a safe and high-quality plasma collection environment.
$26 - $35 / HOUR
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing site documentation, and overseeing drug accountability throughout the clinical trial process.
$91,336 - $114,170 / YEAR
Texas Health Resources
Responsible for the timely and accurate preparation, delivery, and storage of medications within the pharmacy department. Ensures adherence to quality improvement standards and patient safety initiatives while maintaining required competencies.
