Medix™
Job Location : New York,NY, USA
Posted on : 2025-01-16T10:21:40Z
Job Description :
Key Responsibilities:
- Ensure optimal quality of medical care for patients participating in clinical studies, adhering to ethical standards for healthcare personnel.
- Assist in the creation and development of educational materials and manuals for patients and staff, serving as a reference framework for clinical practices.
- Engage in continuing education programs and actively educate nursing staff on drug protocols and new treatment methodologies.
- Contribute to the update and improvement of institutional policies and procedures, staying current with advancements in treatment options, including venous access devices.
- Arrange follow-up visits with patients to assess the quality of care, applying both physical and psychological assessments to monitor any effects of study drugs.
- Provide interventions in the event of adverse patient responses, ensuring their well-being throughout the study.
- Assess patient eligibility for inclusion in investigational studies by reviewing patient history, obtaining pre-study lab data, and securing baseline laboratory blood work and necessary scans.
- Review and explain informed consent with patients, and coordinate with medical personnel to ensure required follow-up tests are completed.
- Assist physicians in preparing IRB documents and maintaining communication with the sponsoring company/agency and IRB.
- Ensure adherence to study protocols, including the monitoring and administration of study drugs, conducting pharmaceutical studies, and performing laboratory procedures to process, store, and ship specimens.
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