Clinical Ethicist offers guidance to patients, their families, and professional staff on ethical, legal and policy issues and concerns stemming from clinical interactions between health care professionals and patients. Provides guidance to the institutional ethics committee pertaining to policy formulation and educational and case review activities. Being a Clinical Ethicist develops institutional policies concerning ethical issues such as "do-not-resuscitate" and "withdrawal of life-support". Requires a master's degree or doctorate related to health ethics. Additionally, Clinical Ethicist typically reports to a manager or head of a unit/department. To be a Clinical Ethicist typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. (Copyright 2024 Salary.com)
Job Overview:
Midwest Clinical Research, LLC is seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. The Clinical Research Coordinator will be responsible for assisting in the coordination and management of clinical trials, ensuring compliance with HIPAA regulations, and maintaining accurate documentation. This is an exciting opportunity for someone with a passion for research and patient care. The facility specializes in allergy, pulmonary disease, and vaccine trials.
Responsibilities:
- Coordinate and manage clinical trials from start to finish
- Ensure compliance with all applicable regulations, including HIPAA
- Review documentation for accuracy and completeness
- Assist in patient recruitment and screening processes
- Conduct patient monitoring and follow-up visits
- Collect and phlebotomize blood samples as required
- Monitor vital signs and document patient responses
- Maintain accurate and up-to-date records of all study-related activities
- Assist in data management and analysis processes
Requirements:
- Bachelor's degree in a related field (e.g., healthcare, life sciences), RN, LPN, or Respiratory Therapist preferred
- Previous experience working in clinical research or a related field required
-Phlebotomy experience required
- Knowledge of clinical trials management and regulatory standards
- Strong attention to detail and ability to maintain accurate documentation
- Excellent organizational and time management skills
- Ability to work independently as well as part of a team
-Ability to interact with a diverse patient population
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint) and able to learn a variety of Sponsor provided computer programs
- Excellent communication skills, both written and verbal
- Time Management skills are crucial
Our entire staff is dedicated to meeting the needs of Sponsors and contract research organizations for fast, efficient patient recruitment, compliance with protocol and regulatory guidelines, production of reliable data, and providing quality care to each patient. We offer competitive compensation packages and opportunities for professional development. If you are passionate about research and making a difference in patients' lives, we encourage you to apply for the position of Clinical Research Coordinator.
Job Types: Full-time, Part-time
Pay: $25.00 - $30.00 per hour
Expected hours: 40 per week
Benefits:
Experience level:
Schedule:
Ability to Relocate:
Work Location: In person