Clinical Research Coordinator
3 weeks ago
As a Clinical Research Coordinator at Christiana Care, you will play a crucial role in the implementation of protocol activities for patients entered into approved research studies. This includes evaluating potential participants for inclusion in specific protocols, informed consent, data and specimen collection and submission, adverse event reporting, and protocol compliance.
Responsibilities:
- Assist with the implementation of protocol activity for patients entered into approved research studies.
- Provide educational information and serve as a resource for participants and potential participants, significant others, physicians, medical staff, and the community regarding ongoing and upcoming clinical studies and protocol-specific disease management and prevention.
- Maintain local, national, and international standards of conduct for clinical trial participation.
- Collect, compile, and analyze data retrieved from ongoing clinical trials and submit follow-up case reports and adverse action reports.
Requirements:
- BSN required; or commitment to obtaining within three years of date of hire.
- Minimum 2 years acute care clinical experience.
Estimated Salary: $70,000 - $90,000 per year.
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