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Clinical Research Specialist - Cardiology
Corewell Health
Grand Rapids, Michigan, United StatesOn Site
Original Job Summary
Clinical Research Specialist - Cardiology
With principal investigator oversight, prepares, evaluates and implements research studies to enhance clinical practice.
Essential Functions
- Serves as primary coordinator and project manager for research studies.
- Evaluates and prepares studies including feasibility, budget, and protocol operations.
- Identifies, recruits, screens and enrolls eligible subjects per protocol.
- Monitors patient status, collects and documents data per protocol.
- Maintains studies in compliance with federal, state, and local law and policies.
- Coordinates study activities including adverse event identification and specimen management.
- Communicates and collaborates with study sponsors, clinical research office and multidisciplinary teams.
Qualifications
- Bachelor's degree in a health or science related field or equivalent.
- Basic Life Support certification within 90 Days of employment.
- Preferred 1 year of relevant experience in clinical research and project management.
- Proven cardiac related experience.
About Corewell Health
Corewell Health is a nationally recognized health system committed to personalized care and innovation. Team members enjoy comprehensive benefits and career development opportunities, alongside a collaborative culture that values diversity and inclusion.
Work Details
- Location: 330 Barclay, Grand Rapids
- Employment Type: Full time, Variable shift with potential weekends
- Hours: 40 hours/week, 8:00 a.m. to 5:00 p.m., Monday to Friday
Key skills/competency
- Clinical Research
- Project Management
- Cardiology
- Protocol Management
- Data Collection
- Compliance
- Subject Recruitment
- Feasibility Analysis
- IRB Documentation
- Team Collaboration
How to Get Hired at Corewell Health
🎯 Tips for Getting Hired
- Customize Resume: Highlight clinical research and project management experience.
- Tailor Application: Emphasize relevant cardiology exposure.
- Research Corewell Health: Understand their mission and values.
- Prepare for Interview: Review regulatory, compliance, and study coordination processes.
📝 Interview Preparation Advice
Technical Preparation
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Review clinical trial protocols.
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Understand IRB documentation requirements.
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Learn research data systems.
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Study regulatory compliance standards.
Behavioral Questions
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Describe your team collaboration experience.
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Explain handling stressful project deadlines.
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Share conflict resolution examples.
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Discuss effective communication with diverse teams.