Role OverviewThe Clinical Research Coordinator will assist with collaborative studies in supportive care, coordinating study visits, managing data, and preparing study reports. The role requires working with a diverse group of professionals, including oncologists, palliative care clinicians, and other specialists. The coordinator will assume responsibility for study coordination, including screening and recruiting study participants, administering screening instruments, and managing data.
What You Will Do
The Clinical Research Coordinator will perform tasks such as screening and recruiting study participants, administering screening instruments, managing data, corresponding with regulatory departments, and preparing study reports. The coordinator will also assist with data analysis and preparation of manuscripts and conference presentations.
Why It Might Be a Fit
Ideal candidates will have an attention to detail, the ability to manage fluctuating priorities and deadlines, and strong interpersonal skills. Previous experience in research is preferred, and a Bachelor’s degree is required. A background or interest in psychology, medicine, nursing, or public health is preferred but not required.
Requirements
- Bachelor’s degree
- Previous experience in research (preferred)
- Background or interest in psychology, medicine, nursing, or public health (preferred)
- Excellent communication and organizational skills
- Ability to work independently
- Attention to detail
- Ability to manage fluctuating priorities and deadlines
- Strong interpersonal skills
Benefits
- Competitive base pay
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses
- Recognition programs
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