What are the responsibilities and job description for the CLINICAL RESEARCH COORDINATOR-ONCOLOGY position at CommonSpirit Health?
CommonSpirit Health was formed by the alignment of Catholic Health Initiatives (CHI) and Dignity Health. With more than 700 care sites across the U.S. from clinics and hospitals to home-based care and virtual care services CommonSpirit is accessible to nearly one out of every four U.S. residents. Our world needs compassion like never before. Our communities need caring and our families need protection. With our combined resources CommonSpirit is committed to building healthy communities advocating for those who are poor and vulnerable and innovating how and where healing can happen both inside our hospitals and out in the community.
The CommonSpirit Health Research Institute, a beacon of medical advancement, offers comprehensive clinical research services and support for various research activities. Their primary focus includes multi-site clinical trials, local and large-scale data research, partnerships with industry and academia for technology and innovation research, physician-initiated research, resident-initiated research in teaching facilities, nurse-initiated research, and health sciences student-initiated research. By providing start-to-finish research services, they play a pivotal role in advancing medical knowledge and ultimately, patient care.
While you're busy impacting the healthcare industry, we'll take care of you with benefits that include :
Medical / Dental / Vision, FSA, Dependent Care Spending Account, Life Insurance, Short and Long-term Disability, 401k match, Paid Time Off, Wellness Program, Tuition Reimbursement, Accidental Insurance, Critical Illness Insurance, Identity Theft Protection, Employee Assistance Program, and more!
- Responsibilities
- This position is located at Mercy Medical Center-Merced. We will consider candidates who would need to relocate with relocation assistance offered and a sign on bonus of up to 10% of annual salary._
- Manage all aspects of assigned clinical research studies, including participant recruitment, screening, enrollment, data collection and study closeout
- Collaborate with investigators and research staff to develop and implement study protocols
- Ensure compliance with all regulatory requirements and ethical guidelines
- Maintain accurate and complete study documentation
- Build and maintain positive relationships with study participants and research staff
- Stay abreast of current research trends and best practices
- Qualifications
- Required Education and Experience :
- Strong background in clinical research
- Bachelors degree in a science or health-related field or equivalent experience
- Minimum of 3 years of experience conducting clinical trials required; worked as a primary research coordinator for at least 5 drug or device trials focused on the oncology specialty
- Pay Range
We are seeking a highly motivated and organized Clinical Research Coordinator-Oncology to join our growing team. In this role, you will play a vital role in supporting clinical research studies specific to the therapeutic area of oncology. You will work closely with principal investigators, research staff, and study participants to ensure the successful execution of research protocols.
The CRC's responsibilities encompass a wide range of tasks, including :
LI-CSH
29.00 - $42.00 / hour
We are an equal opportunity / affirmative action employer.
Salary : $29 - $42
