Clinical Research Coordinator

Are you passionate about making a difference in the field of clinical research? Do you have a keen eye for detail and a dedication to ensuring the highest quality standards are met? If so, we invite you to apply for the position of Clinical Research Coordinator at Missouri Cancer Associates.

About the Role:

As a Clinical Research Coordinator , you will play a crucial role in advancing medical knowledge and improving patient outcomes through clinical trials. In this onsite position, you will be responsible for the recruitment, screening, consenting, and enrollment of patients in clinical trials, ensuring that each trial is conducted with the utmost adherence to protocol requirements and regulatory standards.

Benefits:

We offer a competitive benefits package, including:

• Medical Insurance
• Dental Insurance
• Vision Insurance
• Life Insurance
• Short Term Disability Coverage
• 401k Retirement Plan
• Paid Time Off
• A Wellness Program that rewards healthy lifestyle practices

• Patient Recruitment & Enrollment: Screen potential patients for eligibility, present trial concepts, and guide them through the informed consent process to enroll them in clinical trials.
• Protocol Compliance: Coordinate patient care in strict compliance with protocol requirements, including disbursing investigational drugs and maintaining accountability.
• Data Collection & Documentation: Collaborate with physicians to monitor patients for changes in condition, adverse events, and protocol compliance. Document findings meticulously and participate in data collection.
• Regulatory Compliance: Prepare study-related documentation, maintain regulatory documents, and participate in auditing and monitoring visits to ensure compliance with US Oncology Research SOPs and applicable regulations.
• Training & Education: Lead educational initiatives for clinic staff regarding clinical research processes and collaborate on action plans for performance improvement.
• Reporting & Financial Management: Compile and report protocol activity, accrual trends, and financial information. Review protocol-specific billing guides and submit billing information as needed.

• Education: An Associate's degree in a clinical or scientific discipline is required; a Bachelor's degree is preferred.
• Experience: A minimum of three years in a clinical or scientific discipline, highly recommended oncology experience. Clinical research experience is highly valued.
• Certification: SoCRA or ACRP certification is preferred.Skills: Proficiency in Microsoft Office, excellent communication and organizational skills, strong multi-tasking and time management abilities, and exceptional attention to detail.
• Interpersonal Skills: Strong ability to interact with individuals at all levels, fostering a collaborative and professional environment.

Working Conditions:

Environment: This position is based in a traditional office setting within an oncology/hematology clinic. You may encounter exposure to communicable diseases and medical preparations.

Physical Requirements:

The role involves extensive computer-based work, standing, and walking. Occasionally, you may need to lift items up to 40 lbs.

Why Join Us?

Impactful Work: Contribute to groundbreaking clinical research that has the potential to change lives.
Professional Growth: Engage in ongoing training and development opportunities to enhance your skills and expertise.
Collaborative Team: Work alongside dedicated professionals who are committed to excellence and innovation in clinical research.

If you are ready to take the next step in your career and join a dynamic team at the forefront of clinical research, we would love to hear from you. Apply today to become a part of our mission to advance healthcare and improve patient outcomes.