Description

Oregon Urology Institute is offering a Full-Time Clinical Research Coordinator opportunity. As one of the largest and most advanced urological centers in the Northwest, we provide patients with access to some of the region’s finest medical experts across all major urological specialties. Utilizing proven and leading-edge technologies such as robotic surgery, immunotherapy, and radiation therapy, our primary focus is on managing all aspects of patient care as per each study protocol’s requirements.

Company Culture and Environment

At Oregon Urology Institute, we emphasize a collaborative and respectful work environment. We are committed to fair treatment of our employees and prioritize maintaining a workplace free from discrimination and harassment. Our culture is built on mutual respect and integrity.

Career Growth and Development Opportunities

We encourage our team members to pursue research-specific certifications upon hiring, which reflects our commitment to ongoing professional development and career advancement opportunities.

Detailed Benefits and Perks

In addition to standard benefits, we offer fully employer-paid life, health, dental, and vision insurance, 6 paid holidays, generous PTO, and voluntary benefits. Our outstanding retirement plan further supports the well-being of our employees.

Compensation and Benefits

• Research Coordinator wage range: \(18.00 to \)24.00 per hour, DOE.
• Fully employer-paid life, health, dental, and vision insurance.
• 6 paid holidays and generous PTO.
• Voluntary benefits available.
• Outstanding retirement plan.

Why you should apply for this position today

This position offers the opportunity to work in a dynamic environment at a leading urological center. By joining our team, you will play a crucial role in conducting clinical trials and impacting patient care within the community.

Skills

• Medical office experience.
• Excellent communication skills.
• Initiative and a desire to learn.
• Ability to multitask in a fast-paced environment.
• Strong teamwork capabilities.
• Willingness to earn research-specific certifications upon hiring.
• Ability to process lab samples (blood and pathologic) as needed.

Responsibilities

• Ensure the sound conduct of clinical trials.
• Maintain accurate and complete documentation.
• Assist the department with the organizational management of all trial aspects.
• Communicate all protocol-related issues to the appropriate management staff.
• Develop enrollment and follow-up mechanisms.
• Manage enrollment and follow-up of study subjects.
• Prepare case report forms (CRF) and study documentation.
• Monitor and report adverse experiences.
• Coordinate sponsor and/or FDA audits.
• Conduct study close-out when necessary.

Qualifications

• Medical office experience required.
• Excellent communication skills are essential.
• Initiative and eagerness to learn.
• Ability to multitask in a fast-paced environment.
• Ability to work well in a team setting.
• Willingness to process lab samples as needed.

Education Requirements

• Baccalaureate in a health-related field preferred.

Education Requirements Credential Category

• Bachelor’s Degree in a relevant field.

Experience Requirements

• Two (2) years of clinical research-related experience preferred.
• Patient care experience is a plus.

Why work in Springfield, OR

Springfield offers a charming and welcoming community with easy access to beautiful natural surroundings. The city combines a rich history with modern amenities, making it an excellent place to live and work. Residents can enjoy a variety of outdoor activities, cultural events, and a strong sense of community, enhancing work-life balance.