Clinical Research Coordinator III

Innovative research paves the way for improved patient outcomes. You can be a part of the research that’s driving new treatments and procedures  your role, you will coordinate clinical trials, design and develop protocols and provide mentorship to other research staff. If you’re ready to grow your skills and share in the Legacy mission of making life better for others, we invite you to consider this opportunity.

• Coordinate multiple clinical trials as assigned, staying within the parameters of protocol and regulatory compliance, available resources, and budget. Demonstrates leadership and teamwork in work on projects.
• Coordinate patient enrollment and participation by reviewing study candidates’ medical records for eligibility, initiating enrollment, ensuring informed consent, and maintaining accurate enrollment records.
• Ensure administrative compliance with study protocols with respect to clinical procedures, laboratory tests and other patient activities; may administer study questionnaires, ensure drug self‑administration accountability with patients.
• Complete clinical requisition forms as instructed, assemble kits for patient visits, transport laboratory samples and ensure samples are processed and shipped according to study guidelines; track and maintain research supplies.
• Act as protocol liaison with clinical teams, patients, and providers on study related topics.
• Assist with maintaining appropriate source documentation and/or performing case report form data entry; respond to all data queries.
• Track and report adverse events per sponsor and institutional guidelines.
• Assists in development of workflow procedures for study team based on specific protocol.
• May travel to attend consortium and/or industry-sponsored meetings.

Education: Bachelor’s degree in a related field or equivalent healthcare experience.

Experience: Minimum of three years experience in clinical research coordination. Five or more years of experience preferred.

Skills:

• Competent in word processing, spreadsheet management, and database management and development.
• Excellent interpersonal skills, with outstanding written and verbal competencies.
• Demonstrated presentation skills.
• Excellent organizational and problem‑solving skills.
• Ability to work independently, handle multiple projects simultaneously, and manage conflicting priorities.
• Excellent mentoring and training skills.
• Extensive knowledge of clinical research, federal regulations and research administrative practices.
• Flexibility to work variable hours, as needed.
• Ability to share in taking calls.
• Ability to travel within the research community using personal or public transportation.
• Ability to travel to developmental and promotional activities.

Licensure: Must become certified as a Clinical Research Coordinator within one year of hire into this position.

Pay Range: USD $32.31 - USD $46.20 /Hr.

Our Legacy is good for health for Our People, Our Patients, Our Communities, Our World. Above all, we will do the right thing.

If you are passionate about our mission and believe you can contribute to our team, we encourage you to apply—even if you don't meet every qualification listed. We are committed to fostering an inclusive environment where everyone can grow and succeed.

Legacy Health is an equal opportunity employer and prohibits unlawful discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion or creed, citizenship status, sex, sexual orientation, gender identity, pregnancy, age, national origin, disability status, genetic information, veteran status, or any other characteristic protected by law.

To learn more about our employee benefits :(Use the "Apply for this Job" box below).-you