About The Position

Join our dynamic research team and play a key role in advancing high‑impact studies that make a difference. As a Clinical Research Coordinator , you will work with talented investigators and departmental leadership to ensure the successful execution of one or more research projects. This role offers the opportunity to take on greater independence, contribute to scientific work, and help mentor others—all while supporting the operational excellence of the department. Key Responsibilities: Lead Research Coordination: Independently manage research and administrative tasks across one or more active studies, ensuring accuracy, compliance, and timely progress. Collaborate with Investigators: Partner closely with study investigators and your supervisor to proactively identify and resolve study‑related challenges. Provide Departmental Support: Serve as backup to other coordinators when needed and contribute to departmental financial performance through budgeting, billing, and related tasks. Contribute to Scientific Outputs: Develop specialized research instruments and assist in preparing scientific manuscripts and presentations. Support Study Operations: Provide occasional after‑hours and on‑call support as required, including occasional overnight business travel. Leadership & Advanced Skill Development: Demonstrate increased independence and productivity compared to an Associate Clinical Research Coordinatot. Train and mentor other research coordinators in proper study conduct and best practices. Participate in quality control activities as directed, ensuring the highest standard of research integrity. Providence Swedish caregivers are not simply valued – they’re invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Requirements

  • Bachelor's Degree Preferably in Science, Healthcare, or other related field --or-- Significant experience in research coordination may be substituted for educational requirements
  • 3 years of experience in related area

Nice To Haves

  • Upon hire: Certified Clinical Research Coordinator (CCRC) or similar professional research certification

Responsibilities

  • Lead Research Coordination: Independently manage research and administrative tasks across one or more active studies, ensuring accuracy, compliance, and timely progress.
  • Collaborate with Investigators: Partner closely with study investigators and your supervisor to proactively identify and resolve study‑related challenges.
  • Provide Departmental Support: Serve as backup to other coordinators when needed and contribute to departmental financial performance through budgeting, billing, and related tasks.
  • Contribute to Scientific Outputs: Develop specialized research instruments and assist in preparing scientific manuscripts and presentations.
  • Support Study Operations: Provide occasional after‑hours and on‑call support as required, including occasional overnight business travel.
  • Leadership & Advanced Skill Development: Demonstrate increased independence and productivity compared to an Associate Clinical Research Coordinatot. Train and mentor other research coordinators in proper study conduct and best practices.
  • Participate in quality control activities as directed, ensuring the highest standard of research integrity.

Benefits

  • Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security.
  • We take care of you, so you can focus on delivering our mission of improving the health and wellbeing of each patient we serve.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service