Clinical Research Coordinator - 257205

Medix™; Bellevue (WA); On-site; USD 65,000 - 80,000; Full time

Job summary

Medix is seeking a full-time, onsite Clinical Research Coordinator in Bellevue, WA to support Phase II–IV trials, coordinating patient visits, screenings, and data collection.

You will work with physicians, sponsors, and research teams, perform informed consent discussions, manage regulatory files, and ensure enrollment goals are met. 1+ year of clinical research experience and a college degree preferred.

Qualifications

• 1+ year of clinical research experience.
• College degree preferred or significant relevant experience.
• Strong organization, attention to detail, and communication skills.
• Ophthalmic experience preferred.

Responsibilities

• Coordinate daily clinical trial activities and patient visits.
• Screen and enroll eligible research participants.
• Conduct informed consent discussions and collect medical histories.
• Collect and document adverse events and study data.
• Perform clinical research procedures including labs, ECGs, tonometry, and pupil exams.
• Maintain source documentation, regulatory files, and study records.
• Enter and review data in EDC systems and resolve queries.
• Coordinate monitor visits and support sponsor/IRB requirements.
• Collaborate with the clinical team to achieve enrollment goals.

Skills

Organizational skills

Attention to detail

Communication skills

Ophthalmic experience

Education

College degree preferred or significant relevant experience

Job description

We are seeking a full time, onsite Clinical Research Coordinator in Bellevue, WA

Location: Bellevue, WA

Schedule: Full time, onsite

Monday- Friday 8AM-5PM

Pay: 65K-80K (Depending on experience)

We’re seeking a Research Coordinator to support the coordination and execution of Phase II–IV clinical trials, working closely with patients, physicians, sponsors, and research teams.

What you’ll be doing:

• Coordinate daily clinical trial activities and patient visits
• Screen and enroll eligible research participants
• Conduct informed consent discussions and collect medical histories
• Collect and document adverse events and study data
• Perform clinical research procedures including labs, ECGs, tonometry, and pupil exams
• Maintain source documentation, regulatory files, and study records
• Enter and review data in EDC systems and resolve queries
• Coordinate monitor visits and support sponsor/IRB requirements
• Collaborate with the clinical team to achieve enrollment goals

What we’re looking for:

• 1+ year of clinical research experience
• College degree preferred or significant relevant experience
• Strong organization, attention to detail, and communication skills
• Ophthalmic experience preferred

This is a great opportunity for a Research Assistant/Coordinator looking to take the next step in their clinical research career and gain hands-on experience across a variety of clinical trials.