Clinical Research Coordinator III - 238113

Medix™; Seattle (WA); On-site; Full time

Job summary

An established industry player is seeking a passionate Clinical Research Coordinator III to join their team in Seattle. This role involves engaging with patients for various Ophthalmology studies, ensuring a smooth and positive experience while coordinating trials effectively. With a focus on patient interaction, the ideal candidate will have a minimum of 3 years of experience and the ability to work autonomously with minimal training. This position offers a full-time contract with the potential for permanent placement based on performance. If you are motivated and ready to make a difference in clinical research, this opportunity is for you.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Paid Time Off

Qualifications

• Minimum 3 years as a Clinical Research Coordinator.
• Experience with industry-funded and PI initiated trials.

Responsibilities

• Pre-screening, consenting, and enrolling Ophthalmology patients for studies.
• Focus on patient interaction rather than data entry.

Skills

Clinical Research Coordination

Patient Interaction

Trial Coordination

Job description

Clinical Research Coordinator III - 238113

3 days ago Be among the first 25 applicants

This range is provided by Medix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$28.00/hr - $38.00/hr

Must Haves:

Must have minimum 3+ years as a Clinical Research Coordinator

Hours:

40 hours per week, Monday-Friday 8:30am-5pm, Onsite

Contract Duration:

4-6 month contract with the possibility to be hired on perm depending on performance

Benefits:

Medical, Dental, Vision, time off, etc.

Role & Responsibilities:

• Pre screening, consenting, enrolling and seeing Ophthalmology patients for 18 studies. The CRC they are looking for does NOT handle data entry and regulatory on the administrative end, so they are needing someone that is highly motivated and passionate about patient interaction.

Must Have Skills/Qualifications:

• 3 years experience as a CRC
• Experience on both industry funded and PI initiated trials. If they just have experience in one, it needs to be industry
• Ability to start with minimal training and know how to fully coordinate a trial (although they won't be responsible for any study start up). They will be trained on company processes and studies, but the expectation is that they know how to be autonomous

Apply Today!

Seniority level:

Associate

Employment type:

Full-time

Job function:

Research

Industries:

Hospitals and Health Care and Research Services

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