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EPM Scientific

Clinical Specialist

burlingame, KS

Check who can apply and the requirements below before continuing.

About this opportunity

EPM Scientific lists this Clinical Specialist opportunity in burlingame, Kansas. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Looking for more than just another monitoring role?

If you're a Clinical Research Associate who wants greater ownership, closer access to leadership, and the opportunity to contribute beyond routine site monitoring, this could be your next move.

You would be working with a global specialty pharmaceutical company developing and commercializing innovative therapies for patients with severe genetic, metabolic, and life-threatening disorders. As the company continues to expand its clinical footprint, we’re seeking a CRA to help drive the successful execution of clinical studies across North America.

Why this opportunity stands out

Work directly with Clinical Operations and Global Clinical Affairs leadership

Gain broad study exposure beyond traditional CRA responsibilities

Join a growing biotech where your contributions are highly visible

Partner with leading investigators and research sites

Be part of a mission-driven organization developing therapies that change patients' lives

What you'll be doing

You’ll serve as the primary point of contact for assigned clinical sites, supporting studies from start-up through close-out while ensuring the highest standards of quality and compliance.

Responsibilities include:

Site qualification, initiation, monitoring, and close-out visits

Building strong relationships with investigators and site staff

Driving data quality, protocol compliance, and study execution

Supporting patient recruitment and site performance

Maintaining inspection-ready study documentation

Collaborating cross-functionally with Clinical Operations and study teams

What we're looking for

2–4 years of clinical research experience

CRA, Clinical Research Coordinator, or similar clinical operations background

Independent monitoring experience

Strong understanding of ICH-GCP and clinical trial conduct

Passion for quality, collaboration, and improving patient outcomes

What's on offer

Competitive salary and benefits

Exposure to both clinical and commercial aspects of drug development

Direct interaction with world-class scientific experts

Significant career growth potential within a fast-growing organization

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Worksite address

burlingame, KS, 66413, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.

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