Senior Clinical Research Associate

RBW Consulting; United States; Remote; USD 65,000 - 75,000; Full time

Job summary

A leading medical device company is seeking a Senior Clinical Research Associate (CRA) for a US-based remote position involving significant national travel. This role will focus on managing investigational sites for pivotal Class III cardiovascular trials, emphasizing GCP compliance and proactive issue resolution.

Qualifications

• Minimum 5 years of independent monitoring experience in Class III medical device trials.
• Proven ability to manage 15 or more sites across multiple states.
• Deep understanding of GCP, ISO 14155, and FDA regulations.

Responsibilities

• Monitor 15+ investigational sites ensuring compliance and protocol adherence.
• Act as liaison between sponsor and site staff.
• Support site start-up, activation, monitoring, and close-out visits.

Skills

Site relationship management

Monitoring

Issue resolution

GCP knowledge

Regulatory compliance

Job description

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Senior Clinical Research Associate (CRA) – Cardiovascular Medical Devices

As a recruiter with deep roots in the clinical operations space, I’m proud to represent a growing, mission-driven medical device company at the forefront of cardiovascular innovation. This is the kind of company where your work doesn’t get lost in red tape where the patients come first, the team is tight-knit, and your contributions are seen and valued from Day 1.

We’re currently seeking an experienced Senior Clinical Research Associate (CRA) to join their expanding clinical team. This is a US-based, remote position with national travel (~40-50%) and the opportunity to manage 15+ active sites as part of a pivotal Class III cardiovascular trial.

???? Why This Role?

• High-impact studies: You’ll be hands-on with complex, Class III implantable cardiovascular devices that have the potential to save and extend lives.
• Lean, agile team: No layers of bureaucracy just close collaboration with a leadership team that trusts your judgment and empowers you to act.
• Room to grow: Be part of a company that’s scaling up and investing heavily in clinical trials, offering ample opportunity to step up as trials expand globally.

What You’ll Be Doing

• Monitoring 15+ investigational sites across the US ensuring compliance, GCP standards, and protocol adherence.
• Acting as the primary liaison between sponsor and site staff.
• Supporting site start-up, activation, monitoring, and close-out visits.
• Identifying and resolving issues proactively to ensure timelines and data integrity.
• Collaborating cross-functionally with clinical project managers, regulatory, and QA teams.
• Minimum 5 years of independent monitoring experience within Class III medical device trials (cardiovascular preferred).
• Proven ability to manage 15 or more sites across multiple states.
• Willingness and ability to travel up to 40% of the time, including overnight.
• Deep understanding of GCP, ISO 14155, and FDA regulations for medical devices.
• Based in the United States with the ability to work autonomously and communicate proactively with cross-functional teams.
• Experience in pre-market or IDE trials.
• Strong site relationship management and mentoring skills.
• A passion for working in small, entrepreneurial environments where everyone wears multiple hats.

Interested in learning more before applying?

Let’s talk I’m happy to share more about the company, the team, and how this role fits into their broader clinical strategy.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Strategy/Planning, and Administrative

• Industries

  Medical Equipment Manufacturing

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