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Home Flexible Job Board Site Manager

$60,000–65,000/yr 6d ago

Site Manager

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Avania

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Full-time Permanent Remote

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Summary

The Site Manager will conduct ongoing outreach to clinical trial sites to ensure study progress, engagement, and adherence to expectations. They are responsible for managing site documentation, resolving action items, and supporting enrollment strategies across a portfolio of 30 to 40 sites.

Job Description

Avania is hiring Site Managers / CTA  

Salary range $60,000 - $65,000 + Annual performance related bonus + Benefits

About the role

As a Site Manager at Avania, you will play a key role in supporting clinical trial site operations through proactive site outreach and communication, helping sites stay organized, responsive, and aligned with study expectations. In this role, you will serve as a central point of contact for site-facing follow-up, partnering with investigational sites to close action items, support enrollment discussions, collect essential documents, and help maintain study documentation such as the TMF. This position is designed for clinical research professionals who already understand the site environment—particularly those coming from Study Coordinator, nursing, or similar site-level backgrounds—and are ready to move into the clinical operations side of the business. It offers a strong entry point into Avania for individuals who are not new to research, but are looking to broaden their experience in a fully remote-based role. With direct exposure to site management activities and clear long-term development options, this role offers an excellent next step for someone looking to build a career in clinical operations.

What you'll be doing

  • Conduct ongoing site outreach and communication to help keep assigned sites engaged, informed, and progressing against study expectations
  • Follow up on action items with sites, helping drive timely resolution of outstanding tasks and operational questions
  • Support discussions around enrollment strategies and site needs, helping sites stay focused on study goals and recruitment momentum
  • Collect and review essential documents required for study execution, helping ensure materials are submitted and tracked appropriately
  • Help maintain study documentation and support efforts to ensure the TMF remains current and organized
  • Communicate clearly with sites regarding expectations, timelines, and required next steps, acting as a reliable operational partner
  • Provide support related to site-facing processes such as documentation readiness and, where relevant, activities connected to IRB submissions
  • Manage a site workload that may involve approximately 30 to 40 sites, depending on study assignment and overall distribution

About the company

Avania

Avania is the only global CRO built for MedTech — integrating regulatory strategy, clinical development, and market access and reimbursement to take innovations from concept to commercialization with confidence. Avania was purpose-designed to serve medical technology innovators, combining regulatory, clinical, engineering, and market access expertise to guide products across the full lifecycle.

We bring deep experience across a wide range of therapeutic areas, with particular strength in cardiovascular, neurovascular, and orthopedics: three of MedTech’s most complex and high-growth fields. Avania combines international reach with deep local expertise. Our regional teams understand the regulatory, cultural, and operational nuances that accelerate approvals and improve site engagement worldwide.

Partner with Avania and experience the difference of a MedTech-only CRO: trusted expertise, collaborative engagement, and proven results.

Company size

201-500 employees

Industry

Medical Equipment Manufacturing

Org type

Privately Held

Headquarters

Marlborough, MA

Apply Now

About the company

Avania

Avania is the only global CRO built for MedTech — integrating regulatory strategy, clinical development, and market access and reimbursement to take innovations from concept to commercialization with confidence. Avania was purpose-designed to serve medical technology innovators, combining regulatory, clinical, engineering, and market access expertise to guide products across the full lifecycle.

We bring deep experience across a wide range of therapeutic areas, with particular strength in cardiovascular, neurovascular, and orthopedics: three of MedTech’s most complex and high-growth fields. Avania combines international reach with deep local expertise. Our regional teams understand the regulatory, cultural, and operational nuances that accelerate approvals and improve site engagement worldwide.

Partner with Avania and experience the difference of a MedTech-only CRO: trusted expertise, collaborative engagement, and proven results.

Company size

201-500 employees

Industry

Medical Equipment Manufacturing

Org type

Privately Held

Headquarters

Marlborough, MA

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