Senior Site Manager
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Avania
US
Summary
The Senior Site Manager will oversee clinical trial site operations from feasibility through initiation, ensuring sites are prepared and compliant with study protocols. They will perform remote monitoring activities, including source data verification, while providing guidance and mentorship to team members.
Job Description
Avania is hiring - Senior Site Manager
Salary range $75,000 - $80,000 + Annual Performance Related Bonus + Benefits
About the role
As a Senior Site Manager at Avania, you will play a key role in supporting clinical trial site operations from feasibility through site initiation, helping ensure sites are prepared, organized, and equipped to begin study activities successfully. In this role, you will serve as a knowledgeable partner to sites and internal teams, guiding essential document collection, protocol and training readiness, and start-up coordination with confidence and clarity. What differentiates this senior-level position is the ability to perform remote monitoring activities, including remote source data verification (SDV), making it well suited for professionals with prior CRA or in-house monitoring experience who are looking to apply their expertise in a less travel-intensive role. You will collaborate closely with CRAs and cross-functional stakeholders, bring structure and sound judgment to site-facing work, and may also provide mentorship to more junior team members. With meaningful ownership, broad exposure across the site lifecycle, and the opportunity to help drive quality site readiness, this position offers a strong next step for an experienced clinical research professional.
What you'll be doing
- Manage and support clinical trial sites from feasibility through site initiation, helping drive readiness for study start-up activities
- Guide sites through essential document collection, protocol understanding, and training requirements to support timely and compliant activation
- Build strong working relationships with sites, providing clear communication and practical direction on what is needed to get set up appropriately
- Perform remote monitoring activities, including remote source data verification (SDV), in alignment with study and sponsor requirements
- Review site documentation and study information with a detail-oriented approach to help ensure completeness, accuracy, and operational readiness
- Partner with field-based CRAs by supporting site-related activities that can be effectively managed remotely
- Apply prior monitoring or site management knowledge to identify issues early, escalate when needed, and help maintain momentum across start-up and site support tasks
- Contribute at a senior level by sharing expertise, supporting consistency in ways of working, and mentoring junior team members where appropriate
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
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