Dyne Therapeutics · 14 hours ago
Associate Director, Clinical Site Liaison
United States
Full-time
Hybrid
Lead/Staff, Director/Executive
$155K/yr - $190K/yr
8+ years expDyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. The Clinical Site Liaison is responsible for developing and nurturing strong relationships with clinical trial sites, optimizing site performance, and overseeing CRO site management and monitoring activities to ensure quality and timely delivery of data.
BiotechnologyHealth CareMedicalPharmaceutical
Responsibilities
Enhance the development and maintenance of Dyne’s relationships with clinical investigators and site staff
Provide an interface among study sites, Dyne Therapeutics and CRO partners to create an optimal environment for clinical trials, enabling timely and high-quality output
Coordinate regular, fit for purpose, communication with clinical sites to align interactions with CRO and relevant internal stakeholders to assure a harmonized approach to site relationship and optimize site performance and quality delivery
May attend SIVs and Motivational/Booster visits/calls in collaboration with CRO partner
Maintain an operational knowledge of the protocol(s), answer site/CRO questions as applicable and assist in the escalation process in connecting site/CRO to Dyne Therapeutics personnel
Leverage experience and deep insight from interactions with clinical sites to provide strategic input on effective recruitment, outreach, and optimization strategies
Maintain and assist with the development of plans and tools to carry out these strategies, as appropriate
In collaboration with CRO partners and as approved by the Clinical Operations Study Lead (COSL), perform on-site visits in support of continued site engagement and data quality, identify and remove barriers to performance and to oversee on-site outsourced monitoring activities
Document and communicate observations from onsite monitoring activities (such as key areas of risks and noncompliance)
Provide ongoing risk assessment review of available data resources, review the site performance/CRO monitoring performance to identify trends, risks, and opportunities
In collaboration with the COSL, perform review of monitoring visit reports (on-site and central review reports) completed by CRO partner
Contribute to process improvements and knowledge/ sharing of best practices
Qualification
Required
Bachelor's Degree or international equivalent required; Life Sciences preferred
Strong knowledge of ICH/GCP
At least 8 years of relevant clinical trial research experience
Onsite/central monitoring and/or clinical lead/study-management experience
Clinical site facing experience required
Biotech or pharma industry experience is required
Experience overseeing/managing outsourced site management and monitoring activities
Excellent verbal and written communication skills
Excellent attention to details
Ability to travel, 30% or more frequently at times
Preferred
Monitoring experience in rare disease preferred
Advanced degree highly desirable
Company
Dyne Therapeutics
Dyne Therapeutics is a developer of targeted therapies intended for serious muscle diseases.
51-200 employees
H1B Sponsorship
Dyne Therapeutics has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (6)
2024 (7)
2023 (1)
2022 (3)
2021 (6)
Funding
Current Stage
Public CompanyTotal Funding
$1.67BKey Investors
Hercules CapitalAtlas Venture
2025-12-09Post Ipo Equity· $402.5M
2025-06-30Post Ipo Equity· $230M
2025-06-30Post Ipo Debt· $100M
Leadership Team
John Cox
Chief Executive Officer
Recent News
2026-01-11
2026-01-07
2025-12-24
Company data provided by crunchbase