Develop and nurture strong Dyne Therapeutics – Clinical Trial Site relationships
Optimize site performance, particularly enrollment
Oversee CRO site management and monitoring activities
Build/support site relationships while ensuring quality monitoring oversight and delivery of data of high integrity
Work directly with internal study teams, CRO partners, and clinical trial sites

Requirements

Bachelor’s Degree or international equivalent required; Life Sciences preferred. Advanced degree highly desirable
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
Monitoring experience in rare disease preferred
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

Benefits

Health insurance
401(k) matching
Flexible work hours
Paid time off
Remote work options

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

clinical trial researchmonitoringsite managementenrollment optimizationdata integrityICHGCPonsite monitoringcentral monitoringstudy management

Soft skills

communicationattention to detailrelationship buildingoversightteam collaborationproblem-solvingorganizational skillsleadershipinterpersonal skillsadaptability

Certifications

Bachelor’s DegreeAdvanced degree