Entrada Therapeutics · 18 hours ago
Clinical Trial Manager
Boston, MA
Full-time
Onsite
Senior Level
$136K/yr - $163K/yr
7+ years expEntrada Therapeutics is a clinical-stage biopharmaceutical company focused on developing innovative therapies for patients. The Clinical Trial Manager will lead the planning, execution, and closeout of clinical trials, ensuring compliance with regulatory standards and effective communication with stakeholders.
BiotechnologyEmergency MedicineGeneticsHealth CareMedical
Responsibilities
Ownership of all operational aspects of designated clinical trial, including CRO and vendor management
Support and manage various study activities, including vendor evaluation and selection, country and site selection, informed consent development and maintenance, eCRF design and implementation, protocols, study plans and manuals, IBs, CSRs
Proactively identify and support resolution/escalation of trial conduct-related issues
Lead or support cross-functional trial teams, including collaborating with internal team members and external vendors for the planning and execution of clinical trials, through closeout
Provide regular up-to-date trial information and regular updates on trial progress/performance to internal stakeholders (enrollment, eligibility, protocol deviations, AE reporting etc.)
Oversee clinical monitoring from site qualification to site closure visits to assure integrity of clinical data with respect to accuracy, accountability and documentation through review of case report forms, source documents, and medical records
Support the review/cleaning and reconciliation of all clinical data, including EDC, PROs, and 3rd party labs to support timely database lock and the accurate analysis of clinical data
Partner with relevant stakeholders to develop and implement appropriate study-specific training to all relevant study-related personnel (internal, CRO, Site staff, and other relevant 3rd parties)
Support development of department documentation, such as SOPs
Help develop, organize, and maintain study budgets, working with business operations to ensure accurate forecasting
Support monitoring activities and visit clinical study sites as needed
Qualification
Required
BA/BS degree with 7 + years of combined experience supporting and independently managing clinical trial activities
Strong knowledge of ICH/GCP and regulatory requirements, with a strong preference for experience with global trials and EU-CTR
Strong experience in the drug development process, including trial design, trial planning and management, and CRO and vendor oversight
Excellent verbal and written communication skills
Proven ability to work effectively across functions
Ability to travel approximately 20% of the time, as determined by the needs of the business
Benefits
Comprehensive health, dental and vision coverage
Life and disability insurance
401(k) match
Paid, gender-inclusive parental leave
Holistic support for your health and well-being
Education reimbursement
Discretionary time off
Commuting benefits aligned to your working model
Company
Entrada Therapeutics
Entrada Therapeutics is a developer of novel therapeutics intended to treat devastating diseases.
51-200 employees
H1B Sponsorship
Entrada 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 (7)
2024 (14)
2023 (4)
2022 (6)
2021 (1)
2020 (1)
Funding
Current Stage
Public CompanyTotal Funding
$301.6MKey Investors
Wellington Management
2024-06-24Post Ipo Equity· $100M
2022-12-08Post Ipo Equity· $26M
2021-10-29IPO
Leadership Team
Dipal Doshi
Chief Executive Officer
Leo Qian
Co-Founder
Recent News
BioWorld Financial Watch
2026-01-11
2025-12-17
Company data provided by crunchbase