Vor Bio · 2 months ago
Senior Manager, Clinical Scientist
Boston, MA
Full-time
Onsite
Senior Level
6+ years expVor BioPharma is dedicated to tackling autoimmune diseases at their root through innovative science. The Senior Manager, Clinical Scientist plays a crucial role in supporting global clinical trials, ensuring scientific integrity and operational excellence throughout the study lifecycle.
BiotechnologyHealth CareOncologyPharmaceutical
Responsibilities
Contributes to preparation and/or review of any documents related to the studies and requiring a scientific background (abbreviated protocol/protocol/amended protocol, informed consent form, presentations/communication to internal or external partners, study plans including medical monitoring plan, safety management plan, risk mitigation plan and recruitment materials)
Assists in preparing medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts involved in the study/project
Contributes to the definition of the critical data/processes/predefined deviations list, risks and Quality tolerance limits identification and monitoring, to implement/develop related sections of the study risk management plan
Is involved in the update of study documents, ensures eCRFs are aligned with protocol updates, and contributes to optimizing and documenting data collection processes to enhance quality and reduce complexity
Supports Medical Monitors in subject-level data reviews, including eligibility assessments and ongoing data monitoring, ensuring timely data entry, consistency, and integrity
Supports data cleaning and query resolution throughout the study and participates in final review activities leading up to database lock to ensure data accuracy and integrity
Collaborates with Medical and Clinical Operations teams in developing study-specific training materials and provides scientific support during investigator and study team trainings
Contributes to definition of the centralized monitoring strategy in consistency with the planned statistical analysis and is involved in study data validation and review processes, support the director for the Clinical Case review (safety events reported to GPV or safety events of special interest), notably to anticipate and prevent last minute queries or backlog and smoothen the process
Qualification
Required
Advanced degree (PhD, PharmD, MD, or equivalent) in life sciences, medicine, or a related field
Minimum of 6 years in clinical research, with demonstrated leadership in clinical science roles
Familiar with digital tools such as data analytics or agility to use them
Ability to synthesize the information, good presentation skills and effective communication skills (verbal and written)
Strong knowledge of clinical trial design, methodology, and regulatory requirements
Excellent analytical, organizational, and communication skills
Ability to manage multiple projects and priorities in a fast-paced environment
Proven track record of cross-functional collaboration and team leadership
Benefits
Comprehensive health coverage
Flexible paid time off
Generous parental leave
Competitive 401(k)
Education assistance
Wellness resources
Financial security
Company
Vor Bio
Vor Bio is a clinical-stage biotechnology company transforming the treatment of autoimmune diseases.
2-10 employees
H1B Sponsorship
Vor Bio 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 (5)
2023 (6)
2022 (10)
2021 (1)
2020 (1)
Funding
Current Stage
Public CompanyTotal Funding
$748.4MKey Investors
RA Capital Management
2025-12-15Post Ipo Equity· $150M
2025-11-10Post Ipo Equity· $100M
2025-06-24Post Ipo Equity· $175M
Leadership Team
Jean-Paul Kress
Chairman and CEO
Dallan Murray
EVP, Chief Commercial Officer
Recent News
GlobeNewswire
2025-12-15
2025-12-15
Company data provided by crunchbase