Senior Manager, Clinical Scientist

Join Us in Tackling Autoimmune Disease at Its Root

At Vor we believe science can do more than manage symptoms. It can change the course of disease. By advancing telitacicept a first- and potentially best-in-class dual BAFF/APRIL inhibitor we are silencing upstream survival signals and stopping downstream autoimmune cascades. Together we are addressing disease at its root cause and rewriting what is possible for patients worldwide.

When you join Vor youre not just working on a medicine. Youre part of a mission to redefine the future of autoimmune care.

Why Work at Vor

Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases.

Growth: Be part of a rapidly scaling company with opportunities to grow your career in science clinical development commercial strategy and beyond.

Innovation: Work on a platform with potential beyond one indication a therapy that has already shown consistent results across lupus IgA nephropathy and Sjögrens syndrome.

Belonging: Join a culture where every voice is heard and where our shared mission unites us across functions and geographies.

Senior Manager Clinical Scientist

Overview

TheSenior Manager ClinicalScientistplays a pivotal role insupporting global clinical trials by ensuring scientific integrity data quality and operational excellence from study design through database lock. This position combines strategic planningwithhands-on scientific expertise serving as a key bridge across clinical departmentstodrive collaboration and ensure high quality study execution.

Key Responsibilities

• Contributes to preparation and/or review of any documents related to the studies and requiring a scientific background (abbreviated protocol/protocol/amended protocolinformed consent form presentations/communication to internal or external partners studyplans including medical monitoring plan safety management plan risk mitigation plan and recruitment materials).

• Assistsinpreparingmedical 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 documentsensures eCRFs are aligned with protocol updates and contributes to optimizing and documenting data collection processes to enhance quality and reduce complexity.

• SupportsMedical Monitors in subject-level data reviews including eligibility assessments and ongoing data monitoring ensuring timely data entry consistency and integrity.

• Supportsdata cleaning and query resolution throughout the study and participatesin final review activities leading up to database lock to ensuredata accuracy and integrity.

• Collaborates with Medical Pharmacovigilanceand 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 theHead of PVfor Clinical Case review (allsafety events) notably to anticipate and prevent last minute queries or backlog and smoothen the process.

Qualifications

• Education: Advanced degree (PhD PharmD MD or equivalentexperience) in life sciences medicine or a related field.

• Experience: Minimum of6years 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.

Core Competencies

• Strategic Thinking: Ability to anticipate challenges identify opportunities and develop innovative solutions.

• Scientific Rigor: Commitment to high-quality research and evidence-based decision-making.

• Leadership: Skilled at motivating teams mentoring staff and fostering a culture of excellence.

• Communication: Effective at presenting complex scientific concepts to diverse audiences.

The salary range for the Senior Manager Clinical Scientist is expected to be between $160000 and $175000 per year. Individual pay may vary based on multiple factors including but not limited to relevant job-related skills experience education or training market factors and work location.

At Vor we support our team with robust benefits including comprehensive health coverage flexible paid time off generous parental leave and a competitive 401(k). From education assistance to wellness resources and financial security we invest in your well-being so you can thrive at work and beyond.

As an equal opportunity employer we at Vor Bio know that diversity inspires innovation inclusiveness and creativity. We invite you to come as you are. All applicants will be considered for employment agnostic to race age color religion sex sexual orientation gender identity national origin veteran or disability status.

Please visit our website at for more information.