About the job Senior Safety Domain Expert - Falcon
Job Title: Senior Safety Domain Expert - Falcon
Job Location: Boston, MA
Job Location Type: Remote
Job Contract Type: Full time
Job Seniority Level:
The Role
We are looking for an experienced pharmacovigilance professional to serve as our Senior Safety Domain Expert for Veeva Falcon. This role bridges ground-level case execution with macro-level safety operations, using your deep knowledge of case processing, MedDRA coding, database reconciliation, and global compliance to inform our AI driven automation tools. You will spend your days collaborating with our internal technical teams and external early adopters, acting as the definitive "Voice of the Customer" to ensure our platform delivers flawless safety automation.
- End-to-End Workflow Guidance: Advise product and engineering teams on the detailed steps of safety case intake, triage, validation, and advanced data reconciliation workflows
- Ground-Truth Verification: Actively review and verify platform outputs across initial data entry, automated MedDRA coding assignment, and generated follow-up queries to ensure absolute data precision
- Early Adopter Engagement: Interact directly with PV leads and processing specialists at early adopter organizations, translating their feedback into actionable platform enhancements
- Stress-Test Scenario Building: Map out highly complex, multi-variable safety case scenarios to rigorously evaluate and calibrate the platform's reasoning boundaries
- 5+ years of active experience in Pharmacovigilance / Drug Safety Operations
- Extensive hands-on knowledge of the complete case lifecycle, including validation criteria, database reconciliation, and global expedited reporting timelines
- High proficiency with MedDRA coding rules and deep familiarity with mainstream safety databases (e.g., Veeva Safety, Argus, ArisG)
- Strong collaborative mindset with the ability to confidently present operational perspectives to non-clinical technical partners and customers
- Prior experience contributing to the design, implementation, or user-acceptance testing (UAT) of automated pharmacovigilance intake solutions
- Prior experience with, or a strong baseline curiosity about, agentic AI, automated workflows, or next-generation cloud platforms in clinical trials
We value your time and believe in a transparent hiring process. Here is the process you can expect.
- Follow the application process and submit your resume.
- Within 3 days, you will receive a link to a personality assessment administered by a third party.
- Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
- If moving to the interview stage, the process is as follows:
- A conversation with the hiring manager
- A practical case exercise
- A final conversation with our group's Senior Leader.
- Once all interviews are complete, the manager will be in touch with a final decision.
- Medical, dental, vision, and basic life insurance
- Flexible PTO and company paid holidays
- Retirement programs
- 1% charitable giving program
- Base pay: $120,000 - $180,000
- The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
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