Lead prescriptive discovery and design sessions for life sciences event management.
Deliver fast, high-quality implementations using Vault Platform and automation tools.
Guide customers through ecosystem integration and compliance reporting.
Veeva Systems is a mission-driven industry cloud pioneer helping life sciences companies bring therapies to patients faster. With over $3B in revenue, it fosters a culture of customer success, employee success, and speed.
Lead risk management and safety data review for assigned products, ensuring regulatory compliance.
Provide safety-related content for clinical and regulatory documents, and prepare for inspections.
Mentor a small pharmacovigilance team while driving end-to-end operational oversight.
Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies for blood cancer patients. We maintain a start-up culture of camaraderie and leadership by example, with a small dedicated team.
Lead pharmacovigilance strategy and operations across the portfolio, ensuring regulatory compliance and safety oversight.
Oversee outsourced PV vendors, build quality systems, and manage safety data exchange agreements.
Partner cross-functionally with Clinical Development, Regulatory, and Quality to advance pipeline from early to late-stage development.
Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies for autoimmune diseases. It is a lean organization with a build-oriented culture, advancing a pipeline from Phase 1 to Phase 3.
Act as a trusted advisor to customers and clinical sites, ensuring trial designs meet goals and providing training.
Lead database development activities, configure forms and rules in Vault CDMS, and build custom SQL listings.
Support requirements gathering, user acceptance testing, and risk management to keep projects compliant.
Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies, it surpassed $3B in revenue and is a public benefit corporation committed to balancing stakeholder interests.
Serves as main point of contact for adverse event questions and reviews in safety and clinical databases.
Performs quality control checks and finalization of cases in the Argus database.
Assists in oversight of case processing vendor and preparation of safety reports for regulatory agencies.
Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies for blood cancer patients. The company maintains a start-up culture of camaraderie and leadership by example.
Independently manage ICSR triage, case processing, and quality control for global safety reports.
Perform SAE reconciliation between safety and clinical databases, ensuring compliance with timelines.
Support team development through training, onboarding, and process improvement initiatives.
This company is a partner organization focused on global pharmacovigilance operations. It is a fast-growing, internationally focused company with a collaborative culture emphasizing teamwork, excellence, and continuous improvement.
Lead global pharmacovigilance audits, regulatory inspections, and readiness planning.
Oversee issue management, deviations, root-cause analysis, and CAPA activities.
Develop and manage the global pharmacovigilance training program and procedural documentation.
Our partner is a fast-growing biopharmaceutical company focused on improving outcomes for patients with severe autoimmune diseases. It offers a collaborative environment with opportunities for professional growth and leadership development.
Act as a trusted advisor configuring Veeva Vault CDMS for clinical trial data management.
Develop SQL-based custom listings and support data integrations and user acceptance testing.
Collaborate with customers, CROs, and vendors on study design and go-live activities.
Veeva Systems is a mission-driven cloud software company helping life sciences firms bring therapies to patients faster. As a fast-growing public benefit corporation with over $3B in revenue, it values customer success, employee success, and speed while supporting flexible work anywhere.
Lead customer-facing software implementation projects for global life sciences clients.
Design data solutions and configure Veeva Network MDM to unify customer and product data.
Connect systems, advise stakeholders, and coach junior team members to drive project success.
We are a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue and are a public benefit corporation committed to balancing customer, employee, society, and investor interests.
Lead a Professional Services team of EHS and Vault Platform experts, driving Customer Success.
Drive Implementation Excellence with prescriptive scoping and packaged solutions.
Build trusted executive relationships and manage escalations with humility.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year and are committed to making a positive impact on customers, employees, and communities.
Be the product evangelist and subject matter expert for Veeva EDC and Veeva DQS, communicating product roadmap directions.
Provide product education to customers in meetings and online communities, ensuring clear communication of value and functionality.
Act as customer advocate, gather and prioritize feedback, and collaborate with product teams to inform release planning.
Veeva Systems is a mission-driven industry cloud pioneer helping life sciences companies accelerate therapy delivery. As a fast-growing public benefit corporation with over $3B in revenue, it values customer and employee success.
Manage the intake, review, analysis, and reporting of Individual Case Safety Reports (ICSRs) and support Clinical Events Committees and Data Monitoring Committees.
Co-author and maintain study-specific safety documents and prepare aggregate safety reports for regulatory submission.
Collaborate with sponsors, study teams, and cross-functional partners to ensure data quality and compliance with GCP and GVP standards.
This partner company delivers high-quality safety services across clinical research and medical device programs. They foster a collaborative, detail-oriented environment with a focus on compliance and patient outcomes.
Review protocols and support design and configuration of eCOA.
Build, design and consult on eCOA solutions.
Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.
You will own complex software implementations from kickoff to go-live, managing 10-20 concurrent projects.
You will configure client applications using no-code flow builders and conduct quality assurance for regulatory submissions.
You will coordinate cross-functionally and scale implementation operations by developing SOPs and mentoring team members.
Veeva Systems is a mission-driven company and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, it surpassed $3B in revenue in its last fiscal year with extensive growth potential ahead.
Conduct discovery and needs analysis to understand customer requirements.
Deliver compelling demonstrations of Veeva Quality Cloud applications.
Lead workshops, pilots, and proofs of concept to help customers envision business process enhancements.
Veeva Systems is a pioneer in industry cloud, helping life sciences companies speed therapies to patients. As one of the fastest-growing SaaS companies, it surpassed $3B in revenue and is a public benefit corporation committed to balancing customer, employee, society, and investor interests.
Lead quality assurance activities to support patient safety and pharmacovigilance compliance across global operations.
Plan, conduct, and manage pharmacovigilance audits, CAPA programs, and regulatory inspection readiness activities.
Collaborate with cross-functional teams including clinical development, regulatory affairs, and medical affairs to maintain robust quality systems.
This company is a science-driven healthcare organization focused on pharmacovigilance and patient safety. They operate in a collaborative, global environment committed to operational excellence and meaningful healthcare impact.
Build and administer EDC trials using Veeva CDMS for client projects.
Perform eCRF design, edit check programming, and test data creation.
Manage interface connections and ensure high-integrity database imports.
Celerion is an agile clinical research organization that uses translational medicine to accelerate drug development. The company values integrity, trust, teamwork, and respect and seeks performance-oriented, innovative team players.
Lead client-facing safety projects and serve as the primary point of contact for pharmacovigilance services.
Manage project scope, timelines, and deliverables while coordinating activities across PV teams.
Provide pharmacovigilance expertise including ICSR processing, aggregate reporting, and quality review.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. It uses a shortlisting process to ensure fair and objective application review, and the final hiring decisions are made by the partner company.
Provide support to other activities undertaken by the project team on behalf of the client and the company.
Create and maintain project-specific KPIs for contracted ICSR activities, proposing process changes to the ICSR Operational Lead.
Manage ICSR deviations, review trackers and timesheet data for accuracy, and operate as the assigned team SME.
PrimeVigilance is a global pharmacovigilance specialist that helps clients navigate complex regulations while keeping patient safety at the center of every decision. The company operates across Europe, North America, South America, Asia, and Australia in a culture built on kindness, flexibility, growth, and belonging.
Lead global Pharmacovigilance Operations, Quality & Compliance strategy to ensure scalable, inspection-ready systems.
Oversee case processing, vendor governance, PSMF, quality systems, audits, and regulatory inspections.
Build and mentor a global team, collaborating cross-functionally to support portfolio growth and commercialization.
Ultragenyx is a biopharmaceutical company focused on developing life-changing treatments for rare diseases. They foster a supportive and inclusive culture of learning and growth, aiming to be an organization where employees can thrive personally and professionally.