Jobs at Veristat

Manages operational start-up and activation activities for multiple clinical studies across country, regional, or global operations. Leads cross-functional teams, ensures compliance with Veristat SOPs, ICH/GCP, and applicable regulations, and oversees efficient study delivery. Provides leadership, mentoring, coaching, and customer-focused communication while managing competing priorities and external stakeholders.

Leads clinical data management activities from study start-up through database lock for complex clinical research projects. Oversees data quality, documentation, project teams, and multiple studies; ensures compliance with SOPs, sponsor requirements, ICH GCP, and regulatory guidelines. Provides technical leadership, mentoring, training, consulting, resource coordination, and expertise in clinical trial databases and EDC systems.

Leads FP&A activities, including forecasting, financial management reporting, profitability analysis, process improvement, and margin enhancement. Manages a finance professional and partners with business and finance leaders across international markets to connect operational outcomes with financial impact. Serves as a strategic advisor, drives transformation, supports KPI performance, and translates growth and efficiency opportunities into actionable plans.

Leads Veristat’s global digital marketing operations and go-to-market execution. Responsibilities include developing and measuring digital strategy, managing global websites and user experience, overseeing HubSpot and Salesforce operations, coordinating contractors, managing social media, tracking analytics, enforcing brand standards, and executing SEO, SEM, email, paid search, A/B testing, personalization, and integrated marketing campaigns.

Leads strategic and operational regulatory consulting for pharmaceutical and biotech clients from early development through NDA/BLA. Prepares IND, NDA/BLA, orphan drug designation, fast-track, and FDA advice-request documentation; advises clients and internal teams; serves as a client and Health Authority liaison; leads FDA interactions; and supports business development and marketing. Provides technical and supervisory leadership while applying knowledge of ICH GCP, clinical trials, regulatory requirements, and CRO-pharmaceutical relationships.

Prepare and compile electronic regulatory submissions (primarily eCTD), collaborate with team members and clients, use MS Word/Adobe Acrobat to format documents, support deadlines, and identify issues with guidance from team leaders.

Administer and maintain Salesforce CRM ensuring data accuracy, manage data health and integrations, enforce data standards, and support workflows.

Lead FP&A team to drive profitable growth across Americas, Europe, and Asia. Own forecasting, financial systems/process improvement, margin and KPI analysis, and translate operational outcomes into financial impact while partnering cross-functionally and advising business leadership.