Jobs at Harrow

Creates and manages graphic design assets across Harrow’s pharmaceutical brands, including digital, print, email, social, congress, booth, HCP, and patient materials. Adapts campaigns, translates clinical data into visuals, manages Veeva PromoMats and MLR/PRC reviews, maintains brand standards and asset libraries, coordinates print vendors, supports paid media, and builds and tests email campaigns.

Leads curriculum delivery, field coaching, and certification for Surgical and Retina sales teams. Delivers training on ophthalmic products, procedural selling, perioperative positioning, GPO-context selling, retina workflows, and biosimilar adoption. Coaches sales representatives and district managers, verifies clinical content, and directs Field Trainers. Requires substantial buy-and-bill or procedural product sales experience, training or field leadership experience, and approximately 50% national travel.

Leads Harrow’s enterprise digital marketing strategy across social media, omnichannel campaigns, paid media, websites, SEO, analytics, and content. Manages shared digital intake, agency partnerships, digital KPIs, dashboards, CRM-informed segmentation, field tools, launches, and lifecycle programs. Develops digital marketers and collaborates with commercial operations, sales, thought leaders, and agencies. Ensures digital assets comply with pharmaceutical promotional, privacy, and social-media requirements.

Coordinates marketing operations, including budget reconciliation, contracts, purchase orders, invoices, sponsorships, speaker programs, commercial planning, meeting logistics, newsletters, social media support, print fulfillment, vendor management, and branded merchandise inventory. Partners with Finance, Legal, Compliance, Procurement, HR, vendors, and marketing stakeholders while providing weekly status reporting and maintaining compliance.

Manage marketing platforms and the promotional review cycle (PRC) across branded and compounded portfolios. Coordinate, review, and QC promotional materials in Veeva, lead review meetings, ensure regulatory submissions (2253), maintain audit-ready documentation and trademark logs, improve processes/SOPs, train stakeholders, and manage NDCs/labels for compounded products.