Director of Biopharma Partnerships

ph3Responsibilities /h3 ul liThe Hunt: Origination Pipeline Building /li liTargeted Prospecting: Systematically map the global Biopharma landscape (especially in Rare Diseases, Targeted Oncology, and Immunology) to identify active Phase 2b/3 pipelines that are bottlenecked by patient recruitment. /li liEvangelizing the ULAI Dragnet: Secure high‑level meetings with VPs of Clinical Operations, Heads of RWD, and Clinical Development Leaders. Pitch the unique value of our multi‑modal OS infrastructure and prove how we can intercept their exact inclusion/exclusion criteria upstream. /li liNetwork Leverage: Utilize your existing rolodex within Biopharma to fast‑track conversations, bypassing standard procurement layers to engage directly with the clinical decision‑makers feeling the pain of delayed trials. /li liComplex Deal Execution /li liSolution Architecture: Work with Pharma sponsors to define the exact diagnostic footprint required (e.g., combining imaging findings with declining kidney function for rare disease profiles) and translate that into a commercial data/recruitment contract. /li liClosing: Own the end‑to‑end sales cycle. Negotiate complex SaaS, RWD licensing, and milestone‑based clinical recruitment contracts from initial MSA through to final signature. /li liAlliance Management Delivery /li liThe Clinical Bridge: You don't just sell the deal and walk away. You will serve as the Alliance Manager, bridging the gap between the Pharma sponsor's clinical teams and ULAI’s internal engineering and clinical informatics teams. /li liExecution Oversight: Ensure that the data pipelines and screening algorithms we deploy actually yield the patient volumes and RWD quality promised in the contract. /li liAccount Expansion: Once a pilot rare disease dragnet proves successful, leverage that internal Pharma champion to expand ULAI's contracts across their broader therapeutic portfolio. /li /ul h3Requirements /h3 ul liThe Hunter Mentality: You are deeply uncomfortable with an empty calendar. You are relentless, resilient, and view pipeline generation as the most critical part of your day. /li liDomain Fluency: You speak the language of clinical trials, real‑world evidence, and targeted therapeutics. You understand what Phase 2a vs. Phase 3 requires, what a synthetic control arm is, and why recruiting for a rare genetic disease is a nightmare. /li liTrack Record: 5–10+ years of quota‑carrying BD experience selling RWD, complex CRO services, genomic testing, or tech‑enabled clinical trial solutions directly to Biopharma. You have a documented history of closing complex, large‑scale deals. /li liAutonomy Grit: You thrive in a seed‑stage, fast‑moving environment. You do not need a massive marketing department to generate a pitch deck; you build the narrative, find the target, and close the deal. /li liLanguage: Fluent English is mandatory; professional proficiency in French or German is highly advantageous. /li /ul /p #J-18808-Ljbffr