Manager, Medical Operations, EU West at BridgeBio Pharma in Paris

Job description

Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. What You'll Do As Medical Operations Manager, EU West, you will report to the Medical Director EU West and partner closely with the Medical Advisor EU West to build the operating backbone for the affiliate's three rare-disease launches in achondroplasia, limb-girdle muscular dystrophy, and genetic hypocalcaemia. You will own the planning, logistics, systems, and financial coordination of Medical Affairs activities and coordinate local regulatory, compliance, and LEA (loi d’encadrement des avantages) workflows so that execution is efficient, documented, auditable, and aligned with BridgeBio standards and French requirements. The main focus of this role will be France. Responsibilities Medical operations planning: Translate the France medical strategy into an integrated operational plan, activity calendar, RACI, budget, milestones, risks, and KPI dashboard across the three portfolio programs Activity and event delivery: Manage end-to-end operations for advisory boards, scientific meetings, congresses, medical education, internal training, and field initiatives, including invitations, contracting, fair-market-value checks, travel, venues, purchase orders, invoices, and close-out documentation Regulatory coordination: Serve as the affiliate operational contact for Regulatory Affairs, coordinating local inputs, translations, document readiness, correspondence, regulatory intelligence, product information, and launch-readiness actions with regional or global teams and external partners. Support early or compassionate access workstreams when applicable Compliance and LEA governance: Coordinate activities under the French Law on the Regulation of Benefits (Loi d'Encadrement des Avantages, LEA), including the applicable declaration or authorization workflows for healthcare professional, healthcare organization, patient, and patient-organization engagements; maintain approval evidence, due-diligence records, contracts, and auditable files in partnership with Legal and Compliance French transparency requirements: Support accurate and timely capture, reconciliation, and submission of reportable agreements, remuneration, and benefits in line with French transparency and anti-benefit requirements and applicable industry standards Medical review operations: Administer the review and approval workflow for scientific, educational, and cross-functional materials, including intake, routing, version control, source documentation, expiry management, and compliant archiving External funding and research operations: Coordinate medical grants, sponsorships, donations, investigator-sponsored research, collaborative projects, and other external requests from intake through review, contracting, payment, milestone tracking, and close-out Data privacy and records: Embed privacy-by-design and appropriate consent, retention, access, and data-handling practices into medical activities, particularly for health data, research, surveys, and stakehold