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The Senior Manager of Analytical Development will oversee analytical development and quality control activities, manage documentation, and support regulatory content for CMC initiatives.

The role involves overseeing analytical development and quality control for drug substances, managing a team, and communicating effectively on analytical topics.

The Therapeutic Sales Specialist will drive sales in assigned territory, develop business strategies, engage customers, and ensure compliance with regulations while leveraging scientific expertise.

The MSL/Sr. MSL develops relationships with healthcare professionals, leads scientific exchanges, supports medical affairs, and participates in strategic planning and execution. Requires expertise in therapeutic areas with a focus on rare diseases and cardiology.

The Quality Control Manager ensures compliance with cGMP in analytical labs, reviews analytical data, and manages investigations of test results.

The role involves developing relationships with healthcare professionals, educating them, leading collaborations, and participating in clinical research to advance patient care in rare diseases.

The Director leads access and reimbursement strategies for rare diseases, oversees a team, and collaborates across functions to tackle access challenges and ensure compliance.

Provide legal counsel to Sales, Marketing, and Medical Affairs teams in pharma/biotech, ensuring compliance with healthcare regulations while mitigating risks.

The Associate Director, Biostatistics will lead statistical activities in Medical Affairs, ensuring high-quality deliverables and collaboration with cross-functional teams to support medical insights and regulatory standards.

Lead and build a regional sales force to launch and commercialize Encaleret, achieve sales targets, align with commercial/medical teams, develop marketing/KOL relationships, and coach a high-performing team through launch and post-approval activities.