Apsida Life Science pioneers targeted therapies for oncology, seeking a Pharmaceutical Consultant to guide clients through intricate regulatory and commercial challenges. This role anchors our consulting practice, delivering precision insights that accelerate drug development and market entry for emerging biotech entities. The position demands crafting bespoke regulatory strategies for IND and NDA submissions, dissecting clinical data to refine trial protocols, and modeling financial impacts of market access decisions. Daily tasks encompass leading workshops with R&D leaders on adaptive trial methodologies, scrutinizing competitor pipelines via advanced analytics platforms, and negotiating with payers to secure reimbursement frameworks. Collaboration spans cross-functional teams, including our in-house pharmacometricians and external CRO partners, on projects like biosimilar launches and rare disease indications. Candidates must hold a PharmD or PhD in pharmaceutical sciences, backed by 7+ years in regulatory affairs or consulting within biotech. Proficiency in Veeva Vault, SAS for data analysis, and FDA/EMA guidelines is non-negotiable. Prior success in shepherding at least three molecules through pivotal trials sets top performers apart. Success hinges on mastering pharmacoeconomics, wielding predictive modeling tools like TreeAge, and navigating stakeholder dynamics in high-stakes environments. Exceptional candidates exhibit sharp analytical rigor, persuasive communication for C-suite briefings, and adaptability to evolving reimbursement policies. Apsida fosters a collaborative ethos where data-driven curiosity thrives amid flat hierarchies and agile project pods. Professionals engage cutting-edge challenges with mentorship from industry veterans, paving paths to senior advisory roles. We provide competitive compensation aligned with market rates, comprehensive health coverage, generous PTO, and 401(k) matching to support sustained excellence.