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The Senior Associate, Human Resources plays a key role in delivering efficient, accurate, and employee-focused HR partnering across the employee lifecycle. This position supports onboarding and offboarding, HR systems and records administration, leave coordination, payroll preparation, employment verification, purchasing and vendor administration, compliance activities, and employee programs.
The Senior Associate works closely with HR Business Partners, Talent Acquisition, Payroll, IT, Facilities, Finance, and other stakeholders to ensure HR processes are completed accurately and on time while...
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The Director/Sr. Director, Commercial Production Management (CPM) Strategy & Supplier Relationship Management, is accountable for defining and governing the company’s strategy for external Clinical and Commercial Contract Manufacturing Organizations (CMOs). The role provides objective, portfolio-level oversight, converts performance and risk information into strategic priorities, and ensures that CMO partnerships support reliable supply, quality, cost, and business continuity.
This position establishes the CMO governance model, leads business reviews, oversees strategic initiatives and contract performance, provides integrated...
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The Director, Enterprise Applications will serve as the senior technology and business-process leader responsible for the strategy, architecture, delivery, support, and continuous improvement of SK Life Science’s enterprise application portfolio.
This position will partner with business leaders and cross-functional teams to identify and recommend technology solutions; gather and prioritize requirements; plan demand; and lead the design, development, configuration, integration, implementation, validation,...
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The Senior Director, Regulatory Affairs Advertising, Promotion (Ad/Promo), and Labeling is a critical leadership role responsible for developing and executing regulatory strategy for all product communications and core labeling. This leader will ensure that all commercial and non-promotional materials, as well as core and local product labeling, are compliant with US FDA, EMA, and other relevant global regulations. The role requires expert-level interpretation of complex regulatory requirements and a proven ability to lead and influence cross-functional teams to achieve both compliance and business goals.
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The Scientist, Analytical Method Development for Radiopharmaceuticals, is responsible for the development, optimization, validation, and transfer of analytical methods supporting radiopharmaceutical products across early- and late-stage development. This role requires strong technical expertise in analytical chemistry and a solid understanding of the unique challenges associated with radiopharmaceuticals, including short half-life materials, radioactive impurities, and time-critical testing. The position sits within CMC organization and works closely with Quality, Manufacturing, and external partners to ensure robust, compliant, and transferable analytical methods.
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The Senior AI Solutions Engineer brings a track record of building and operating AI services directly, and uses that hands-on foundation to lead AI transformation across Business, Commercial, Supply Chain Management, and Staff functions. The role is part enabler and part builder: it raises what non-technical colleagues can do on their own, and personally leads the projects that go beyond their reach.
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The Clinical Pharmacology (CP) Associate Director role will effectively provide expertise and support for the design, execution, interpretation and reporting of clinical pharmacokinetic/pharmacodynamic (PK/PD) studies. This individual will participate in the selection of Phase 1 CROs for clinical pharmacology studies. Individual will be functional CP Lead will ensure that the preclinical characterization is adequate and provides support in characterizing the clinical pharmacology profile of a given compound; and also ensure that the CP strategy/plans fully support the selection of dose(s) and regimen for Phase 1, 2 and 3 studies. Individual will serve as CP representative on studies and project teams, and will contribute to the...
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The Vice President, Quantitative Sciences & Developmentprovides strategic, scientific, and operational leadership for the company's Clinical Pharmacology, Pharmacometrics, Toxicology, DMPK, Biostatistics, Statistical Programming, and Clinical Data Management functions across all phases of drug development.
This executive is responsible for developing and overseeing execution of integrated quantitative strategies that support efficient translation from...
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- The Neuroscience Account Manager (NAM) is responsible for driving SKLSI product sales within New Brunswick, NJ
- The NAM must demonstrate a strong understanding of the local healthcare marketplace and local payer landscape. The position requires a knowledge of appropriate disease states as well as the ability to communicate necessary technical, scientific and product information to called on Healthcare Professionals (HCPs)
- The NAM must be able to effectively collaborate with field-based...
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The Medical Science Liaison (MSL) will be responsible for providing non-promotional scientific, educational, and research support for the company and their CNS portfolio in the Northeast region which consists of NY, NJ and Eastern PA. The MSL position is a field based member of the Medical /Clinical Affairs team. The MSL should be highly trained in a health care field and well-versed in clinical and for basic science to be able to deliver cutting edge data and technical/practical education to Health Care Professionals (HCP).
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The Director of Inspection Management/Quality Compliance will report to the VP and Head of Global Quality. The Director, GCP/GVP QA, leads the end-to-end GCP/GVP QA strategy, compliance, and inspection readiness program across the organization. The role oversees a GCP QA team, drives risk-based audits and quality-by-design integration, and manages quality risk processes, metrics, and compliance oversight for GCP and GVP activities. Key compliance responsibilities include monitoring adherence to GCP/GVP regulations, company SOPs, and ICH guidelines; assessing and reporting compliance status across functions; and ensuring timely remediation of findings from audits and inspections. The Director also...
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The Medical Science Liaison (MSL) will be responsible for providing non-promotional scientific, educational, and research support for the company and their CNS portfolio in the respective territory. The MSL position is a field based member of the Medical /Clinical Affairs team. The MSL should be highly trained in a health care field and well-versed in clinical and for basic science to be able to deliver cutting edge data and technical/practical education to Health Care Professionals (HCP).
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The AI Engineer, Biz Ops will build the AI‑powered services that form the backbone of our decision‑intelligence platform. In this role, you will take AI models developed by AI Scientists and transform them into scalable, production‑ready applications by designing inference pipelines, APIs, and supporting data flows.
You will work closely with Data Engineers to integrate model pipelines with the broader data ecosystem and collaborate with business operations and commercial teams to convert manual, step-driven workflows into AI‑native services. This includes building reliable batch and real‑time inference systems that generate measurable impact across business operations—not limited to any specific...
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The AI Scientist will design, prototype, and advance next-generation AI systems for clinical development, translational research, and broader pharmaceutical R&D, leveraging and extending AI approaches across the R&D lifecycle.
This role focuses on exploring and applying emerging AI methodologies to advance clinical and translational research, support data-driven decision-making, and improve R&D workflows. Relevant experience may come from clinical development, translational research, drug discovery, computational biology, or other data-intensive areas of pharmaceutical...
