Eikon Therapeutics Job Trends

Position The Senior Director, Total Rewards will lead the strategy, design, governance, and execution of Eikon's Total Rewards programs, including compensation, equity, benefits, and recognition. Reporting to the Chief People Officer, this highly visible leader will partner closely with Executive Leadership, the Compensation Committee of the Board of Directors, Finance, Legal, and Human Resources to ensure our programs attract, retain, and motivate exceptional talent while supporting our business strategy, culture, and responsibilities as a newly public company. This is a hands-on leadership role for an experienced Total Rewards leader who can balance strategic thinking with operational excellence. The Senior Director...

Position We are currently seeking an experienced Informatics Engineer to contribute to the design, implementation, and development of our informatics processes and systems in support of all phases of our research pipelines. You will work closely with our scientists and engineers to capture and manage functional requirements, and you will be a core member of a team responsible for building scalable, AI-enabled solutions that fit into our information ecosystem and ensure the integrity of our data architecture. About You You are agile of mind and effectively communicate difficult concepts. You work well within a fast-paced, mission-driven, dynamic environment and possess...

Position We are seeking an experienced Senior Director, Regulatory Affairs, to lead our regulatory strategy and compliance efforts. In this critical role, you will be responsible for ensuring that our biotechnological innovations align with all relevant regulations and standards. You will collaborate with cross-functional teams to guide product development and market entry strategies while maintaining a steadfast commitment to regulatory integrity and transparency. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our Jersey City (NJ) office to ensure effective management, operational excellence and high-performance delivery of clinical...

Position In partnership with the Director of Process Management for Clinical Research & Development, the Senior Clinical Quality Operations Manager (Sr. CQOM) is accountable for the execution of operational quality management and inspection readiness activities across Eikon's clinical development programs, to whom this role reports . The Sr. CQOM oversees clinical quality operations across assigned clinical programs, embedding quality-by-design principles, risk-based quality plans, and vendor oversight into Eikon's clinical trials. In partnership withClinical Quality Assurance (CQA), the CQOM drives disciplined execution of quality plans and operational standards, enabling study teams to beinspection ready. This includesensuring consistent execution of quality-by-design(QBD)principles...

Position We are seeking a skilled and highly motivated Senior Manager, Biostatistics to join our talented team. The successful candidate will contribute their statistical expertise and strategic thinking to the design, execution, and analysis of clinical trials and experimental studies. In collaboration with cross-functional teams, you will lead statistical efforts that facilitate evidence-based conclusions and guide our research and development initiatives. About You The ideal candidate for this role should possess a proven track record of designing and analyzing clinical trials and experimental studies, particularly within the biotechnology, pharmaceutical, or related industries. This candidate excels in leading interdisciplinary teams to...

Position As a Senior Clinical Trial Manager, you will play a pivotal role in leading and overseeing our global clinical trial operations. Operating in a dynamic and collaborative environment, you will provide strategic direction and hands-on management to ensure the successful execution of global clinical trials in multiple regions, contributing to the development of groundbreaking therapies with the potential to transform patient lives. The successful candidate will need minimal oversight, will work closely with cross-functional teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support excellence and world class clinical study...

Position Overview The Senior Scientist, CMC Analytical Lead provides analytical leadership for assigned drug substance and drug product programs from IND-enabling studies through clinical development, registration, and commercial readiness. This role supports phase-appropriate analytical strategy and execution across key CMC activities, including IND-enabling, toxicology, early through late-stage clinical supply, drug substance process development, formulation and drug product development, and manufacturing. Responsibilities include analytical input to method readiness, transfer and validation strategy, release and stability strategy, shelf-life planning, specifications, data interpretation, and regulatory submissions. This role is part of the CMC Analytical group and works closely with CMC, Quality, Regulatory, Supply...