Search the 12 jobs at Eikon Therapeutics

Design and implement machine learning algorithms to support chemistry and advance drug discovery programs. Work collaboratively with scientists and engineers to deploy machine learning models and optimize algorithms for chemical property prediction and reaction optimization. Develop software solutions for high-content datasets and contribute to the innovative drug discovery process at Eikon Therapeutics.

The Principal Engineer, Data Integration at Eikon Therapeutics will coordinate the adoption of standard data representations of drug discovery metadata across departments and data sources. Responsibilities include defining system architecture, working cross-functionally with senior engineers, staying updated with technology trends, and guiding inter-team interfaces design.

The Associate Director, Clinical Data Management is responsible for leading data management deliverables supporting the Eikon portfolio. This role involves managing data collection requirements, overseeing data quality, leading process improvement initiatives, and collaborating with internal and external stakeholders. The position also entails managing clinical data standards and providing leadership in a fast-paced environment.

Seeking a Manager, Study Start Up expert to drive operational excellence and efficiency of clinical trial execution. Responsibilities include study feasibility, data-driven recommendations, planning, site activation, adherence to standards, and supporting clinical trial team.

Seeking an Associate Director, Biostatistics to lead statistical efforts in clinical trials and experimental studies, collaborate with interdisciplinary teams, and provide guidance to team members. Must possess expertise in statistical programming languages, regulatory guidelines, and communication skills.

Seeking experienced Senior Medical Writer to independently lead authoring and editing of medical and regulatory writing deliverables. Responsible for preparing high-quality documentation supporting clinical portfolio objectives. Must have doctoral-level degree in Life Sciences or equivalent experience, with demonstrated scientific writing acumen and project management skills.

Seeking an experienced Senior Manager, Pharmacovigilance to lead and manage safety data across a portfolio of products. Responsibilities include overseeing safety data collection, ensuring compliance, collaborating cross-functionally, and providing pharmacovigilance expertise for product development.

The Director, Regulatory CMC will be responsible for overseeing the development and execution of regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) aspects of pharmaceutical products. This role involves interacting with regulatory agencies, collaborating with cross-functional teams, and ensuring regulatory compliance.

Seeking an Executive Director, Information Security to lead cybersecurity and compliance efforts, develop and execute information security strategies, oversee cybersecurity measures, enforce security policies, collaborate with teams, provide guidance on compliance initiatives, conduct risk assessments, and foster a culture of security awareness.

Seeking a Senior Manager of Study Start-Up to lead study start-up activities for clinical trials, ensuring efficiency and compliance. Collaborate with cross-functional teams, manage data collection, oversee document submission, and address study start-up challenges. Maintain relationships with sites, vendors, and stakeholders. Ensure regulatory compliance and participate in process improvement initiatives.

Seeking an experienced Senior Engineer, Lab Information Management Systems (LIMS) to design and implement LIMS and data management solutions for a biopharmaceutical company's research pipeline. Responsibilities include system design, implementation, data migration, software administration, and collaboration with cross-functional teams to develop digital architecture roadmap.

Seeking a Manager, Regulatory Submissions Publisher to oversee regulatory submissions publishing process, ensure compliance with industry standards, and lead a team of submissions specialists.