Eikon Therapeutics Job Trends

Position We are seeking a Clinical Scientist that will lead the scientific planning and collaborate with both Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a cross-functional clinical development team. You will be a key contributor in the clinical science activities of evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results. This role will require a minimum of...

Position The Director Study Site Engagement & Monitoring Excellence will be responsible for leading the development and execution of Eikon’s global trial site engagement strategy, including oversight and accountability for all internal/external managed site monitoring activities to ensure predictable delivery of high-quality data and establish Eikon as a preferred sponsor for clinical sites. The Director will ensure effective collaboration with clinical study teams, and Functional Service Provider (FSP) partners, to implement excellent site relationship management and site monitoring activities to accelerate operational excellent delivery of Eikon’s clinical programs. This role will require a minimum of 3 days a week of...

Position We are seeking a seasoned physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician as a Senior Director, Clinical Research, Oncology. In this role, you will play a pivotal part in advancing our Oncology pipeline by providing medical expertise, strategic leadership, and operational oversight for multiple clinical development studies. About You You are a highly accomplished professional who excels in the development and execution of clinical projects. As a key member of the cross-functional Development Teams and the Clinical Study Teams, you will...

Position The Senior Manager, Statistical Programming will be responsible for statistical programming deliverables in Eikon clinical studies. In this role, you will report to the Sr. Director, Statistical Programming. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. About You You have experience with the oversight and management of statistical programming deliverables for clinical studies, ensuring that they meet quality, compliance, and...

Position Eikon Therapeutics is seeking a highly motivated Technician 1, Lab Support to support our dynamic R&D teams. This individual will contribute to efficient laboratory operations by performing a variety of core lab support duties. About You The ideal applicant is organized, able to multi-task across multiple responsibilities, and comfortable working in a fast-paced environment. This role reports to the Lab Manager and involves daily interaction with scientific staff. This is a full-time, non-exempt position working 40 hours per week, Monday–Friday. What You'll Do Transport, clean, and sterilize glassware, plasticware, and laboratory equipment by safely operating an autoclave, commercial dishwasher,...

Position We are currently recruiting a Senior Manager, Clinical Data Management (Data Management Lead) who is responsible for timely and high-quality data management deliverables supporting the Eikon portfolio. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City (NJ) or Millbrae (CA) offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. About You You are a driven individual that focuses on detail.An expert in data management and a strong collaborator....

Position We are seeking a Clinical Scientist Data Reviewer that will support the scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate technical skills and scientific acumen as part of a cross-functional clinical development team. You will be a key contributor and supporter in the clinical science activities of evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results. This role will be focused...

Position We are seeking an Associate Director, Study Start-Up to join our Clinical Operations team. In this role, you will support the Eikon Therapeutics portfolio of studies and lead study, country and site feasibility activities for one or multiple clinical trials, ensuring that study forecasts have a > 80% probability of occurring as planned. You will leverage industry benchmarks and cycle times to perform study, country and site feasibility and forecast study timelines as well as evaluate / improve business processes to accelerate site activation. You will directly engage and influence interactions with Clinicians, Study Management, Investigator Sites and support...

Position We are seeking an experienced, detail-oriented individual to join our Medical Writing team. In the Senior Medical Writer role, you will be responsible for independently leading document development by authoring and editing of medical and regulatory writing deliverables that support the Eikon clinical portfolio. You will partner with cross functional colleagues within study teams/project teams to prepare high-quality, accurate and fit for use clinical and regulatory documents enabling delivery of Eikon portfolio milestones. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City...

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...