Eikon Therapeutics Job Trends

Position We are seeking an accomplished Senior Director, Procurement and Supply Chain, to lead our procurement and supply chain functions. This role is instrumental in overseeing the strategic direction of sourcing, procurement, and supply chain management to support our high-growth biotech operations. About You The ideal candidate for this position holds extensive expertise in procurement, supply chain management, or related leadership roles, preferably within the biotechnology or a related industry, the candidate demonstrates exceptional strategic thinking, analytical prowess, and problem-solving skills. They excel in negotiation, communication, and relationship-building, particularly in negotiating complex contracts, and possess proficiency in Microsoft Office applications,...

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 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...