Eikon Therapeutics Job Trends

Position We are currently recruiting a Senior Manager, Clinical Data Management (Data Management Lead) who will be responsible for timely and high-quality data management deliverables supporting the Eikon portfolio. About You You are a driven individual that focuses on detail.An expert in data management and a strong collaborator. What You’ll Do Provide clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects. Efficiently plan, coordinate, and deliver complete, high quality and reliable clinical trial data in a timely manner for assigned projects. Responsible for end-to-end clinical...

Position We are seeking a highly experienced leader for the role of Executive Director, Clinical Study Management, within the Clinical Operations organization. This individual will lead and manage an expanding global FTE and FSP workforce and will be accountable for the operationally excellent execution of all clinical trials, leveraging internal clinical operations resources to efficiently deliver high-quality clinical data that support regulatory approval of Eikon Therapeutics’ drug candidates across all therapeutic areas. The Head of Clinical Study Management will ensure adherence to Good Clinical Practice (GCP) and to local and global policies and procedures, maintaining inspection readiness and overseeing trial...

Join our Engineering Talent Community Do you thrive on solving complex problems, building innovative technologies, and enabling science through engineering - but don’t see the right role posted today? We’d love to stay connected. By joining our Engineering Talent Community, you’ll have the opportunity to Share your expertise and technical interests with our Talent Acquisition team. Be considered for upcoming opportunities across software, hardware, data, and platform engineering. Stay connected and informed about our Eikon’s growth and progress. If you’re excited about applying engineering to transform biopharma and accelerate innovation, join our community so we can connect as the right...

Join our G&A (Legal, Finance, HR, IT, IS) Talent Community Are you passionate about enabling scientific and clinical innovation through strong business, legal, and operational foundations - but don’t see an open role that matches your background today? We’d still love to connect with you. By joining our G&A Talent Community, you’ll have the opportunity to Share your background in legal, finance, HR, IT, or IS with our Talent Acquisition team. Be considered for future opportunities that support our people, systems, and operations. Stay connected and informed about our Eikon’s growth and progress. If you’re excited about contributing your expertise...

Join Our Research Talent Community Are you passionate about scientific discovery and driving innovation at and away from the bench, but don’t see a current opening that matches your expertise? We’d love to connect with you. By joining our Research Talent Community, you’ll have the opportunity to Share your scientific background and areas of interest with our Talent Acquisition team. Be considered for future research opportunities across discovery and translational science. Stay connected and informed about our Eikon’s growth and progress. If you’re excited about contributing to breakthrough research that fuels clinical development, we encourage you to join our community...

Position We are seeking a highly motivated and skilled Senior Research Associate II with a strong background in stem cell biology and cellular neuroscience to join our Neuroscience research team at Eikon Therapeutics. In this role, you will play a critical part in executing experiments to support target discovery and validation for Parkinson’s Disease. About You You have a Bachelor’s or Master’s degree in Neuroscience, Stem Cell Biology, or a related field, and you are passionate about scientific discovery and exploration. Key Responsibilities Conduct cell culture experiments including utilizing cell lines, primary neuronal cultures, and iPSC-derived cells. Maintain and differentiate...

Position The EHS Specialist 2 is responsible for assisting with planning, implementation, and enforcement of Environmental, Health and Safety (EHS) policies and procedures. The primary objective is to create a healthy, safe, and environmentally friendly workplace, while maintaining compliance to all laws and regulations. This new position will build on programs already in place to support the company as it expands its workforce in numbers and geography, taking ownership of specific programs and collaborating with employees across all departments and levels of the organization. Some of the day-to-day activities for the role include helping to educate employees in the areas...

Position We are seeking a Senior Manager, Regulatory Affairs, to join our dynamic team. In this role, you will play a pivotal part in ensuring that our biotechnological advancements comply with all relevant regulations and standards. You will work closely with cross-functional teams to guide product development and market entry strategies while maintaining compliance and transparency with regulatory agencies. 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 studies and to support...

Position As a Service Technician (Contractor), you will collaborate with automation engineers and operators to help develop and implement corrective actions to maintain robust and reliable performance across multiple equipment and automation system types. You will assist with routine QC and calibrations on our systems and provide daily maintenance documentation and troubleshooting updates. Strong communication and adaptability are essential to success in this position. About You You are someone that is open to working Tuesday through Saturday work schedule (swing shift 230pm – 1100pm). You are able to respond to service requests and repairs equipment as needed. You are a...

Position The Manager, TMF Operations role ensures a complete, accurate and high-quality Trial Master File (TMF) as the subject matter expert through proper, consistent documentation and proactive partner relationship with the clinical study teams. This role will work directly with all functions (internal and external) who contribute to the TMF to ensure regulatory inspection readiness for clinical trials. In addition to ensuring TMF Quality, this role will assist in TMF set-up, document collection and filing, monitoring quality, timeliness, and completeness, and following-up with study teams to resolve TMF-related issues. This role will require a minimum of 3 days a week...