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Salary: USD 178,000 - 215,250 / annual
Eikon Therapeutics is a biopharmaceutical company leveraging revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. The company's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), including microscopes that enable real-time, molecular-resolution measurements of protein movement in living cells, unlocking otherwise intractable classes of proteins as drug targets.
You will provide strategic leadership and operational oversight for clinical data management activities, driving the planning, execution, and quality assurance of data management processes while ensuring integrity, accuracy, and compliance throughout the research lifecycle. This is a hybrid role requiring a minimum of 3 days per week onsite in either the Jersey City (NJ) or Millbrae (CA) office.
Key responsibilities include:
- Provide strategic direction and leadership for the clinical data management team, ensuring alignment with company objectives and industry best practices
- Collaborate with cross-functional teams to develop and implement data collection strategies, tools, and systems that meet study goals and regulatory requirements
- Oversee data quality control processes, including validation, discrepancy management, and reconciliation, to ensure accuracy and completeness of collected data
- Lead the design and maintenance of electronic data capture (EDC) systems or databases, ensuring their efficiency and capability to capture essential data elements
- Ensure adherence to data standards, industry best practices, and relevant guidelines throughout the data management lifecycle
- Work closely with biostatisticians, clinical researchers, and regulatory experts to facilitate seamless data integration and analysis
- Ensure all data management activities are conducted in full compliance with applicable regulatory standards and guidelines
- Maintain accurate and comprehensive documentation of data management processes, decisions, and workflows
- Identify and address complex data management challenges proactively, proposing effective solutions to enhance data quality and operational efficiency
- Mentor and develop data management team members, fostering their professional growth and ensuring high performance
Requirements:
- Post-graduate degree with 8+ years of relevant experience, OR Bachelor's degree with 10+ years of relevant experience in Life Sciences, Biostatistics, Computer Science, or a related discipline
- Extensive experience in clinical data management, including data collection, database design, and quality assurance
- In-depth understanding of the biotechnology or pharmaceutical industry and its data management practices, particularly within clinical research
- Proficiency in relevant data management tools and software, including electronic data capture (EDC) systems and data coding standards
- Thorough knowledge of regulatory guidelines related to clinical data management and data integrity
- Demonstrated leadership skills and experience in guiding and mentoring data management teams
- Strong analytical and problem-solving skills, with the ability to address data-related challenges effectively
- Excellent interpersonal and communication skills to collaborate seamlessly with cross-functional teams and external partners
- Oncology experience preferred
- Veeva EDC experience is a plus
