Job Description
Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position
We are seeking a highly skilled and motivated Manager, Statistical Programming, to join our dynamic team. In this role, you will play a crucial part in our mission to develop innovative solutions that bridge the gap between biology and technology. As a Manager of Statistical Programming, you will be responsible for statistical analysis and programming activities, ensuring the integrity and accuracy of data-driven insights that drive our research and development efforts.
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 possess significant experience in statistical programming within the biotechnology, pharmaceutical, or healthcare industry, proficiency in programming languages commonly used in statistical analysis (e.g., SAS, R, Python), and strong leadership and team management skills. You demonstrate excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams, as well as knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards for statistical programming. You have demonstrated problem-solving abilities, attention to detail, ability to adapt to a fast-paced and dynamic work environment, and commitment to maintaining the highest standards of data quality and integrity.
What You’ll Do
Statistical Analysis: Collaborate with cross-functional teams to design, develop, and implement statistical analyses and programming solutions for research studies, clinical trials, and experimental data.
Data Integrity: Ensure the quality and integrity of data by implementing rigorous data review processes and adherence to industry standards and regulatory requirements.
Programming: Oversee and review programming activities, including the creation and validation of analysis datasets, tables, listings, and figures for regulatory submissions and internal decision-making.
Process Improvement: Continuously improve and streamline statistical programming processes, methodologies, and standard operating procedures to enhance efficiency and productivity.
Quality Assurance: Perform quality control and validation checks to maintain the accuracy and consistency of statistical outputs.
Collaboration: Collaborate with cross-functional teams, including biostatistics, clinical operations, data management, and research teams, to ensure alignment and timely delivery of statistical programming deliverables.
Training and Development: Provide training, guidance, and support to team members, fostering their professional growth and development.
Compliance: Ensure compliance with industry standards, regulatory guidelines, and company policies related to statistical programming activities.
Qualifications
Post Graduate degree with 4+ years of experience or a Bachelor's degree with 6+ years of experience in a relevant field (e.g., statistics, biostatistics, computer science, or a related discipline).
Significant experience in statistical programming within the biotechnology, pharmaceutical, or healthcare industry.
Proficiency in programming languages commonly used in statistical analysis (e.g., SAS, R, Python).
SQL programming experience required.
Strong leadership and team management skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
Knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards for statistical programming.
AI or automation experience is a plus.
Demonstrated problem-solving abilities and attention to detail.
Ability to adapt to a fast-paced and dynamic work environment.
Commitment to maintaining the highest standards of data quality and integrity.
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
401k plan with company matching
Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
Mental health and wellness benefits
Weeklong summer and winter holiday shutdowns
Generous paid time off and holiday policies
Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
Enhanced parental leave benefit
Daily subsidized lunch program when on-site
The expected salary range for this role is $143,000 to $156,750 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.