Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.
Overview
Iovance is seeking a Contract Statistical Programmer to support clinical development programs by developing, validating, and maintaining statistical programming deliverables for clinical studies and regulatory submissions. This role will work closely with statisticians, data management, and other cross-functional teams to ensure high-quality and timely delivery of datasets, tables, listings, and figures in a GxP-compliant environment. The ideal candidate combines strong programming expertise with a solid foundation in statistics or quantitative sciences and thrives in a collaborative, fast-paced biotech setting.
Essential Functions and Responsibilities
- Develop, validate, and maintain SAS and/or R programs for the creation of SDTM, ADaM datasets, and TLFs in accordance with CDISC standards.
- Support statistical analyses for periodic safety reports, publications, conference presentations, IDMC/DSMB reviews, clinical study reports (CSRs), regulatory submissions, health authority requests and other ad hoc analyses and reporting needs.
- Ensure all programming activities comply with FDA 21 CFR Part 11, GxP, and internal SOPs.
- Collaborate with biostatisticians, data managers, and clinical teams to define analysis specifications and resolve data issues.
- Perform quality control and detailed review of statistical programs and outputs.
- Develop and maintain reusable macros, templates, and automation tools to improve programming efficiency.
- Contribute to the evaluation and implementation of emerging technologies and modern programming approaches, including AI-based tools and agents, to enhance statistical programming workflows.
- Participate in development and review programming data specifications.
- Maintain clear, thorough documentation to support audit readiness and regulatory inspection.
- Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
- Perform miscellaneous duties as assigned.
Required Education, Skills, and Knowledge
- Master’s degree in mathematics, statistics, computer science, biostatistics, data science or a related quantitative field with 5+ years of relevant industry experience; or bachelor’s degree in mathematics, statistics, computer science, biostatistics, data science or a related quantitative field with 8+ years of relevant industry experience
- Strong proficiency in SAS and/or R for clinical trial data analysis and reporting.
- Working knowledge of CDISC standards (SDTM, ADaM, Define-XML) and regulatory submission requirements.
- Experience producing TLFs and SDTM/analysis datasets in a pharmaceutical, biotechnology, or CRO setting.
- Experience with oncology clinical trials or cell/gene therapy programs.
- Strong analytical, problem-solving, and communication skills.
- Familiarity with regulatory guidelines (FDA, ICH) and GxP-compliant programming practices.
- Excellent attention to detail, problem-solving skills, and the ability to manage multiple priorities independently in a remote environment.
Preferred Education, Skills, and Knowledge
- Master’s degree in mathematics, statistics, or computer science is strongly preferred.
- Hands-on experience developing AI agents or applying AI/ML-based automation tools to streamline data analysis, programming workflows, or reporting processes is a significant plus.
- Experience supporting regulatory submissions (NDA, BLA, MAA, or equivalent)
- Familiarity with electronic submission standards (eCTD) and health authority interactions.
Physical Demands and Activities Required
The physical demands described here represent those an employee may encounter while performing the essential functions of this job. Reasonable accommodation may be provided to enable individuals to perform these functions.
- Ability to remain in a stationary position for extended periods
- Ability to move about within an office or remote workspace and exert up to 10 pounds of force occasionally
- Visual acuity sufficient for preparing and analyzing data, viewing computer screens, and extensive reading
- Repetitive motion involving wrists, hands, and/or fingers
- Ability to communicate effectively to exchange information
- Cognitive: Ability to engage in analytical, conceptual, and problem‑solving activities in a dynamic business environment
Work Environment
This role operates in a professional office or remote work environment and requires routine use of standard office equipment and technology. Employees working remotely are expected to maintain a safe workspace free from recognized hazards.
#LI-remote
The annual base salary we reasonably expect to pay is listed. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of the role, job duties/requirements, and relevant education, experience and skills.
The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.
Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact [email protected].
By voluntarily providing information and clicking “Submit Application”, you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice.
Skills Required
- Master's degree in mathematics, statistics, computer science, biostatistics, data science or related field with 5+ years industry experience OR Bachelor's with 8+ years
- Strong proficiency in SAS and/or R for clinical trial data analysis and reporting
- Working knowledge of CDISC standards (SDTM, ADaM, Define-XML) and regulatory submission requirements
- Experience producing TLFs and SDTM/analysis datasets in a pharmaceutical, biotechnology, or CRO setting
- Familiarity with FDA, ICH guidelines and GxP-compliant programming practices including FDA 21 CFR Part 11
- Experience with oncology clinical trials or cell/gene therapy programs
- Strong analytical, problem-solving, communication skills and attention to detail; ability to manage multiple priorities remotely
- Hands-on experience developing AI agents or applying AI/ML automation tools to programming workflows
- Experience supporting regulatory submissions (NDA, BLA, MAA) and familiarity with electronic submission standards (eCTD)
What We Do
Iovance Biotherapeutics (NASDAQ: IOVA) aims to improve patient care for people living with cancer. Iovance is investigating T cell-based therapies, known as tumor infiltrating lymphocytes (TIL), which use a patient’s own immune cells to attack cancer. Our unique Iovance TIL technology platform has generated novel cell therapies that are currently in clinical studies for multiple cancers. We are adding to our talented team as we actively prepare for our initial commercial launch, advance our research and development efforts, and build our internal manufacturing capabilities. Iovance is headquartered in the San Francisco Bay Area. Our Iovance Cell Therapy Center (iCTC), a state-of-the-art manufacturing facility, is located in Philadelphia. We also have a research site in Tampa, Florida. Any information expressed by Iovance is subject to the risk factors and information on forward-looking statements contained in its filings with the Securities and Exchange Commission and available here: https://ir.iovance.com/sec-filings
