Job description
Location: Remote, Hybrid, or On-Site in Boulder, CO
About Our Company
Foresight Diagnostics is an early-stage, venture-backed molecular diagnostics company that is developing non-invasive cancer detection technologies to improve the lives of patients worldwide. Our portfolio of cell-free DNA based liquid biopsy tests are rooted in novel and proprietary methods developed at Stanford University. Our approach enables the earlier detection of smaller tumors, leading to more personalized and effective cancer treatment strategies for patients. We have deep expertise in molecular biology, bioinformatics, and Next Generation Sequencing (NGS), and maintain a dynamic, fast-paced work environment with significant opportunities for high-impact contribution and rapid professional growth. Foresight Diagnostics is headquartered in Boulder, Colorado.
About The Role
This role will support the planning and execution of clinical trials, including biopharma partnerships and Foresight-sponsored studies. This role will work collaboratively with Medical Affairs, Quality Assurance, Regulatory Affairs, and Production as well as with external stakeholders such as the biopharma partners and CROs. This role will be heavily focused on programmatic aggregation of laboratory and clinical data, data visualization, data cleaning and query reconciliation, and clinical data infrastructure. There will be little to no work with electronic data capture systems (e.g. EDCs, ePROs).
What You Will Do
Support clinical data management activities for biopharma partnerships, Foresight-sponsored studies (prospective and retrospective), investigator-initiated trials, and other projects requiring data support.
Develop and maintain data management documentation, including data management plans and relevant portions of study protocols.
Develop data transfer file requirements and templates for exchange of clinical data, MRD testing data, and biospecimen manifests.
Perform data cleaning activities, including discrepancy management and query resolution for prospective data collection and dataset for retrospective studies.
Data aggregation and internal database development for storage of laboratory and testing data related to IDE/IVD trial conduct
Generate and review clinical study dashboards and data summaries for use in tracking study progress, centralized data monitoring, and study reports.
Conduct data validation checks and implement quality control measures to ensure accuracy and completeness.
Develop and execute standard operating procedures (SOPs) for approval, data entry screen design and testing, validation check testing and approval.
Collaborate with study team members to resolve data-related issues and discrepancies.
Ensure compliance with guidelines, Good Clinical Practice (GCP), CDISC standards and other relevant regulations.
Contribute to the development and validation of data management software tools.
What You Will Bring
Required
3-5 years of experience in clinical data management or a similar role in the pharmaceutical or clinical research industry
Strong understanding of clinical trial processes, data management principles and regulatory guidelines.
Proficiency in electronic data capture (EDC) systems and clinical data management software.
Familiarity with relevant regulations and guidelines, like GCP and CDISC standards.
Knowledge of industry-standard data analysis and reporting software, such as SAS and SQL.
Excellent attention to detail with problem-solving and analytical skills.
Strong organizational and time management abilities.
Preferred
Experience in molecular diagnostics and oncology.
Certification in clinical data management (like CCDM).
Knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM).
Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
Understanding of data privacy and protection regulations (e.g., GDPR).
Effective communication and interpersonal skills to collaborate with other teams.
Proficiency in programming tools such as R (and ecosystem tools like R markdowns and notebooks), or Python (jupyter notebooks)
Proficiency in business intelligence tools, data visualization, and other tools used for data driven decision making.
This role is hiring at an annual salary of $105,000 - $130,000 and is eligible for equity offerings.
Foresight offers benefits including paid vacation, sick time, and parental leave (if applicable), alongside medical, dental, vision, life, disability coverage, flexible spending accounts, and a 401k with company match.
The application deadline for this position is June 30, 2025.
You will be working on interesting problems with extremely high impact. We promote the professional development of our employees and will encourage upward mobility within the company for high performing employees. Foresight Diagnostics is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
