Clinical Data Manager

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, the Production clinical laboratory, and data analytics as well as with external stakeholders such as the biopharma partners and CROs. This is a hybrid position, although fully remote is acceptable. Periodic travel may be required. 

Responsibilities 

• Support clinical data management activities for biopharma partnerships, Foresight-sponsored studies (prospective and retrospective), investigator-initiated trials, and other analytical needs as required.

• Develop and maintain data management documentation, including data management plans, relevant portions of study protocols, case report forms (CRF), and CRF completion guidelines.

• 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 clinical trial conduct and evaluation of MRD test performance.

• Generate and review clinical study dashboards and data summaries for use in tracking study progress, centralized data monitoring, and study reports.

• Design case report forms (CRFs), electronic data capture (EDC), and electronic patient-reported outcomes (ePRO) systems for data collection.

• 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.

Skills and Qualifications

Required

• 3-5 years of experience in clinical data management or a similar …