About Predicta Biosciences:

Predicta Biosciences is a seed-stage precision medicine company spun out of the Dana-Farber Cancer Institute. We are supported by a founding team of globally recognized leaders in diagnostics and therapeutics, including Irene Ghobrial, Kenneth Anderson, Gad Getz, Keith Flaherty, and Romanos Pistofidis. Our mission is to develop next-generation blood-based diagnostics for hematologic malignancies, generating rich multi-omics data to power transformative insights. By applying advanced AI and machine learning, we aim to uncover novel therapeutic targets and advance the field of precision oncology.

As we expand our clinical testing capabilities, we are seeking a highly skilled and motivated Clinical Technologist III / Senior Technologist to join our team. With growing sample volume and multiple assay development initiatives in progress, this role is essential to maintaining high-quality testing, regulatory compliance, and operational excellence. The ideal candidate will bring strong technical expertise, thrive in a dynamic startup environment, and play a key role in delivering impactful diagnostic results that drive better patient outcomes.

Key Responsibilities:

· Perform high complexity testing under CLIA regulations, including sample accessioning, cell isolation, cell sorting, NGS workflows, QC, and data review.

· Ensure adherence to laboratory SOPs, regulatory standards, and quality control protocols.

· Participate in assay validation, verification, and documentation of laboratory-developed tests.

· Contribute to the implementation and maintenance of a Quality Management System (QMS).

· Assist in the development and refinement of laboratory procedures and workflows.

· Maintain complete and accurate records in accordance with CLIA and other regulatory standards.

· Participate in internal audits, proficiency testing, and ongoing process improvement initiatives.

· Support efforts toward CAP accreditation through accurate documentation and quality practices.

· Collaborate closely with assay development and data analysis teams to ensure seamless handoff and testing execution.

· Provide training and mentorship to junior technologists as needed.

Qualifications:

· Bachelor’s or Master’s degree in Clinical Laboratory Science, Molecular Biology, Biochemistry, or a related field.

· Minimum of 5 years of hands-on experience in a clinical laboratory setting (CLIA/CAP certified lab).

· Strong working knowledge of molecular diagnostic techniques and regulatory requirements (CLIA, CAP).

· Experience participating in assay validations and implementing quality control measures.

· Detail-oriented with excellent organizational and documentation skills.

· Ability to adapt in a dynamic, startup environment and manage multiple priorities.

· Preferred experience with next-generation sequencing (NGS) workflows or flow cytometry in a clinical or research setting.