About Us: Careers

Your Career With Pierian Biosciences

Join the Team that is Transforming Cancer Treatment

Pierian Biosciences is looking for the following new team members:

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Head of Quality – Franklin, TN

The Head of Quality has primary accountability for the development and continuous improvement of Pierian’s’ global Quality System to ensure that these procedures, policies, processes, and systems meet the needs of the company’s global business. These needs include regulatory compliance, effective quality management, operational scalability, and the flexibility required by our rapidly growing business.


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Lead Medical Science Liaison

The Lead Medical Science Liaison (MSL) will be responsible for scientific exchange with Key Opinion Leaders (KOLs), pharmaceutical development executives and the National Clinical Trials Network (NCTN) group leads, education of health care providers on DiaTech Holdings (DTH) products, disease states of interest, and facilitation of regional clinical research development, including tissue sample collection procedures and clinical support.


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Scientist/Senior Scientist ImmunoINTEL – Franklin, TN

Under the direction of an assigned Director or Vice President (VP), the Scientist will perform all required Immuno Oncology assay development experiments and process improvement activities in accordance with established procedures to meet all Good Laboratory Practices (GLP) regulatory requirements set forth in the FDA guidelines. She/he will work closely with manufacturing, clinical, and quality staff to foster a team atmosphere striving for continued technical innovations, process improvement and centers of excellence.


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Director of Clinical Operations

The Director of Clinical Operations will have key responsibilities to build the clinical operations team and direct and manage all aspects of the clinical operations program in coordination with other leadership within the company. This includes strategic and operational leadership relative to the direction, planning, execution, and interpretation of clinical programs and the data collection activities.


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Research Associate ChemoINTEL – Franklin, TN

Under the direction of an assigned Director or Scientist, the Research Associate will perform all required assay development experiments and process improvement activities in accordance with established procedures to meet all Good Laboratory Practices (GLP) regulatory requirements set forth in the FDA guidelines. She/he will work closely with development, manufacturing, clinical, and quality staff to foster a team atmosphere striving for continued technical innovations, process improvement and centers of excellence.


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Computational Scientist

This is a Field Position.
In this role, you will collaborate with multiple functional areas to make significant contributions to Pierian’s research, development and clinical programs by bringing your computation expertise to bear on development and application of state of the art proteomics platforms to the creation of clinically actionable information in oncology.


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Lead Clinical Research Associate

The Lead Clinical Research Associate (CRA) reports to and works closely with the Director of Clinical Operations to provide leadership to CRAs in study start-up activities, implementation, monitoring, and close-out activities of multiple clinical trials and process-improvement activities. The Lead CRA works with clinical leadership, vendors, and CRA teams to assure that protocol requirements, bio specimen collection procedures, regulatory guidelines and study timelines are defined and met.


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Manufacturing Services and Technology Quality Assurance Scientist (MSAT-Quality Assurance Scientist)

The Manufacturing Services and Technology Quality Assurance Scientist (MSAT-Quality Assurance Scientist) is part of a team that is responsible for the transition of products from development (verification and validation phase) to manufacturing.  This role will work with the MSAT team to develop quality plans, manufacturing procedures and process validation protocols.  Additional responsibilities include material management, with focus on establishing quality requirements and required verification testing for raw materials through final product as well as product and processes risk management. He/She will contribute to appropriate procedural or troubleshooting references for the operation of equipment, and execute experiments to improve process control and process capability on new and existing processes.  The MSAT QA Scientist will interface with all functional areas such as Research and Development, Quality, and Operations.


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