Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!

Location: Corporate office in Lincoln, NE. Just south of downtown.

As a Bioanalytical Principal Investigator, you will have overall responsibility for the technical conduct of the bioanalytical portion of studies. This role is with our Small Molecule team.

Serve as primary client contact for the bioanalytical segment of studies

Review protocol and assure study is conducted in accordance with Protocol

Document and report any deviations from the protocol to Study Director or Sponsor

Review and approve Sample Analysis Plans

Assure all experimental data is accurately recorded and verified

Assure corrective action is taken and documented when necessary

Review and approve all project-related QA audits

Approve and document any bioanalytical deviations

Review and approve all bioanalytical reports

Assure all study personnel have adequate training, education and experience to perform required study functions

Conduct impact analysis of bioanalytical deviations

Oversight of Event Investigation reports

Minimum of a Bachelor's degree or equivalent in a science-related field with 5 or more years of industry experience preferred

5 or more years of previous laboratory and/or regulated bioanalysis knowledge preferred

Proficiency with computers

Excellent oral and written skills

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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Bioanalytical Principal Investigator - Small Molecule

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