Do you have a passion for Scientific troubleshooting? Customer Service? Project Management? Multi-tasking? Attention to Detail? Please keep reading…

Job Overview

As the Study Director/Principal Investigator for Dose Analysis, you will be responsible for the overall responsibility for client interaction and the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results of routine dose analysis studies in compliance with appropriate company standards, GLP and regulatory guidelines specified in the study plans, protocols or work agreements

• Represents the single point of control for research projects.

• Coordinates efforts of the study team.

• Manages client relationships.

• Compiles and communicates study requirements to appropriate study team members.

• Develops protocols and ensures that the protocol and report, including any changes, are approved and in compliance with appropriate SOPs, GXPs, quality agreements, and regulatory agency guidelines.

• Provides relevant information to assure accuracy of forecast and revenue recognition, reviews cost estimates and financial information for accuracy.

• Monitors progress and status of assigned studies.  Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified. 

• Leads efforts with the study team to troubleshoot and solve assay problems, as necessary.

• Reviews reports for scientific accuracy and completeness.

• Provides technical/scientific guidance and leadership to ensure project completion and to other areas of the company.

• Performs post-project analysis of study performance.

• Leads and sponsors client visits.

• Responsible for ensuring that any unforeseen circumstances that may affect the quality and integrity of the study are identified and documented as they occur and corrective action is taken.

• Responds to unscheduled deadlines, client needs, and crises without neglecting other duties.

• Co-authors scientific papers/posters which are published or presented at scientific meetings.

• Assures on-time delivery of high quality data and reports.

• Evaluates data to assure regulatory guidelines and scientific expectations are met.

• On a broad basis, able to apply appropriate chemistry principles, theories, and concepts within the field of discipline.  Applies a working knowledge of related disciplines.

• Trains less experienced staff.

Education:

• PhD in chemistry, or equivalent degree.  Relevant experience may be substituted for education.

Experience:

• 5-6 years previous related job experience required without PhD

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement. 

About Labcorp

Clear and confident health care decisions begin with questions. At Labcorp, we’re constantly in pursuit of answers. With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry, we’re here for you. More than 70,000 employees strong, we serve clients in more than 100 countries. Labcorp (NYSE: LH) reported revenue of $14 billion in FY 2020.

Connections working at Labcorp