Study Director I Metabolism

Labcorp is a global leader in laboratory services providing the insights and answers that help healthcare providers patients researchers pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science data technology and laboratory network we advance diagnostics accelerate innovation and help address some of the worlds most important health challenges. As we shape the future of healthcare we are leveraging advanced technologies intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise youll have the opportunity to do meaningful work grow your career and make a real impact on peoples health around the world. Together were improving health and improving lives.

Labcorp is seeking a Study Director I Metabolism to join our team in Greenfield IN!

Job Responsibilities:

The Study Director I is responsible for managing the design conduct and reporting of studies to meet scientific regulatory and client requirements in a fast-paced Study Director is the single point of study control and has overall responsibility for the scientific technical and regulatory conduct of studies as well as for the interpretation documentation and reporting of results. Close and regular liaison with the client is of primary importance.

• Coordinate efforts of the study team.

• Learn to develop protocols and ensure that the protocol including any changes is approved and in compliance with appropriate SOPs GLPs and regulatory agency guidelines.

• Ensure that test and control articles are available have been tested for identity etc. and that appropriate technical data are obtained. Also ensure that handling precautions are sufficient to ensure operators safety and that this information is given to the operational areas.

• Learn to review cost estimates to ensure that all protocol/amendment driven work scope specifications are included in the price estimation.

• Understand financial status of ongoing studies.

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

• Direct preparation of reports ensure compliance with protocol and regulatory requirements and submit them to the client.

• Participate in and may host client visits.

Minimum Qualifications:

• Bachelor of science degree with 5 or more years of experience in research or Master of science degree with 2 or more years of experience in research

Preferred Qualifications:

• PhD degree

• 2 or more years of experience with In vivo Pharmacokinetics (PK)

Additional Job Standards:

• Awareness of requirements for working within a GLP GCP and GMP (as appropriate) environment

• Basic awareness of the drug development process regulatory requirements and the scientific techniques of standard metabolism studies required

• Strong client relationship building and management skills

• Ability to communicate effectively verbally and in writing

• Strong attention to detail organization and time management skills

• Skilled in performing scientific presentations and preparing scientific publications

• Experience in a feeder role for a study director with skills and competencies in the relevant study types

• Previous data interpretation and report writing experience

• Working knowledge of MS Word Excel PowerPoint and general IT skills

At Labcorp you can expect the following:

• Innovative Environment: Join a leading healthcare organization committed to driving innovation through internal development to help improve health and improve lives.

• Collaborative Culture: Work in a dynamic inclusive environment that values diverse perspectives and fosters collaboration.

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical Dental Vision Life STD/LTD 401(k) Paid Time Off (PTO) or Flexible Time Off (FTO) Tuition Reimbursement and Employee Stock Purchase regularly scheduled to work less than 20 hours Casual Intern and Temporary employees are only eligible to participate in the 401(k) more detailed information pleaseclick here.

• Relocation assistance available

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging 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 and merit of the individual. Qualified applicants will receive consideration for employment without regard to race religion color national origin sex (including pregnancy childbirth or related medical conditions) 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. Additionally all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

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