Study Director II - Preclinical Oncology

Labcorp • Greenfield, IN

1d • $90,000 - $100,000

About The Position

We have an excellent career opportunity at Labcorp as a Study Director II-Toxicology with a preclinical oncology focus in Greenfield, IN! Relocation assistance available.
(This position is not eligible for visa sponsorship)
At Labcorp, we advance science, technology and innovation and recognized as one of the most respected companies in the world. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. Join us and discover your extraordinary potential!
Job Summary
The Study Director II has overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results in compliance with appropriate SOPs, GLPs, Home Office License requirements and regulatory agency guidelines. They are the main client contact and advisor for ongoing studies and must develop a full understanding of the Sponsor’s requirements. May also serve as a Principal Investigator for designated phases of multi-site studies, as delegated by the Senior Study Director.

Requirements

• Strong client relationship building and management skills.
• Excellent organizational and time management skills.
• Toxicology background.
• 0-2 years of safety assessment study direction experience and drug development experience.
• Ability to help foster a high professional standard and encourage good staff relationships.
• Ability to understand financial status of ongoing studies.

Nice To Haves

• Experience with tumor-bearing models and/or related imaging techniques (e.g. IVIS, etc.)
• Skilled in performing scientific presentations and preparing scientific publications.
• Board certified in toxicology is desired.
• PhD in toxicology or related subject, DVM or equivalent degree preferred.
• Bachelor of Science or Master of Science with more than 3 years of relevant experience may be substituted for PhD.

Responsibilities

• Coordinates the efforts of the study team.
• Learns to develop protocols and ensures that the protocol, including any changes, is approved and in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines.
• Learns to review cost estimates to ensure that all protocol/amendment driven work scope specifications have been included in the price estimation.
• Understands financial status of ongoing studies.
• 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.
• Directs preparation of reports, ensures compliance with protocol and regulatory requirements, and submits them to the client.
• Participates in and may host client visits.

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 Plan.
• Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees