Study Director Developmental & Reproductive Toxicology

Labcorp•Greenfield, WI

About The Position

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. We have an excellent career opportunity for a Study Director II – Developmental and Reproductive Toxicology (DART) to join our dynamic team in Greenfield, IN! Relocation assistance available. This position is not eligible for visa sponsorship. Position Summary: The Study Director serves as the DART Study Director for DART Toxicology Studies, including Embryo-fetal Development, Fertility, Pre-/Postnatal and Juvenile Toxicology Studies as described in the GLPs. They have overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results. Activities also include productive interactions with management, technical staff, global internal and external clients, and study direction staff. Other Essential Responsibilities: Stays current with DART study designs and techniques and suggest ideas for technical development as appropriate. Considered a subject matter expert in one or more of the following: fetal pathology, endocrinology, behavioral toxicity/neurotoxicity, juvenile toxicity. Reviews and confirms external, visceral, and skeletal fetal abnormalities. Train in providing expert consultations to clients on customized DART study designs and study timings according to drug development needs.

Requirements

Ability to maintain current regulatory awareness (domestic and foreign).
Ability to accurately read, record, and communicate information to study direction, supervisor, team members, clients, and vendors.
Ability to thrive as a leader in a matrix management structure; demonstrate a positive attitude and mentor novice team members, technical staff, and cross site personal.
Ability to lead projects with little supervision and directive.
Highly skilled in conducting research, data interpretation, and report writing.
Excellent people skills.
PhD in toxicology or related subject, DVM or equivalent degree preferred.
Masters with 2+ years of relevant scientific experience
Bachelor of Science with 5+ years of relevant scientific experience

Nice To Haves

1-2 years CRO experience
2 years Study Director experience - DART

Responsibilities

Stays current with DART study designs and techniques and suggest ideas for technical development as appropriate.
Considered a subject matter expert in one or more of the following: fetal pathology, endocrinology, behavioral toxicity/neurotoxicity, juvenile toxicity.
Reviews and confirms external, visceral, and skeletal fetal abnormalities.
Train in providing expert consultations to clients on customized DART study designs and study timings according to drug development needs.