Study Director - Toxicology

Client Description: Our client?s enabling drug discovery and development technology allows customers to prioritize drug targets, identify biomarkers, and predict toxicity.

Opportunity Statement:

The Study Director ? Toxicology shall serve as the Study Director for preclinical toxicology studies and will be the primary point of contact with sponsors to deliver quality studies on time.

Responsibilities:

Position responsibilities will include, but not limited to;

Client Acquisition
? Overall study oversight and management including technical conduct of the study, interpretation, documentation and reporting of results.
? Primary point of contact with Sponsor on all study related issues.
? Prepare study protocols and amendments, obtain appropriate signatures, arrange for distribution and QA audit, if required.
? Submit IACUC review form.
? Arrange for the required amount of test articles to be delivered
in accordance with SOPs, review and approve study events, i.e., animal orders, formulation procedures, randomization, and any specialized data collection forms.
? Arrange and conduct study pre-initiation meetings.
? Periodically observe animals, critical phases and review study data for scientific quality, animal welfare and compliance with protocol, SOPs and applicable regulations.
? Monitor study budget and time line.
? Respond to QA audits.
? Oversee reporting writing process including writing summary, results, and conclusions, reviewing drafts, receiving and addressing client comments, interacting with contributing scientists as necessary, and approving the final report

Qualifications

Education/Certifications
Ph.D. degree in Pharmacology/Toxicology or related field, or DVM. 
DABT or working toward certification

Professional Qualifications
Our client is seeking an acknowledged, successful, professional with at least 5 years relevant experience in toxicology.
? Expertise in reproductive or developmental toxicology is required.

Characteristics:

? Demonstrated influencing and negotiating ability.
? Self-starter.
? Excellent attention to detail.
? Passion, energy, personal drive and motivation.
? Outstanding written, oral, organizational, and interpersonal skills, are required. 

As a professional search firm, we will only be responding to those inquiries that most
closely align with the stated requirements. Moreover, our client employer can only
review candidates with valid US work authorization at this time. Please include the
position ID (CC 743) in the subject line of your correspondence to ensure review and
forward your credentials (*Word format please), in confidence, to: