Overview
As Study Director – Ecotoxicology, you lead ecotoxicology studies, ensuring plans align with sponsor goals and regulatory standards. You’ll mentor staff, manage study start-up, and maintain GLP-compliant data and reporting. You will coordinate with sponsors and cross-functional teams to keep studies on schedule and deliver robust findings. This role offers impact in shaping ecotoxicology work for diverse sponsors within Labcorp’s global network.
Pay / Benefits
- Competitive salaries
- No weekend work
- Wider benefits package including pension and generous holiday allowance
Responsibilities
- Lead studies as Study Director/Principal Investigator for ecotoxicology projects across acute and chronic test guidelines
- Prepare, approve and circulate Study Plans; ensure methods meet regulatory/test guideline requirements
- Hold start-up meetings to align staff and mitigate issues before treatment starts
- Ensure test items are properly characterized and hazards/data are identified from literature
- Monitor observations, document responses, and ensure GLP compliance and QA review
- Prepare and finalize concise reports reflecting raw data and study conclusions
- Coordinate data transfer to the Archive per SOPs
- Manage resources (animals, vessels, equipment) for study start-up when needed
- Ensure adherence to the Animals Act and project licences; contribute to department management
- Travel as required to meet sponsors or work in-house to discuss studies
- Provide training, supervision, and mentoring to staff and trainee Study Directors
- Offer advisory support to internal and external customers on study design and regulatory issues
Key requirements
- Significant experience as Study Director in Ecotoxicology
- Working knowledge of GLP and regulatory guidelines
- Skilled in data interpretation and report writing for studies
- Strong customer service communication
- Proficient in project management
- Ability to conduct literature reviews
- Degree in Environmental Sciences or Ecotoxicology
- Strong communication with sponsors and internal teams
- Mentoring and leadership of technical staff
- Problem-solving and proactive planning
- GLP compliance and regulatory guidelines
- Data interpretation and statistical understanding
- Study design and protocol development
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