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- Tasks: Lead and coordinate preclinical studies, ensuring compliance and scientific integrity.
- Company: Join a dynamic team focused on developing novel therapies in the pharmaceutical industry.
- Benefits: Competitive salary, opportunity to work with cross-functional teams, and impactful research.
- Why this job: Make a real difference in drug development while working in a collaborative environment.
- Qualifications: PhD in relevant field or Master's with experience; 4+ years in preclinical research required.
- Other info: Ideal for motivated individuals eager to influence the future of medicine.
The predicted salary is between 67000 - 80000 £ per year.
Preclinical Study Director
Permanent
£67,000 – £80,000
As a Preclinical Study Director, you will be responsible for overseeing the planning, execution, and reporting of preclinical studies in compliance with regulatory standards (e.g., GLP). You will lead and coordinate cross-functional teams, ensuring the scientific rigor and integrity of studies aimed at evaluating the safety, pharmacology, and toxicology of novel drug candidates. This role requires strong project management skills, a deep understanding of experimental design, and the ability to communicate complex data to both scientific and non-scientific audiences.
Responsibilities:
- Develop and design preclinical studies (e.g., toxicology, pharmacokinetics, efficacy) in collaboration with scientific teams and regulatory departments.
- Ensure that study protocols are aligned with company goals and comply with GLP and regulatory requirements.
- Serve as the main point of contact and scientific lead for preclinical studies, ensuring smooth coordination with internal teams and external CROs.
- Manage study timelines, budgets, and resources, ensuring that studies are completed on time and within budget.
- Oversee the collection, analysis, and interpretation of preclinical data, ensuring the scientific quality and integrity of results.
- Prepare and review comprehensive study reports, ensuring accuracy, completeness, and adherence to regulatory requirements.
- Lead cross-functional project teams, including toxicologists, pharmacologists, lab technicians, and external collaborators.
- Act as a liaison between the preclinical research team and other departments such as clinical development, regulatory affairs, and quality assurance.
- Ensure all studies are conducted in compliance with Good Laboratory Practice (GLP) regulations and other relevant regulatory guidelines.
What we’re looking for:
- PhD in Pharmacology, Biology, or related scientific field (Master’s degree with significant relevant experience may be considered).
- Minimum of 4 years of experience in preclinical research within the pharmaceutical or biotechnology industry.
- Experience in designing, executing, and interpreting preclinical toxicology or pharmacology studies.
- Strong scientific knowledge in pharmacology, toxicology, or related disciplines.
- Excellent project management skills with the ability to manage multiple studies simultaneously.
This position is ideal for a driven and scientifically motivated individual seeking to make a significant impact in the development of novel therapies through preclinical research.#J-18808-Ljbffr
Preclinical Study Director employer: S3 Science
Contact Detail:
S3 Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Preclinical Study Director
✨Tip Number 1
Familiarize yourself with the latest regulatory standards, especially GLP guidelines. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance and quality in preclinical research.
✨Tip Number 2
Network with professionals in the pharmaceutical and biotechnology industries. Attend relevant conferences or webinars where you can meet potential colleagues and learn about current trends in preclinical studies.
✨Tip Number 3
Prepare to discuss specific examples of your project management experience. Be ready to explain how you've successfully managed timelines, budgets, and resources in previous roles, as this is crucial for the Preclinical Study Director position.
✨Tip Number 4
Brush up on your communication skills, particularly in conveying complex scientific data to diverse audiences. Being able to articulate your findings clearly will set you apart as a candidate who can bridge the gap between scientific and non-scientific stakeholders.
We think you need these skills to ace Preclinical Study Director
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in preclinical research, project management, and any specific studies you've designed or led. Use keywords from the job description to align your skills with what the company is looking for.
Craft a Compelling Cover Letter: In your cover letter, express your passion for preclinical research and how your background aligns with the responsibilities of the Preclinical Study Director role. Mention specific projects or experiences that demonstrate your expertise in pharmacology and toxicology.
Highlight Leadership Experience: Since the role involves leading cross-functional teams, emphasize any leadership roles you've held in previous positions. Discuss how you successfully managed teams and coordinated projects to meet deadlines and budgets.
Showcase Communication Skills: Given the need to communicate complex data to various audiences, provide examples of how you've effectively communicated scientific findings to both scientific and non-scientific stakeholders in your past roles.
How to prepare for a job interview at S3 Science
✨Showcase Your Scientific Expertise
Be prepared to discuss your PhD research and any relevant experience in pharmacology or toxicology. Highlight specific studies you've designed or led, emphasizing your understanding of experimental design and regulatory compliance.
✨Demonstrate Project Management Skills
Share examples of how you've successfully managed timelines, budgets, and resources in previous roles. Discuss any tools or methodologies you use to keep projects on track and ensure effective communication within cross-functional teams.
✨Communicate Complex Data Effectively
Practice explaining complex scientific concepts in simple terms. Be ready to provide examples of how you've communicated findings to both scientific and non-scientific audiences, showcasing your ability to bridge the gap between different stakeholders.
✨Prepare for Regulatory Questions
Familiarize yourself with Good Laboratory Practice (GLP) regulations and other relevant guidelines. Be ready to discuss how you've ensured compliance in past studies and how you would approach regulatory challenges in this role.
