Study Director - Toxicology

Opportunity 

Are you a highly experienced and driven Study Director - Toxicology seeking a new opportunity? Would you like to work for a fast growing global company that prides itself on delivering quality results every time, for every project?  Do you have experience working with clients managing assigned studies from start up to close out? If the answer is yes, then we would like to hear from you.

For candidates based interstate or overseas, relocation assistance to Brisbane, Queensland Australia is on offer and visa sponsorship for you and your family if you are situated overseas.

About you

• Science degree with Honours in an appropriate science qualification (preferably toxicology, pharmacology or pharmaceutical sciences), or an equivalent combination of relevant experience and/or education/training. Ph. D. qualifications highly regarded.
• Minimum 6 years’ relevant work experience, including at least three years’ experience as a Study Director in a GLP-compliant facility undertaking toxicology studies.
• Experience with the design and conduct of rodent toxicology and pharmacokinetics studies.
• Project management experience.
• Proven ability to provide leadership to project teams.
• Experience working in a Quality Systems accredited environment.
• Excellent laboratory skills and high standards of laboratory safety.
• Excellent oral and written communication skills.
• Possess good interpersonal and leadership skills.
• Objective-driven with an understanding of the importance of project timelines and project management.
• Excellent planning, time management and organisational skills.
• Proven ability to deliver tasks on time and with a high degree of accuracy.
• Ability to manage multiple tasks efficiently and adapt to changing priorities.
• Intermediate MS office suite.

In this role you will 

• Act as Study Director in accordance with OECD Consensus Document No.8 “The role and responsibilities of the Study Director in GLP studies”.
• Supervise project staff. 
• Communicate with external clients with regards to projects.
• Design, plan and manage toxicology and pharmacokinetics studies.
• Supporting the application, maintenance and continuous improvement of the Quality Management System and participating in internal and external quality audits as required.
• Ensure all performed studies follow appropriate legal and regulatory regulations.
• Other duties as directed by Line Manager or delegate.

Why Agilex Biolabs

As the leading bioanalytical laboratory for clinical trials, Agilex Biolabs is known globally for its continued investment in the latest technology, and for attracting some of the leading scientists from Australia and around the world. We recognise that our people are our most valuable asset. It is through our employees’ integrity, expertise, and hard work that we can provide high-quality bioanalytical services.

We provide a warm and welcoming work environment for all our employees, we believe that it is critical to the achievement of our organisational objectives that we encourage and maintain a culture which respects, values, and celebrates the wonderful diversity of our people. We promote a collaborative, and fun team environment where you will experience:

• Honest and open communication
• Collaborative teamwork
• Supportive and caring environment
• Mutual respect
• Training & development opportunities
• Flexibility and work-life balance
• A culture which respects and values it's employees.

How to apply

To join our team, please submit your CV along with a cover letter outlining your skills and experience - please submit as one word or PDF document.

                                  www.agilexbiolabs.com