You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

Here in the ICON Strategic Solutions team, we are in an established partnership with a primary multinational pharmaceutical and biotechnology company to supply a permanent, full-time, UK-basedIn vivo SupportAlliance Manager.

This role will have responsibility for the PK/DMPK studies run at CROs supporting all aspects of planning, study design, execution, and reporting.

You will be the main point of contact for the CRO Study Director and will work closely with the Alliance Management, DMPK and Project Teams

As a member of the Alliance Management team for Clinical Pharmacology Safety Sciences, the successful candidate will have the opportunity to build knowledge and experience across a variety of different functional areas (particularly DMPK and Preclinical Toxicology) and will be responsible for supporting and coordinating a variety of tasks and activities ensuring study delivery to quality and timelines.

These may include:

• Study Monitor
• Animal Welfare and Ethical Review
• Issue resolution and escalation
• Partner Performance
• Process Improvement

Strong experience working in a similar capacity, and residing within the UK (with appropriate right-to-work in the UK already granted, if applicable)

• University degree in scientific and/or business discipline, or equivalent experience
• Experienced in vivo toxicologist with hands on experience of working as an animal technician and/or study director supporting DMPK/PK or preclinical toxicology studies.
• Pharmaceutical industry and/or CRO experience.
• Strong organisation and forward-planning skills, with attention to detail
• Understanding of drug development including preclinical and clinical bioanalysis
• Ability to work with multiple stakeholders at different levels within the organization.
• Understanding of drug development including preclinical toxicology and PK/DMPK in vivo studies.
• Ideally, experience of animal welfare, UK Home Office Regulations and 3Rs principles.