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Alliance Manager In vivo Support

  1. Reading
2024-115013
  1. Medical & Scientific Affairs
  2. ICON Strategic Solutions
  3. Remote

About the role

Alliance Manager Support Specialist (Study Monitor) - Clinical Pharmacology & Safety Sciences (UK, home-based) - Associate Project Manager level

The role will support the successful outsourcing of DMPK studies as a Study Monitor for in vivo PK/DMPK studies.

 

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-based In vivo Support Alliance 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.

Why ICON?

 

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

 

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

 

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

 

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

 

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