Job Description

This is a supervisor position providing functional and leadership support for scientific writing, data management and data/document migration activities for clinical development sciences team (CDS). This position will support scientific processes that drive quality and timely delivery, as well develop capabilities that align with global CDS priorities.

This position will closely collaborate and communicate with global R&D functions.

Functions, Duties, Tasks:

• Responsible for overall planning and execution of scientific writing/data management/ data migration projects (R&D and Regulatory) to be delivered out of IAC (Innovation & Alliance Centre) ensuring quality, speed and value.

• Run metrics for key performance indicators.
• Responsible for high level of team engagement and provide leadership to the team.
• Foster staff career growth and development by providing timely and constructive feedback.
• Build partnerships across R&D to identify value propositions for CDS IAC.

• Represent CDS IAC and collaborate with the quality organisation for site level quality initiatives as well as corporate level audits and inspections.

• Be up to speed with current industry standards on scientific writing, dossier submission and animal health regulatory guidance.
• Demonstrate high levels of adaptability, flexibility, and learning agility.
• Provide data in a timely fashion to ensure accurate tracking of project budgets and timelines.
• Ensure appropriate levels of quality control, scientific integrity and animal welfare in all activities.
• Supervise resources including new hires, performance issues, terminations, and contractors.

Work with global leader in animal health. |Opportunity to work with one of the fastest growing organization in the industry

Minimum Qualification (education, experience and/or training, required certifications):

• Advanced degree in life sciences, veterinary medicine, biochemistry, pharmacology.

• Minimum 12-15 years of scientific writing or relevant experience in the clinical domain.
• Fundamental understanding of basic data management procedures as well as document repository systems, e.g., Veeva, and SharePoint
• Strong GXP knowledge, in particular GLP, GCP and GMP.
• Good written and verbal communication skills.

• Good people management skills.

Additional Preferences:

• Ability to solve complex problems.
• Sound understanding of operational Regulatory and R&D principles.
• Ability to communicate logically and technically.
• Organisational planning skills, ability to manage competing priorities and flexibility to change.
• Ability to work additional hours as required and work with staff in irregular time zones.

Global leaders in animal health dedicated to innovating and delivering products and services to prevent and treat disease in farm animals. It is an American pharmaceutical company which produces medicines and vaccinations for pets and livestock.

• You will be part of the clinical development sciences team.
• You will work with groups in the USA, Australia, and EU region.
• You will manage company\'s operational requirements locally and ensure implementation of policies and procedures.
• You will be required to directly interact with stakeholders that are on global scientific teams.

Michael Page