External Research Opportunity Lead > Anderlecht > Joboolo BE :
Société : UCB Lieu : Anderlecht Brussels Site source : Talent BE
Once a study is endorsed, you will develop the research agreement, with careful consideration for the appropriate contracting terms and deliverables (e.g., intellectual property, ownership and use of study results, data privacy, data security, pharmacovigilance requirements, etc.) and coordinate with key internal experts where needed.
You will be responsible for ongoing support of approved studies (e.g., provision of product, milestone tracking, study updates) and communicating updates to the relevant stakeholders.
Who you’ll work withThis role is part of the Global Medical Affairs team and requires collaboration with cross-functional stakeholders from Medical Affairs, Legal, Ethics and Compliance, Patient Safety, and other functions.
In addition, you will interface with the externalresearch party, including investigators and contracting teams.What you’ll doDrive the review and approval activities for externalresearch opportunities, including investigator-initiated studies and research collaborations.Lead review committee meetings for the review, endorsement, and management of studies.Lead the development and negotiation of research agreements, with cross functional input (medical, clinical, legal, etc.).
Provide oversight on compliance to the terms of the contract and progress of the research according to the agreed milestones and facilitate the provision of drug supply where applicable.
Liaise with internal and external stakeholders to ensure timely communication of study progress and delays.
Contribute to the development and refinement of the ExternalResearchOpportunity framework, process and system to ensure a robust and compliant process for review and management of externalresearch studies.
Interested? For this role we’re looking for the following education, experience and skillsMaster’s degree (in the biomedical sciences or equivalent by experience).5+ years of experience within the Pharma/Biotech industry, Academia, Research Institutions or Contract Research Organizations (CRO).3+ experience in managing contracts and its lifecycle (from draft to execution) and partnership oversight.
Demonstrated understanding of the legal and regulatory guidelines associated with pharmaceutical industry research and associated fundings, and the ability to use knowledge to make sound operational decisions.Demonstrated ability to develop trustful relationships with external and internal stakeholders, and leading cross-functional teams to accelerate delivery of qualitative and optimized outcome.Proven skills in negotiation, influencing without authority, managing through ambiguity, and working diplomatically through conflict.Able to work independently in a fast-paced, rapidly changing environment on multiple projects efficiently.Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you! UCB AnderlechtBrussels
