Clinical Contracts and Logistic Specialist
Your Responsibilities :
This role gives YOU the opportunity to lead key activities to progress YOUR career, the main of these are :
Provides leadership, oversight and manages the governance and activities involved in the contracting and payments of investigator sites, and the importation and distribution of supply to sites
Accountable for drafting and reviewing contract documents within the agreed timelines across the life cycle of a study.
Accountable for acquiring / maintaining an optimal level of knowledge of GSK Legal requirements, tools and systems to effectively manage them and when needed will develop and integrate contract management tools, templates, methods and processes for the engagement with the GSK policies.
Responsible to manage import and export logistical aspects of clinical studies according to GSK operating standards, local requirements and good clinical practice and to ensure that studies receive the support needed to meet timelines.
Responsible for tracking Imports of study supplies and study Medication :
Monitoring and control of Temporary materials and equipment import and export (Control inputs cancellation, policies and guarantees;
presentation and monitoring.)
Basic Qualifications :
We are looking for professionals with these characteristics to achieve our goals :
Bachelor s degree in Business Administration, Industrial Engineering or related careers.
English level : advanced
3+ years of experience in contracts, logistics, procurement or negotiations.
Microsoft Office knowledge (Advanced Excel skills)
However, if you have the following, it would be considered a plus :
Experience in Pharmaceutical industry.
If you feel this is your next career move, please apply up to September 23th.