Responsible for project management support to the scientific writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases.
Initiate and amend submission based on comments (as required). Support the writer with internal and external stakeholder communication.
Track the delivery of activities (including managing issues and risks) and support follow up.
Support required submission, compliance/ approval activities, and ensure compliance with publication processes and end-to-end publication management tools (e.g., iEnvision - previously, Datavision/Matrix) and update as required with approval/compliance tools (e.g., PromoMats, DAM).
Support the management of the assigned publication or medical education in line with the agreed budget.
Support and manage as required external spend tracking (e.g., approvals, purchase orders, and goods received).
Support adherence to associated compliance related activities and approvals (with internal stakeholder taking accountability for compliance).
Collaborate effectively with stakeholders: Scientific communication global and/or local teams; and medical content enhancement teams.
Qualification & Experience
Experience: 3-5 years post qualification experience
Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment
Technical skills: Project management; Scientific/Medical writing/communications; Pharma experience (including but not limited to therapeutic area/domain knowledge exposure; and/or publication submission)
Education: University degree level (Graduate degree, preferably in science). Additionally, relevant advanced/postgraduate degree in life sciences/pharmacy/similar discipline desirable