Qualification: B.Pharm / M.Pharm / PhD in Pharma / Biotech with an MBA. PMP certification is an addedadvantage
Job Description:
Last3 to 5 years leading Corporate PMO Function experience
Mustpossess experience of 10-12 years in RD /Regulatory / PM related roles.
Hasknowledge of Setting up work for PMO Function
Knowledgeof project planning, initiation, execution, tracking, monitoring, andfacilitating completion of pharmaceutical product portfolio (Oncology) of thecompany.
Shouldhave experience in leading of Cross Functional Team meetings to track monitorprojects
Shouldhave experience of monitoring resources, revenue and capital costs against theproject budget
Experienceof acting as a single point of contact by developing, maintaining and workingto stakeholder engagement strategies and plans
Should have knowledge to ensure project goals are aligned with organizationalobjectives: Project plan updated real-time utilized by project teams totrack activities.
Require good communication skills (Written and verbal both) along with hands on skillsof excel data management PMO.
Monitoringand accountability for technology transfer.
ThresholdRequirement in the Job role (additional but not mandatory)
Should be familiar with:
Developedmarkets Generic Formulation Development.
CurrentRegulatory Guidance understanding pharma regulations across EU Emerging markets
ProjectManagement Processes.
Experiencein Oncology Therapeutic Area would be an added advantage.