Acts as Medical Writer on any type of writing project, including projects with multiple deliverables/components.
Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs senior review of all types of medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing
Advisory board engagements
Market Access Program
System daily check, reconciliation, adverse events screening
Drug supply process
RA, QA, Supply Team, Medical Affairs team engagement
KOLs, Nurses, Pharmacist
Generating reports for quality check
Support initial consolidation of Market Access Program, ongoing in Singapore and ensure complete information are captured
Support in generating records to track the trainings, as necessary
Review Safety notification from global clinical trials and MAPs for overdue actions.
Monthly follow up with physician and acknowledgement
Finance deliverables
Payment related to medical team, milestone payments for RWE studies
Medical Information
Quarterly Quality Check - to be done with Medical Info champion
Generate monthly report
Upload info
HCP Metrics
Track digital engagements and HCP interactions weekly for monthly submission
Audit Readiness
Document repository: Managing info on events, real world studies, all relevant documents
Admin related tasks
Manage calendar for medical team meetings, monthly medical governance meetings, team retros, follow up on pending actions/deliverables and any other support for other projects
