Associate Director, AESI Education, Clinical Development Functional Excellence in Remote (Remote) at Daiichi Sankyo

Date Posted: 5/24/2024

Job Snapshot

  • Employee Type:
    Full-Time
  • Experience:
    Not Specified
  • Date Posted:
    5/24/2024
  • Job ID:
    R3298
  • Location
    Basking Ridge,NJ

Job Description

Join a Legacy of Innovation 110 Years and Counting! Company is committed to diversity and inclusion
We are an equal opportunity employer including veterans and people with disabilities
SummaryThe Associate Director, Global Oncology Clinical Development (GOCD) Functional Excellence supports the development and creation of Adverse Events of Special Interest (AESI) educational materials
This role works cross-functionally to collect / update safety and treatment information that is ultimately provided to educate patients and Health Care Providers (HCPs) on the risks of treatment and adverse events related to our developing assets
This role requires project management skills to oversee this complex, cross-functional workstream and to ensure comprehensive planning and optimal execution of plans
Other related assignments may include project management, process improvement, tool generation (checklist, process map, etc.), change management and detailed analyses
The Associate Director, GOCD Functional Excellence must have excellent verbal and written communication skills, strong presentation skills and be comfortable interacting with many different global functional groups, external vendors, as well as leaders
Responsibilities - Development of educational materials: For all ADC compounds in development; compiles, creates and edits AESI information
Updates materials when new information is available
Proactively identifies and facilitate risks, mitigations, resolution, and escalation of issues, tracking and communicating status to stakeholders and cross-functional leadership
Educational materials include, but may not be limited to, patient wallet cards, Healthcare Provider (HCP) pocket guides, patient guides, and training slides
Videos and other multi-media training materials may be developed as needed
- Tracking (version control) of educational materials: Develops, maintains, and monitors a process for tracking and maintaining proper version control of all educational materials
- Accessibility to educational materials: Creates, maintains, and controls a library of educational slides to be used for Investigator Meetings, Site Initiation Visits (SIVs) and other educational needs across assets
Partners with IT to ensure information is available both internally and externally via intranet / internet
- External collaboration: Interacts with external development partners to ensure consistency in materials development
Maintains a shared, collaborative e-workspace for development partners to access educational materials
- Vendor Management: Oversees and monitors vendor activities (translations) including, but not limited to contract negotiations and other SOW maintenance
Partners with RD Procurement to ensure business needs are met through vendor services
Ensures invoices are reviewed and paid in a timely manner
- Additional Non-Project related activities: Aid in identifying and raising opportunities for improvement initiatives, fit-for-use clinical development activities, and innovations in addition to amending best practices, as appropriate and in alignment with stakeholders
Specific project assignments may include support in creating and deploying training materials
The Associate Director, GOCD ensures positive / professional interactions and timely collaboration within and beyond Clinical Development with key stakeholders and supporting functions
Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation
Education Qualifications (from an accredited college or university) - Master's Degree in life sciences, business or related field preferred - Bachelor's Degree in science, engineering or business required and Experience Qualifications - 7 or More Years 7-10 years of relevant project management, process improvement, tools development, business analyses or consulting experience
required and - Prior work experience as a project manager, project lead, or similar role within pharmaceutical drug development desirable
preferred TravelAbility to travel up to 10% Global travel might be required Daiichi Sankyo, Inc
is an equal opportunity/affirmative action employer
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Job Requirements