Director, US Medical Affairs, Multiple Myeloma
Full Time
Director Level
5+ years
Posted 3 weeks ago
Interested in this position?
Upload your resume and we'll match you with this and other relevant opportunities.
Upload Your ResumeAbout This Role
Provide medical leadership for a novel CELMoD asset and support the overall Multiple Myeloma portfolio of products. This role involves integrated strategic planning within Global Medical Affairs and partnership with various internal organizations to lead the US Medical asset strategy.
Responsibilities
- Oversee the US Medical Affairs strategic asset plan development and tactical execution
- Represent US Medical Affairs as a therapeutic area expert in internal and external venues
- Lead launch readiness activities for key late stage asset(s) entering the market
- Lead/support various Medical Affairs cross-functional working groups
- Collaborate with Medical Affairs field colleagues to define, guide and execute therapeutic regional strategies and tactics
- Provide strategic input into the US publication, content development, scientific communications platform, and medical education strategy
- Responsible for field medical leadership, including driving MSL asset strategy, integrated scientific engagement prioritization, and strategic medical insight collection
- Provide high quality clinical input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, steering committee and advisory board meeting materials, medical information response documents, scientific educational grant requests, compassionate use requests, and patient advocacy grant requests
- Track priority Medical Affairs tactics and performance to goals/budget
- Support investigator-initiated trials, RWE planning, and lifecycle data strategy
Requirements
- Experience in Multiple Myeloma
- Advanced degree in health related field such as MD, PharmD or PhD
- A minimum of 5 years industry experience
- Experience in the conduct of clinical trials in hematology/oncology
- Proficiency in clinical data review and interpretation
- Excellent analytical skills
- Solid experience in translating medical/clinical information into medical affairs strategies
- Excellent oral and written communication skills
- Matrix leadership of cross-functional teams
- Demonstrated customer focus orientation & credibility with customers
- Knowledge/application of data sources, reports and tools for the creation of solid plans
Qualifications
- Advanced degree in health-related field such as MD, PharmD or PhD
- A minimum of 5 years industry experience
Benefits
Dental Insurance
Short-Term Disability
Employee Assistance Programs (EAP)
Supplemental health insurance
Business travel protection
Survivor support
Leaves of absence (medical, personal, parental, caregiver, bereavement, military)
Life Insurance
401K Plan
Accident insurance
Paid volunteer days
Paid national holidays
BMS Living Life Better
Identity theft benefit
Unlimited paid sick time
Paid Time Off (unlimited/160 hours depending on role)
Medical Insurance
Long-Term Disability
Pharmacy Coverage
Legal support
Vision Care
BMS Well-Being Account
Personal liability protection
Summer hours flexibility
Optional holidays
Annual Global Shutdown
Related Searches
Similar Jobs
Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development
Active
Bristol Myers Squibb
·
Madison, NJ
·
$186,110 - $225,519
Genomics
Flow cytometry
Gene expression
Immune profiling
1 week ago
Associate Director, Data Engineering
Active
Bristol Myers Squibb
·
New Brunswick, NJ
·
$169,750 - $205,691
Python
SQL
AWS
Java
+13 more
1 week ago
Manufacturing Specialist, Technical Documentation, Cell Therapy Manufacturing
Active
Bristol Myers Squibb
·
Devens, MA
·
$43,840 - $53,120
SAP
MES
Maximo
DeltaV
+3 more
2 weeks ago
Director, Program Management
Active
Bristol Myers Squibb
·
Brisbane, CA
·
$217,250 - $263,258
3 weeks ago
Senior Manager, Cell Therapy Network Lead Investigator
Active
Bristol Myers Squibb
·
Devens, MA
·
$132,230 - $160,237
Project Management
Root cause analysis
cGMP regulations
Risk Mitigation
+2 more
3 weeks ago