Oversee critical design and analytical aspects of clinical protocols and statistical analysis plans (SAPs).
Oversee strategy and support operational aspects of clinical trial execution, data management and
data analysis in partnership with program operations managers.
Guide content of important clinical and regulatory submissions supporting clinical programs for
all stages of development.
Build and maintain relationships with Key Opinion Leaders and recognized thought leaders.
Lead program specific team meetings/presentations with senior management in US, EU and Japan as
needed.
Evaluate, interpret, and present complex scientific clinical data as required for senior management
on a global basis.
Support regulatory safety reporting for clinical programs: SAE assessment, queries and follow-up, annual reports and investigator brochures.
Draft and review presentations for professional meetings hosted by MDTA on a global basis.
MD or MD/PhD
High level of expertise working under local and international clinical and regulatory requirements for clinical medicine and drug development processes.
Our Value Proposition:
Enjoy the fast-moving, entrepreneurial spirit more typically found in a small biotech, complemented by the benefits of a global pharmaceutical/chemical conglomerate. At this time, Mitsubishi Tanabe Pharma America offers our employees unparalleled opportunities for career success coupled with a supportive level of employee benefits:
Medical/Dental Life Insurance | Supplemental Life Insurance/Dependent Life Insurance |Accidental Death & Dismemberment Insurance | Business Travel Accident Insurance | Short-Term Disability | Long-Term Disability | Flexible Spending Accounts | Employee’s Savings Plan (401K Plan) | Competitive Paid Time Off