Skip navigation
Unable to save this job. Please try again later.

{msg}

Email this Job to Yourself or a Friend

To begin the application process, please enter your email address.

Company Contact Info

  • Bernards, NJ 07920

Already have an account?

Sign in to apply with your saved resumes.

New to CareerBuilder?

Don't have an account? Continue as a guest!

Sorry, we cannot save or unsave this job right now.

Report this Job

Trust and Site Security Team.

Email Send Failed!

Senior Medical Director, GMA Solid Tumor

Daiichi Sankyo, Inc. • Bernards, NJ

Posted 11 days ago

Job Snapshot

Full-Time
Other Great Industries
Health Care, Pharmaceutical
0

Applicant

How Do You Compare to the Competition?

Get facts about other applicants with a CareerBuilder Account

Job Description

About Daiichi Sankyo Cancer Enterprise
The vision of Daiichi Sankyo Cancer Enterprise is to leverage our world-class, innovative science and push beyond traditional thinking in order to create meaningful treatments for patients with cancer. We are dedicated to transforming science into value for patients, and this sense of obligation informs everything we do. Anchored by our Antibody Drug Conjugate (ADC) and Acute Myeloid Leukemia (AML) Franchises, our cancer pipeline includes more than 20 small molecules, monoclonal antibodies and ADCs stemming from our powerful research engines: our two laboratories for biologic/immuno-oncology and small molecules in Japan, and Plexxikon Inc., our small molecule structure-guided R&D center in Berkeley, CA. Compounds in development include: quizartinib, an oral FLT3 inhibitor, for newly-diagnosed and relapsed/refractory AML with FLT3-ITD mutations; DS-8201, anADCfor HER2-expressing breast cancer and gastric cancer or other HER2-expressing solid tumors; and pexidartinib, an oral CSF-1R inhibitor, for tenosynovial giant cell tumor (TGCT), which is also being explored in a range of solid tumors in combination with the anti-PD1 immunotherapy pembrolizumab. For more information, please visit: www.DSCancerEnterprise.com .

Job Summary:

The Senior Medical Director, GMA Solid Tumor will be the Medical Affairs leader for assigned compound/s and /or project(s) under the leadership of the GMA Franchise head. This position is responsible for the implementation of the strategy and execution of the Global Medical Affairs program/s.

Responsibilities:
  • For assigned compound/indications, work collaboratively across functions, within GPT to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information
  • Lead or co-leads GMA Sub teams within GPT, to gain strategic and planning alignment across regions and functions
  • Manages all operational aspects and drives execution for assigned projects of Global Medical Affairs clinical trials in partnership with global line functions, assigned Clinical Trial Operation teams, and regional/country medical associates.
  • Provides Medical leadership to Medical Study Teams for DSI sponsored GMA trials
  • Leads review of investigator-initiated studies (IIS) and Local/Regional Medical Affairs trials concept sheets, within Global IIS review Committee, for assigned projects(s)
  • Supports medical training, medical education and commercial activities in alignment with the Global Brand Team. Provides medical support for scientific symposium and medical congresses within legal and compliance regulations
  • Collaborates across functions to achieve approval of key scientific communications and medical information documents within legal and compliance regulations
  • Provides medical leadership in interactions with key external stakeholders e.g., leads advisory boards, under supervision of GMA Franchise Head
  • Responsible to efficiently manage budgets and resources for DSI Sponsored and GMA supported activities, in collaboration with GMA Franchise Head
Qualifications
Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.

Education/Experience:
  • MD Required, Advanced knowledge in medical/scientific area (Oncology) required.
  • Minimum of 5 years or pharmaceutical experience at local ,regional and/or Global level
  • Have expert operational knowledge and experience in clinical trial design and all stages of clinical trial conduct (Trial design, Start-up, Execution, Analysis, Reporting)
  • Have an excellent knowledge of current clinical practice in Oncology / Hematology / Endocrinology or other relevant disease area
  • Have strong knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products
  • Have excellent communications skills and ability to convey complex scientific and clinical concepts simply and effectively
Ability to travel at least 30% including domestic and international travel

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 ID: 9055BR
Help us improve CareerBuilder by providing feedback about this job: Report this Job.
CAREERBUILDER TIP
For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.
By applying to a job using CareerBuilder you are agreeing to comply with and be subject to the CareerBuilder Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.