maryland | Associate Medical Director/Medical Director in Laurel, MD

Associate Medical Director/Medical Director

  • F. Hoffmann-La Roche Gruppe
  • $114,840.00 - 169,230.00 / Year *
  • 7200 Spring Valley Rd
  • Laurel, MD 20707
  • Full-Time
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A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Associate Medical Director/Medical Director
United States of America, California, California
Switzerland, Basel-City, Basel
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OVERVIEW:
* Collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in PD, research, business development, commercial operations, legal, etc.
* Represents CD for the assigned molecule(s)/indication(s) to other internal Roche groups
* Develops and provides clinical science information for inclusion into annual and strategic Lifecycle Plans (LCPs) and the Integrated Development Commercialization Plan (IDCP)
* Provides clinical oversight across all relevant studies and programs:
* Leads and/or otherwise participates in ongoing CST and relevant sub-team meetings, other interactions and communications
* Collaborates with relevant teams and other groups to measure and monitor study progress against objectives and plans, including any variances, and proactively communicate any issues, challenges and potential strategies to resolve such
* Plays a lead role in the development and implementation of communications strategies to support existing and concluded studies. Includes KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials
* Works with regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Supports others with clinical science information and input for regulatory submissions and other regulatory processes. Includes developing labeling and packaging language, etc.
Qualifications/Experience
* M.D degree with board certification or eligibility in Oncology or Hematology/Oncology
* Solid tumor experience, preferably in breast cancer.
* Expertise, interest and/or experience in cancer immunotherapy
Abilities:
* Clinical leadership: is respected by others, can effectively contribute to longer-range drug development, and can lead cross-functional teams to successful results
* Confident and competent when interacting with varying levels of internal/external management, KOLs, etc.: stays focused and on-point, is able to raise problems or challenges in a productive and mature manner
* Proven track record of effective decision-making: makes good business decisions and exercises sound judgment. Consistently and effectively balances decisions with imperatives for ethics and efficacy
* Strong orientation to teamwork
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* Who we are
A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.
Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.
* Job facts
+ Location United States of America, California, California | Switzerland, Basel-City, Basel
+ Function Research & Development
+ Subfunction Clinical Operations
+ Schedule Full time
+ Job level Individual contributor
+ Job type Regular
+ Division Roche Pharmaceuticals
+ Posted since 2019/01/24
+ Job-ID 201###-####21
* Get in touch
Ms. Kristy McDill

* M.D degree with board certification or eligibility in Oncology or Hematology/Oncology * Solid tumor experience, preferably in breast cancer. * Expertise, interest and/or experience in cancer immunotherapy Abilities: * Clinical leadership: is respected by others, can effectively contribute to longer-range drug development, and can lead cross-functional teams to successful results * Confident and competent when interacting with varying levels of internal/external management, KOLs, etc.: stays focused and on-point, is able to raise problems or challenges in a productive and mature manner * Proven track record of effective decision-making: makes good business decisions and exercises sound judgment. Consistently and effectively balances decisions with imperatives for ethics and efficacy * Strong orientation to teamwork


Associated topics: ancmg, aoa, breast, cancer, hem onc, hematology, lah, physician md do, radiation, thedacare


* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.