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Job Details

Assoc Medical Director / Medical Director / Senior Medical Director, Tecentriq Lung Cancer

Company: Roche
Location:
Reference: 3096343345
Closing Date: 26 May 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Genentech/Roche is seeking a Medical Director or Senior Medical Director to join the Atezolizumab Lung Cancer development team within Product Development Oncology. The Medical Director will play a role in developing and executing the long-range strategic plans for the molecule, including the design, implementation, monitoring, analysis, and reporting of studies. Atezolizumab (Tecentriq) is a monoclonal antibody designed to interfere with PD-L1. ...

Requirements:

Genentech/Roche is seeking a Medical Director or Senior Medical Director to join the Atezolizumab Lung Cancer development team within Product Development Oncology. The Medical Director will play a role in developing and executing the long-range strategic plans for the molecule, including the design, implementation, monitoring, analysis, and reporting of studies. Atezolizumab (Tecentriq) is a monoclonal antibody designed to interfere with PD-L1. Atezolizumab is approved in previously treated NSCLC and bladder cancer (please include standard language)There are 11 ongoing or planned Phase III studies of atezolizumab across certain kinds of lung, kidney, breast and bladder cancer as well as a wide range of studies investigating atezolizumab in combination with other agents.

Position Responsibilities:

  • Participates in CD strategy development and presents to various internal committees
  • Provides clinical oversight across relevant studies and programs
  • Leads or participates in ongoing CST and relevant sub-team meetings, other interactions and communications
  • 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.
  • Participates 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
  • Contributes clinical science input into the relevant therapeutic/disease area scientific strategy. Helps research and other PD groups to ensure consistency of scientific and late-development strategies with target label claims and corporate goals
  • 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.
  • Maintains the highest standards and levels of scientific and clinical knowledge in the specific therapeutic and disease areas

Who you are

You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
  • M.D. with board certification or eligibility in Oncology or Hematology/Oncology required
  • 3+ years of drug development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry required
  • Extensive experience in the design, conduct, analysis, and reporting of clinical studies, including experience submitting NDAs/BLAs to regulatory authorities in the US and/or Europe
  • Demonstrated leadership of development projects and teams
  • Significant successful interactions with key opinion leaders and investigators
  • An excellent scientific track record demonstrated by publication record in peer reviewed journals
  • Proven ability to effectively work in a cross-functional/matrix environment and successfully leverage internal and external partnerships
  • Outstanding organizational and time management skills
  • Strategic agility; in-depth knowledge and broad experience in the pharmaceutical or biotech industry with ability to bring this to bear in accomplishing strategic goals and objectives
  • Excellent judgment and decision-making skills
  • Strong interpersonal, influencing, presentation, and written and verbal communication skills; able to effectively address all levels within an organization and with external collaborators

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.

If you have a disability and need an accommodation in connection with the on-line application process, please email us at US.Accommodation@roche.com.
EEO is the Law

PAY TRANSPARENCY NONDISCRIMINATION PROVISION
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)

Apply for this job: Assoc Medical Director / Medical Director / Senior Medical Director, Tecentriq Lung Cancer

Contact Information:

Address:  UK Head Office
P.O. Box 8, Welwyn Garden City, Hertfordshire, United Kingdom
AL7 3AY
England
Tel:  +44 1707 36 6000
Fax:  +44 1707 33 8297
Website:  Visit Our Web Site

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