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Job Details

Assistant/Associate Medical Director, Atezolizumab Lung Cancer

Company: Roche
Location:
Reference: 3411483151
Closing Date: 23 Nov 17
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Genentech/Roche is seeking an Assistant or Associate Medical Director to join the Atezolizumab Lung Cancer development team within Product Development Oncology. Atezolizumab (also known as MPDL3280A; anti-PDL1) is an investigational monoclonal antibody designed to interfere with PD-L1. ...

Requirements:

Genentech/Roche is seeking an Assistant or Associate Medical Director to join the Atezolizumab Lung Cancer development team within Product Development Oncology. Atezolizumab (also known as MPDL3280A; anti-PDL1) is an investigational monoclonal antibody designed to interfere with PD-L1. 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.

Roche’s Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II – IIIA) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. The Assistant or Associate Medical Director role involves clinical representation on cross-functional teams responsible for the design, implementation, medical monitoring, data interpreting, reporting and publishing of studies conducted within the program.

Key Accountabilities:

  • Participates in the overall management, planning, evaluation and documentation of projects and studies
  • On-going clinical development activities including:
  • Preparation of regulatory documents and interaction with global regulatory authorities
  • Monitoring and reviewing incoming data
  • Analysis, presentation and interpenetration of on-going studies and published data
  • Interactions with health authorities and expert bodies
  • Close collaboration with drug safety, regulatory affairs, medical affairs and clinical trial operations
  • Participation in the preparation of abstracts, posters and presentations for scientific meetings and congresses
  • Developing and writing clinical plans and protocols ensuring that they are scientifically sound
  • Contributes clinical science input into the relevant therapeutic/disease area scientific strategy
  • Collaborates with a variety of internal and external partners and stakeholders
  • 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.

Position Requirements:

  • M.D. with board certification or eligibility in Oncology or Hematology/Oncology required
  • 2+ years of clinical trial experience in the biotechnology or pharmaceutical industry or an academic institution highly preferred
  • Cancer immunotherapy and/or lung cancer expertise required
  • Successful interactions with key opinion leaders and investigators
  • An excellent scientific track record demonstrated by publications in refereed journals
  • Ability to effectively work in a cross-functional/matrix environment
  • Outstanding organizational and time management skills
  • Excellent judgment and decision-making skills
  • Strong interpersonal, influencing, presentation, and written and verbal communication skills
*LI-gRED-KT 

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: Assistant/Associate Medical Director, Atezolizumab 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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