/ Hiring

Medical Director (MD) Hematology, GDC 0199

Who We Are

At the Roche Group, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 30 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. The headquarters for Roche pharmaceutical operations in the United States, Genentech has multiple therapies on the market for cancer and other serious illnesses. Please take this opportunity to learn about Genentech, where we believe that our employees are our most important asset and are dedicated to remaining a great place to work.

The Position

As the Medical Director you willbe responsible for the design, implementation, monitoring, analysis, andreporting of studies conducted within the Late Development Oncologyorganization. You will also participate in developing the long-range strategicplans for the molecule or molecules within the area of Oncology.

 

Key Accountabilities:

Assisting in the overall management,planning, evaluation and documentation of projects and studies

Participation in on-going medicinedevelopment activities including:

•  Preparation of regulatory documentsand interaction with global regulatory authorities

•  Monitoring and reviewing incomingdata

•  Analysis, presentation andinterpenetration of on-going studies and published data

•  Interactions with health authoritiesand expert bodies

•  Close collaboration with drugsafety, regulatory affairs, medical affairs and clinical trial operations

•  Participation in the preparation ofabstracts, posters and presentations for scientific meetings and congresses

•  Developing and writing clinical plansand protocols ensuring that they are scientifically sound

 

To be successful in this role, youwill have the following skills and experience:

•  Solid experience in medical research includingwriting clinical study reports and interpreting clinical data

•  Good communication and collaborativeskills with experience at working with cross-functional and external groups,including researchers, clinicians and other stakeholders.

•  Proven track record of delivery ofexperimental or novel studies

Confidence at presenting at internaland external strategy meetings

Who You Are

MD (BoardCertification in Oncology required) with clinical practice experience required andstrong scientific/development competence in the relevant therapeutic areademonstrated by peer reviewed publications or production of clinical expertreports.  Sub specialization in relevant therapeutic area (equivalent toboard eligible or board-certified) is highly desirable.

-         Minimum of 5 years experience in clinical research, at least 3 years must havebeen spent in the pharmaceutical industry. Must have past work experience ofconfirmatory drug development and evidence of having played a significant partin the preparation of international regulatory submissions or work with healthauthorities. Exceptional candidates without this level of filing experience maybe considered on an individual basis. Work with health authorities in outcomesmeasures, presentations, negotiations and submissions are considered to beimportant.

·        Ability to interact effectively in a multifunctional multinational team setting

·        Understanding of the business and regulatory aspects in pharmaceutical drugdevelopment.

·        Able to present to internal and external groups effectively and convincingly.

·        Fluent in verbal and written English

The next step is yours. To apply today, click on the "Apply online" button below.

Genentech is an Equal Opportunity Employer.