Director, Clinical Scientist
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POST DATE 9/19/2017
END DATE 11/17/2017
JOB DESCRIPTIONDIRECTOR, CLINICAL SCIENTIST
Do you have the passion to join a young global biopharmaceutical whose sole mission is to improve the lives of patients bravely facing cancer? Does it excite you to be a part of a rapidly expanding company with multiple marketed products and a diverse and robust pipeline? If yes, you may be a great fit for our community of dedicated and innovative associates.
YOUR IMPACT AT TESARO:
The Director, Clinical Scientist will provide scientific support for all Medical Development activities, including assembling, evaluating, and presenting scientific and medical data, writing manuscripts (paper, abstracts, posters, etc.), monitoring the competitive landscape and reviewing and summarizing relevant literature. S/he will clearly communicate concepts and information, both in writing and via formal presentations, to scientific and medical experts, both internal and external to the company. S/he will have a substantial role in the development of clinical documents, the review of scientific and clinical data and the communication of data to the scientific and medical communities. The role will report to a Medical Director and will collaborate with Clinical Pharmacology, Clinical Research and other functions within TESARO.
Study Data Review and Analysis
Perform ongoing review and analysis of study data
Provide support as needed for scientific issues that may arise during study execution
Provide support for publication of data (manuscripts, posters, etc.)
Clinical Study protocols and protocol synopses
Systematically survey public domain for relevant information from competition
Summarize clinical trial designs and data for similar drug products
Review and summarize Summary Basis of Approval documents for competitive compounds
REVIEW OF SCIENTIFIC LITERATURE
Perform literature searches and critically review and summarize the relevant scientific, drug development and medical literature to support document development, such as the investigator brochure, protocol design, clinical study report, competitive assessments, etc.
Provide scientific/medical supportive materials to in-house staff and external consultants in the indications being studied
Identify and review literature that addresses specific topics of interest relevant to TESARO drug candidates
Doctoral level degree preferred. PhD, MD, MSc/MPH, PharmD, with 10 years of experience within a pharmaceutical company environment required
Hematology/oncology disease experience preferred
Excellent management, communication and organizational skills required with demonstrated success in leading projects and interacting with cross-functional teams
Passionate, committed and a strong team player
Ability to work independently and reliably deliver objectives of high quality in a timely manner
Ability to think creatively, function independently, deliver on timelines, have strategic insights and have a detailed knowledge of the activities and procedures involved in clinical drug development.
TESARO is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.