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RML, Oncology L20502N00
| Details |
Country: USA
Location: Portland OR
Total applied: 40
Location:US-OR-Portland
Base Pay:N/A
Commission:
$0.00Employee Type:Full-Time Employee
Industry:Pharmaceutical
Manages Others:no |
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RML, Oncology L20502N00
Sanofi-Synthelabo and Aventis Pharmaceuticals, part of the sanofi-aventis Group are facing the future and leading the way as the 3rd largest pharmaceutical company in the world and number 1 in Europe. Backed by a world-class R&D organization, sanofi-aventis is developing leading positions in seven therapeutic areas: cardiovascular disease, thrombosis, oncology, diabetes, central nervous system, internal medicine, and vaccines.Embrace this opportunity to join a diverse and talented group of individuals championed to take on innovation and change in our rapidly expanding organization.Ensure that all activities and interactions comply with Sanofi-Aventis Business guidance's, policies and SOPs, OIG, ACCME, and PhRMA guidelines/policies.. Establish and maintain credible peer-to-peer scientific relationships with international, national, and top regional opinion leaders.. Serve as a primary resource for clinical and scientific information to internal associates and external Health Care providers.. Develop strategic partnerships with scientific and clinical experts based on cutting edge clinical data and information.. Provide timely information on emerging clinical/scientific trends to internal stakeholders.. Provide input in the development of and ensure the appropriate execution of clinically relevant regional medical meetings (e.g. -advisory boards, symposia, consultant and investigator meetings). Ensure delivery of high quality education of new and future product introductions to facilitate optimal patient care.. Collaborate with cross-functional teams in assessing education/research needs and develop education/research strategies to meet those needs.. Critically evaluate the educational quality of company sponsored education programs.. Assist in the identification of Investigators and sites for company trials.. Serve as a liaison for the review, submission, execution and completion of Investigator Initiated Trial proposals.. Collaborate with cross-functional teams to provide balanced and accurate information to top regional formulary decision makers and P&T committee members.. Participate in the spontaneous educational grant process.. Maintain appropriate communication flow with internal and external teams.
REQUIREMENTS
Requirements:. MD, PharmD, PhD (clinical sciences or Healthcare administrative), or Clinical sciences RN, MSN, OCN, PA, NP accompanied by previous pharmaceutical industry or clinical research experience. Knowledge and experience in disease area. Preferred MBA, MHA, MPH, Previous pharmaceutical industry experience. Clear understanding of local medical practice and clinical decision making in regards to patient care. Ability to identify the unmet medical, educational, and research needs within the local medical community. Interpretation of key scientific data and ability to translate this information to meet educational and research needs. Demonstrated ability to address educational and research needs through delivery of cutting edge scientific/evidenced based data.. Understanding of healthcare systems affecting patient care. Understand the design and execution of research studies. Exemplary communication and presentation skills. Ability to think strategically
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