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RML, Oncology L20301N00
| Details |
Country: USA
Location: Detroit MI
Total applied: 33
Location:US-MI-Detroit
Base Pay:N/A
Commission:
$0.00Employee Type:Full-Time Employee
Industry:Pharmaceutical
Manages Others:no |
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RML, Oncology L20301N00
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 strategicallyTravel: 40-50%
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