Posted to MedZilla on 12/14/2017


Phaidon International

US-IL, Global Medical Affairs Director-Oncology 452431215194-MZ


 
 

Our client is a major pharmaceutical company looking to hire this role immediately at a very flexible and competetive salary.

Relocation is available.

The Global Medical Affairs (GMA) organization provides patients, healthcare providers and payers everywhere with the practical and clinically relevant information and solutions they need to use products safely and effectively, throughout the product lifecycle and the patient’s journey.


Primary Job Function


Provide scientific and technical support for Oncology assigned products; deliver scientific presentations; develops and maintains professional and credible relationships with, key opinion leaders; actively participate in relevant Brand Teams and helps develop medical affairs strategies for assigned products; develop innovative research concepts for clinical data generation; provide relevant scientific and technical training


Key responsibilities:
 

•                   Responsible for compliance with applicable Corporate and Divisional and procedures.


•                   In cooperation with affiliate medical departments, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned products/projects


•                   Establishes and approves scientific methods for hypotheses, rational, design of affiliate protocols and their reports.


•                   Initiates medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy.


•                   Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information.


•                   Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a Oncology therapeutic area resource.


•                   Responsible for understanding the regulatory requirements related to the clinical studies and accountable for complying with those requirements.


•                   Serves as the scientific team interface for key regulatory discussions


•                   May act as medical/scientific leader for projects within an area or across several area


•                   May represent the medical function to the GPT for medical affairs 'activities.


•                   Assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.


•                   Assist with the scientific review, development, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.


•                   May lead cross functional sub teams responsible for discrete projects within the therapeutic area (individual publications or study collaborations)


Initiate research projects and drive them to completion, resulting in high quality publications


•                   Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities


The Global Medical Affairs (GMA) organization provides patients, healthcare providers and payers everywhere with the practical and clinically relevant information and solutions they need to use  products safely and effectively, throughout the product lifecycle and the patient’s journey.

 


Please visit our website at www.phaidoninternational.com

 
 


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