| Area Medical Director | |
| CCM Group Egypt Ref: HP838-05 |
|
The RoleThe RoleReporting directly to MENA VP, the Area Medical Director will have responsibility at the Area level for defining the medical strategy, planning and directing all aspects of an organizations medical policies, programs and staffing. The Medical Director acts as a resource to different stakeholders in enhancing the quality and efficiency of services and processes related to Training, Medico-marketing, Medical Information, Pharmacovigilance, overall Compliance and clinical trials. These activities include the support of, and coordination, with the local Medical Functions, Clinical Research Organizations, consultants, contractors, as well as colleagues in ISMO, Global R&D, Medical Affairs, Regulatory, Compliance and Corporate Legal Affairs. The MENA Medical Director interacts intensely with peers across functions and markets and serve as key link with Global Medical and country organizations in MENA. Effective teamwork is essential. The diversity of the various country organizations requires flexibility and adaptability. Ability to travel extensively through MENA is an indispensable attribute. The Medical Director is also expected to proactively participate in the strategic marketing planning and budget processes for the Area. The position is based at the MENA office in Cairo, Egypt. Duties will include, but not be limited to: Define Area medical strategy/plan in alignment with global strategy. Provides advice, guidance on local medical strategy/plans. Develop and use sound scientific / medical strategies to maximize the potential commercialization of the company products Provide medical support to Area marketing and medical teams at country and MENA level to support their implementation of medical and clinical trial activities Assist in appropriate contribution to development and presentation of operating plans Establish liaisons between company and outside experts to initiate and expedite platform activities; obtains advice and resolves specific issues Ensure strong working relationships and optimal interface with Medical directors /advisors in the direct countries, to drive common understanding of the strategy of medical activities and launches; ensure adequate resources locally (FTEs and clinical research budget) Consequently implement Area projects in accordance with the strategy and plan, in accordance with agreed timelines 1) Product, Business & Opinion Leader Development: Develops regional advocacy for Company products: identifies, develops, maintains and coordinates relationships with regional Brand Advocates, Key Opinion Leaders and main investigators. Support country medical organizations in various interactions with local regulatory authorities, KOLs and other Government Agencies as needed Interact with local and regional Pharma groups and associations when needed Delivers medical & scientific presentations on products during area meetings and regional symposia 2) Medico-marketing: Supervise the proper implementation of medico-marketing activities throughout MENA Partner with Area Marketing function to develop and execute Regional medico-marketing activities, advisory boards meetings, and speakers development programs Support local colleagues in assessing the accuracy of labeling & promotional messages concerning products & competition; 3) Pharmacovigilance Assists the local Medical Directors/Managers in ensuring compliance with applicable local and global regulations for the reporting of adverse events Supervise the development and updating of regional SOPs, and monitor the training plans. Designs and implements methods aiming at the correct and timely reporting of Adverse Drug Reactions across the area, in compliance with the companys Operating Procedures and international guidelines and regulations Provides expertise to subsidiaries and partners in the handling of adverse events and reports. 4) Clinical Research Development, implementation and management of Area and local clinical trials and programs Support pre-activity background research, protocol development and development of other study related documents Effectively present the results of clinical research internally, to external customers, regulatory authorities and other audiences when needed Assist in development, review and approval of country-sponsored clinical protocols |
RequirementsRequirements Medical degree from a reputable University At least 5-7 years in a senior medical function in the pharmaceutical industry Scientific minded personality with record of successful interaction with sales, product & marketing management teams, preferably in multicultural environments Functional experience in most phases of clinical research and in implementation / management of clinical programs Good understanding of international guidelines & regulations relating to drug promotion, and the dissemination of medical information Awareness of competitor activities and external groups working in the same therapeutic area High degree of initiative and ability to work independently Problem solver, articulate and strong advisory skills Strong written and verbal ability; demonstrated proficiency in one-on-one and group presentations Due to the regional scope of this position, you are willing to undertake the associated travel. Fluency in English and French, both written and spoken. |
About the CompanyAbout the CompanyCCM Group was established over 25 years ago to provide professional consulting , publishing and advertising services to help our clients maximize their business potential. CCM Group Specializes in each part of the management puzzle one level at a time. We offer a complete package of management and marketing services to produce profitable solutions. These services include: Advertising, Management and Marketing Consultancy, Recruitment, and Training. |
This Position is closed or expired
|
|
|