An Associated Medical Advisor is required for a global pharmaceutical corporation located in the 5th settlement: Qualifications: •Medical doctor degree. •Previous pharma Experience of 5-7 years. •Expertise and previous work on Diabetes and metabolic diseases. •Fluency in English & Arabic. •Excellent Communication skills with ability to prioritize. •Knowledge of drug development process preferred, preferably previous experience or expertise in diabetes and/or osteoporosis. •Interpersonal, organizational and negotiation skills. •Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment. •Excellent teamwork skills. •Clinical research experience •Willing to engage in domestic and international travel to the degree appropriate to support the business of the team. Responsibilities: •Knowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals/customers. •Understand and actively address the unsolicited scientific information needs of external health care professionals according to guidelines above. •Participate in reporting of clinical trial data in Clinical Trial Registry activities. •Consider, review or develop pharmacoepidemiologic (quality of life, cost/effectiveness) and health economic aspects. •Support the planning of symposia, advisory board meetings, and other meetings with health care professionals. •Participate in data analysis, development of scientific data dissemination and preparation of final reports. •Support development of slide sets and publications (abstracts, posters, manuscripts). •Support the creation and review of any scientific information with respect to customer questions or media request in accordance with global compliance policies and procedures. •Provide congress support (e.g., availability to answer questions at exhibits, provide oral and poster presentations, staff medical booth, meet thought leaders, and participate in customer events). •Develop and review labeling modifications in collaboration with regulatory and safety groups. •Participate in risk management planning. •Provide medical expertise to regulatory. •Understand the scientific/medical needs of all TA Program Phase customers (payers, patients, health care providers. •Provide advice and consultation to global business unit with regard to potential markets for development compounds and in-licensed projects or compounds. •Support business development in collaboration with the regulatory and corporate affairs group. •Establish and maintain appropriate collaborations and relationships with external experts, thought leaders, and the general medical community on a national and possibly international basis. •Develop and maintain appropriate collaborations and relationships with relevant professional societies. •Participate in patent development. •Critically read and evaluate the relevant medical literature; know the status and data in medical field of interest; and keep updated with medical and other scientific developments relevant to the therapeutic area. •Provide consultation to health outcomes staff, marketing professionals, and management regarding the potential medical need served by (Insert therapeutic area(s), e.g. cardiovascular, cardiometabolic diseases, diabetes mellitus, obesity, etc.) drug candidates. •Knowledge of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the development projects. •Explore and take advantage of opportunities for extramural scientific experiences. •Attend scientific symposia. •Understand and keep updated with the pre-clinical, clinical pharmacology and clinical data relevant to the molecule. •Maintain awareness of current clinical practices through experience or contacts. •Actively set and meet individual professional development goals and contribute to the development of others by being an active source of coaching and feedback to co-workers. •Actively participate in recruitment, diversity, and retention efforts. •Model the leadership behaviors outlined in the ‘On Leadership’ White Paper. •Be an ambassador for the Brand. Interested applicants are required to send their CVs to apply@smartmea quoting “Medical Advisor FB” in the e-mail subject.
Posted on: Sun, 14 Dec 2014 08:00:01 +0000
Trending Topics
Recently Viewed Topics
© 2015