Medical Advisor

Major Role Responsibilities:
* Sign-off and approval of marketing materials or activities
* Provision of medical insight and expert opinion as appropriate
* Attendance at meetings requiring medical input, support or representation
* Input and guidance to clinical trial activity and the management of independent research grants and associated budgets
* Reviews and inputs to regulatory documents, strategy and pharmacovigilance matters as appropriate
* Liaises with customers to ensure adequate scientific communication with key opinion leaders and potential users

To provide medical/scientific input into protocol feasibility assessments for clinical trial proposals

To identify appropriate investigators / sites for sponsored clinical trials

To work together with clinical research colleagues and in collaboration with global/EBT WPO and PGRD colleagues to drive the timely completion of sponsored clinical trials

To input into the Global / European Medical Teams to ensure design and selection of trials relevant toUK needs

Medical and Scientific Relations

To provide medical and scientific information to healthcare professionals in response to their specific requests, orally or otherwise, clinical data about marketed products and important scientific information on new products, or those in development

To liaise with healthcare professionals in order to effectively communicate and manage drug safety issues emanating from the region or of a national or international nature

To prepare and/or deliver bespoke presentations to address training and information needs of selected customers e.g. in advisory boards, non-promotional educational symposia for healthcare professionals

To provide medical and scientific input into the organisation sponsored regional and national educational meetings e.g. speaker briefing, agenda selection

Brand and Customer team support

To work with colleagues from brand marketing to adapt and implement reputable and robust promotional materials and meetings based on EBT brand plans

To acquire and maintain in-depth scientific knowledge of the medicines within nominated therapy area(s) (including those in development and in the tail where appropriate) as well as of key competitors.

To provide medical and scientific input into market research activities.

To participate in the training of field-based colleagues on nominated products and competitor intelligence.

To identify, interpret and disseminate new data (safety, clinical trial, publications or SPC changes) to all relevant internal and external stakeholders and highlight new business opportunities.

Compliance

To maintain knowledge of the regulatory environment, the ABPI Code of Practice and the Global Policy on Interactions with Healthcare Professionals (GPIHP) to order to ensure the interests of the patient and the company are protected

If you are intrested in this position please contact Jessica Warden-Brown and send an up to date CV for consideration.

To find out more about Real Staffing please visit www.realstaffing.com