Associate Medical Director, Medical Affairs - Elahere

Job Description
Purpose:
The Associate Medical Director provides specialist medical/scientific strategic and operational input into core medical affairs activities within their TA inclusive of healthcare professional/provider interactions;
generation of clinical and scientific data;
educational initiatives(medical education, data, guidelines and value proposition);
safeguarding patient safety (risk minimization activities / safety surveillance activities). Works closely with commercial colleagues (marketing, market access) to provide strategic medical input into core brand strategies. Provides scientific and technical support for assigned products;
delivers scientific presentations;
develops and maintains professional and credible relationships with key opinion leaders;
actively participates in relevant Brand Teams and helps develop medical affairs strategies for assigned products. Develops innovative research concepts for clinical data generation and provides relevant scientific and technical training.
Responsibilities:
Develops, reviews and follows up on clinical studies and medical projects initiated within the relevant therapeutic area (e.G. post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorization studies (phase IV), IIS projects, etc.) at the regional/local level.
Participation in design and execution of clinical trial safety, product safety and risk management plans. Responsible for routine and adhoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse Events (AE’s) and Serious Adverse Events (SAE’s) if assigned to AbbVie conduct on clinical studies.
May interact with and coordinates appropriate scientific and medical activities with internal stakeholders (i.E. commercial, clinical operations, discovery, statistics, regulatory, etc…) as they relate to on-going medical affairs projects. May assist as consultant/liaison with other corporations when working under licensing agreements and/or in the evaluation of new business development opportunities.
May assist in scientific/medical education of investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information.
May represent the medical function on cross-functional integrated teams for medical affairs 'activities. May represents AbbVie at external meetings including investigator meetings, scientific association meetings, etc.
May assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.
May assist with the scientific review, development, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials for assigned therapeutic area(s) within Medical Affairs. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.
May assist in the development of scientifically accurate marketing materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.
Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area.