Regional, Medical Adviser, South
|Job Title:||Regional, Medical Adviser, South|
|Salary:||strong benefits package and incentives|
|Start Date:||Q2 2019|
|Contact Name:||Vladyslav Babych|
|Job Published:||February 25, 2019 18:28|
Regional Medical Advisor positions non-promotional hybrid role that combines traditional field-based medical activities and strategic responsibilities within designated region. The major objective of the role is to provide a scientific support to the assigned therapeutic area to ensure implementation of the scientific strategy leading to optimal patient treatment and future business success.
The Regional Medical Advisor provides unbiased scientific information and medical education, drives data generation, establishes value-adding partnerships with healthcare professionals engaged in Iron deficiency Anaemia care and supports the commercial teams.
The Regional Medical Advisor works to shape the Iron Deficiency Anaemia care through company products, research and customer services excellence.
*Provide high quality scientific information to healthcare professionals (HCPs) in response to specific requests.
*Support implementation of local best-practice protocols for the treatment of iron deficiency anaemia (IDA).
*Support data generation through HCP-initiated projects by advising on medical writing, data analysis, and publication, where required.
*Initiate and maintain strong relationships with Key Opinion Leaders (KOLs).
*Develop and roll-out educational concepts in target therapeutic areas focusing on IDA awareness and screening, guideline recommendation and IDA treatment.
*Support the provision of educational meetings focused on IDA management by interaction with HCP speakers to provide briefings around compliance, product information, clinical and scientific data, and support development of presentations.
*Proactively identify areas of development for assigned therapeutic area, input into medical plans and execute medical affairs strategy by taking actions that lead to advances ensuring optimal patient treatment.
*Take an active role in clinical trials: Input into the clinical development plan, study design and protocols to ensure that UK needs are addressed. Proactively identify data gaps and work with relevant stakeholders to fill unmet needs. Drive company-sponsored studies and have full responsibility for assigned investigator-sponsored studies ISS).
*Provide scientific support to sales and marketing teams: provide internal scientific training, input into the development of company materials and act as a compliance reviewer for sales/ marketing materials, where necessary.
*Act to the highest ethical standards, develop an excellent understanding of the ABPI Code Practice and serve as a compliance adviser for internal teams, where necessary.
*Fulfil company responsibilities as defined in the PVG SOPs related to medical enquiries and drug safety information, and proactively collect information on the safety profile of company products.
The proportion of time dedicated to each activity varies depending on the seniority of the individual and the business need.
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