Area Field Medical Manager
1 week ago
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.
BioMarin’s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases. Come join our team and make a meaningful impact on patients’ lives.
**Field Medical Manager (FMM)** is the external-facing scientific expert**
FMM is the external-facing scientific expert on the company product(s) and therapeutic area(s), with the core responsibility of scientific engagement. This consists of the establishment and maintenance of ethical and highly scientific peer to peer relationships with leading Health Care Professionals (HCPs) at major academic institutions and hospitals. Based on high-quality response to medical inquiries and generation, interpretation and communication of scientific data with leading HCPs, FMMs could potentially improve - through meaningful scientific exchange - the clinical management of patients and their quality of life.
**FMM Core Responsibilities**
- Scientific engagement
- Evidence generation support
- Insight management
- Internal partnerships
**FMM Key Activities**
- ** **Scientific engagement**
- Scientific engagement with Key Opinion Leaders (KOLs) in healthcare, academia, payers (as required), and government organizations (as required), to provide appropriate scientific information about company products and related therapy area, gather insights and expert opinions from relevant HCPs. Thus, becoming a trusted scientific partner by enhancing the understanding of the scientific and medical value of BioMarin products _(pre-, peri
- and post-launch) _
- Proactive KOL / treatment center mapping and planning according to the scientific strategic needs of the product or therapeutic area _(pre-, peri
- and post-launch)_
- Development and implementation of Scientific Exchange meetings at hospital, national or regional level. Support the Area Director / Therapy Area (TA) Lead on the development and implementation of regional or national Scientific Educational Programs in line with BioMarin’s scientific needs, including the scientific briefing of the speakers _(pre-, peri
- and post-launch) _
- Conduct drug administration (infusion) readiness trainings upon request _(pre-, peri
- and post-launch) _
- Support post-marketing studies as required _(peri-/post-launch), _in collaboration with study management by
- Checking and supporting study site readiness
- Performing on site product risk management and education/information
- Clarify process and procedures for independent research programmes upon request.
- Scientific conference support _(pre-, peri
- and post-launch)_
- Pre-conference
- Collaborate with colleagues to identify attending HCPs and arrange meetings with them
- Meet regional/global colleagues as necessary (pre-conference meetings)
- During the conference
- Attend relevant scientific sessions.
- Engage in scientific exchange (ad-hoc, as follow-up of previous interaction)
- Staff BioMarin medical booths in their area of expertise
- Post-conference
- Develop and deliver a meeting report to be shared cross-functionally
- Prepare post-conference updates in line with country legislation
- Responds to costumer requests with relevant scientific information and coordinate with Medical Information the provision of answers for on
- or off-label queries _(pre-, peri
- and post-launch)_
- Reactive provision of information to local Patient Advocacy Groups (PAGs) in lieu of Area Medical Director, TA Lead and in line with Business Code of Conduct in collaboration with Patient Advocacy _(pre-, peri
- and post-launch)_
- **
**Evidence generation support**
- Work with investigators in company sponsored studies supporting (by request) Clinical Operations and/or Study Management resources by sharing insights on potential study sites in alignment with the Area Medical Director / TA Lead, based on their scientific capabilities, administrative readiness, and stakeholder interests, partnering with clinical operations and Contract Research Organizations (CROs) to ensure surveillance and compliance with study programs, and proactively engaging with investigators both during startup and throughout the study period to maintain interest in and education about the study
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