Job Title: Medical Science Liaison Manager
Role Details
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The Role
- Develop and/or implement unbiased and non‐promotional scientific exchange meetings and educational activities:
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- Provide scientific/educational presentations to HCP regarding:
- Accord Healthcare products (on‐label & off‐label indications), or on Accord Healthcare compounds in development,
- Accord Healthcare products (on‐label single‐product presentation) but mainly on disease area management,
- Organize or support legitimate scientific exchange meetings,
- Contribute to/implement non-promotional medical education programs in the field,
- Contribute to the scientific publication program, if required,
- Organize non-promotional satellite symposia in regional (in‐country) congresses.
- Provide scientific/educational presentations to HCP regarding:
- Generate and share insight from HCP to nurture Accord Healthcare’s strategy:
- Collect, analyse, and report actionable scientific insight from HCP related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment,
- If appropriate, organise or support Advisory Boards at Regional level (in‐country),
- Attend and report insights from major National and Regional medical congresses,
- Engage and collaborate on specific initiatives with patient organisations in accordance with external/internal global and local guidance’s on Interactions with Patient Organisations and individual patients,
- Contribute to the dissemination of the information within the Company where appropriate,
- Report spontaneous adverse events and product‐related quality complaints in accordance to global and local Accord Healthcare SOP and the local law.
- Support for clinical development & Investigator Initiated Trials (data generation):
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- Coordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs’ objectives,
- Support the Accord Healthcare/ICTAS Sponsored Studies (Phase I to IV) operations (see attached Annex), when appropriate,
- Identify and drive opportunities to generate real‐world‐evidence data.
- Ensure internal cross‐functional collaborations as a scientific partner:
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- Develop Local Medical Plans,
- Develop publication and scientific project plan
- Set-up and schedule medical ad board
- Develop local standard responses, if required (in coordination with Medical Information Department).
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- Collaborate with commercial staff (Marketing, Sales or NPL team) to:
- Provide scientific expertise and training to commercial staff as required,
- Review and approve promotional materials in accordance with the local SOP and local law,
- Contribute to the review and approval of non‐promotional materials in accordance with the local SOP,
- Attend the local brand teams to bring additional scientific perspective,
- Attend and contribute to regional account planning/training sessions,
- Ensure speakers briefing for promotional meetings.
- Collaborate with commercial staff (Marketing, Sales or NPL team) to:
The Person
- Biomedical, Scientific University education ideally to post-graduate degree level e.g. MSc, PhD, MD, PharmD,
- Medical/Paramedical Practice or Research career (hospital and/or hospital related, university research, pharmaceutical industry research or medical affairs),
- Preferably at least 5 years of experience in pharmaceutical industry,
- Ideally proven experience and successful track record as an MSL or medical department professional in a previous company,
- Ideally, experience in one or more respective therapeutic areas associated with Accord Healthcare portfolio.
Other:
- Convey scientific information briefly, clearly, and precisely,
- Possesses a scientific qualification with significant scientific and/ or medical/clinical experience,
- The ability to understand, process, communicate and present scientific information to a high standard
- Possess excellent presentation skills,
- External customer focus with strong networking capabilities and integration with Tough Leaders,
- Excellent influencing, networking, presentation and communication skills and a proven track record of team cross-functional team working,
- Ability to manage multiple projects and adapt priorities according to business and strategic needs,
- Comply with highest ethical standards, with a working knowledge of relevant clinical regulations and industry standards as e.g., GCP,
- High level of emotional intelligence and motivation,
- Outgoing optimistic personality
The Rewards
How to Apply
A Bit About Us
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All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.
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