Medical Science Liaison - Cardiovascular

About The Job

One shared journey is moving us forward at BristolMyers Squibb. Around the world we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. And driven to make a difference from innovative research to handson community support.

Looking for opportunities to learn and grow professionally working alongside smart talented colleagues who are committed to helping patients prevail over serious diseases

Join us on this journey...and imagine just how far well go.

Role Summary

MSL embody our medical mission in becoming a trusted agile partner who engages in relevant dialogue and delivers timely high impact data and insights that advance the science or accelerate access optimise medical practice and drive appropriate adoption of BMS medicines. The MSL role is a fieldbased role. It is anticipated that a MSL will spend a minimum of 6070% of their time in the field with external customers.

The primary role of MSL is to develop and maintain contacts with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of interactions is to ensure patients have access to BMS medicines to ensure their safe and appropriate use through peer to peer discussions aligned with medical strategies and needs expressed by the stakeholders. The scientific dialogue focuses on scientific/clinical information around disease management and BMS products in a fair and balanced way and includes appropriate Health Economics and Outcomes Research (HEOR) data. This role is for innovator molecule in CV therapy area and person will work in prelaunch launch and immediate post launch phase.

Key Responsibilities

External Environment and Customer Focus

• Develop and maintain interactions with Thought Leaders appropriate HCPs and access stakeholders within a given geography to answer scientific unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1 1 group presentation; remote etc).
• Develop and execute a medical interaction plan with Key accounts (Army Railways CGHS etc.) as per the needs of the stakeholders and the overall medical strategy
• Effectively present information to HCPs and be able to respond to questions ensuring medical accuracy and compliance with local procedures ethical and legal guidelines and directives.
• Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update their own knowledge in treatment strategies products unmet medical needs clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers.
• Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development.
• Report safety information including adverse events in accordance with BMS Standard Operating Procedures.

Contribute to the Country Medical Plan

• Develop territory Field Medical plan and TL Interaction plans based on therapeutic area objectives and TLs needs.
• Execute certain medical plan activities as assigned.
• Adopt institution/account planning approach and contribute to crossfunctional institution/account plans.
• Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan.

Provide Medical Support

• As necessary and appropriate support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial Regulatory
• Pharmacovigilance Legal HEOR Market Access).
• Provide scientific support at promotional meetings by presenting unbiased scientific and clinical data by evaluating speakers and by giving support to BMScontracted speakers.

Support Clinical Trial Activities

• Support Interventional and Non Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products as agreed with local medical management and as defined by the study scope document.
• Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators as agreed with local medical management.
• Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document.
• Support HCPs in the ISR submission process as agreed with local medical management.
• Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies and alert appropriate BMS personnel to any identified Adverse Events.

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Remote Work :

No