Medical Science Liaison, Radioligand therapies, South (maternity cover)

Salary Range:

Job Description Summary

Job Description

Medical Engagement 

• Execute Medical Expert (ME) engagement plans (MEEPs) aligned with TA strategic priorities. 

• Conduct unbiased, evidence‑based, peer‑to‑peer scientific exchange with HCPs and MEs, providing up‑to‑date medical and disease area information. 

• Ensure appropriate identification and mapping of MEs/Key Accounts, and proactively involve them when specific medical needs, scientific questions, or evidence gaps are identified. 

• Share, discuss, and contextualize new clinical data and publications. 

• Support ME/HCP education activities (e.g., hospital staff meetings, regional scientific events). 

• Ensure compliant, high‑quality scientific dialogue aligned with company guidance. 

Evidence Generation & Clinical Research Support 

• Systematically collect, synthesize, and communicate actionable external insights from clinical practice, scientific discussions, and competitive activities. 

• Inform local and regional medical strategy through real‑world feedback and emerging unmet needs. 

• Support identification and qualification of potential study sites. 

• Facilitate communication between sites and internal teams to optimize study execution. 

Medical Education & Scientific Communication 

• Contribute to planning, execution, and follow‑up of local/regional medical education activities. 

• Provide scientific support for events, symposia, and internal or external educational initiatives. 

• Contribute scientific insights to shape country medical plans and disease area strategies. 

• Maintain a strong understanding of the therapeutic landscape, emerging data, and competitor environment. 

Medical Partnerships 

• Build and maintain strong partnerships with Medical Experts, scientific societies, and academic institutions to support collaboration and scientific leadership in the TA. 

• Act as a scientific resource for internal partners, providing clinical context, data interpretation, and training. 

• Represent the company as the credible scientific ambassador in the TA, contributing to a positive reputation with key stakeholders and institutions. 

• Strengthen the medical ecosystem by shaping joint value creation initiatives, evidence-based collaborations, and multistakeholder partnerships. 

Compliance & Governance 

• Ensure all engagements, materials, and activities meet ERC, regulatory, and medical governance requirements. 

• Maintain accurate reporting, CRM documentation, and activity tracking. 

Key Performance Indicators 

• Input Indicators (what the MSL prepares or brings into their work) 

• In-field days, i.e., days per month with one or more face-to-face or virtual scientific interaction ≥ 15 

• Process Indicators (how the MSL performs their work): 

• HCP Coverage with scientific interactions per calendar quarter ≥ 80% 

• Face-to-Face scientific interactions ≥ 80% 

• Productivity, i.e., face-to-face or virtual scientific interactions with HCPs per in-field day ≥ 2.0 interactions/day. 

• Output Indicators (what the MSL directly delivers) 

• HCPs with assessed scientific engagement ≥ 80% 

• Outcome Indicators (effects achieved through the MSL’s outputs) 

• Positive evolution of assessed scientific engagement scores, with documented progression toward higher advocacy. 

• Impact Indicators (contribution to Novartis, the healthcare system, and patients) 

• Evidence of enhanced strategic value to the organization through insight-driven engagement and consistent scientific excellence. 

Ideal Background 

Education: 

• Advanced scientific degree (MD, PharmD, PhD, MSc in Life Sciences) or equivalent. 

Languages: 

• Portuguese 

• English 

Experience/Professional Requirement: 

Experiences: 

• Experience in Medical Affairs or clinical/scientific roles (field‑based experience preferred). 

• Demonstrated ability to engage in high‑quality scientific dialogue with HCPs/MEs. 

• Experience interpreting clinical data and scientific evidence. 

• Understanding pharmaceutical industry regulations, compliance, and scientific engagement standards. 

• Experience supporting clinical research is a plus. 

Functional Capabilities: 

• Strong scientific and clinical data interpretation skills. 

• Ability to collect, synthesize, and communicate insights. 

• High proficiency in scientific engagement and communication. 

• Understanding of evidence generation approaches (RWE, clinical trials, observational studies). 

• Ability to partner effectively in a matrix environment. 

• Strong planning, prioritization, and territory management abilities. 

Interpersonal Capabilities & Mindset: 

• Scientific curiosity and growth mindset. 

• Ability to influence without authority  

• Acts with credibility and clarity of purpose to build and maintain effective and collaborative relationships 

• Collaborative, cross‑functional orientation. 

• Clear, impactful communication; ability to simplify complex science. 

• Adaptable, resilient, and comfortable navigating ambiguity. 

• High integrity, ethical judgment, and a patient-centric mindset guiding all interactions. 

• Rigorous process stewardship, following internal procedures precisely, maintaining high documentation standards and proactively addressing gaps. 

Skills Desired