Medical Science Liaison Venezia

Medical Science Liaison
Venezia
Veneto, Venezia

Do you have the passion and commitment to join a group whose mission is to develop treatments that clearly and profoundly impact patients suffering from rare diseases?

Does it excite you to be a part of a patient-focused company developing potential new therapies that could dramatically improve patients' lives with limited to no current treatment options?

If so, we encourage you to share your aspirations and career goals. The pharmaceutical company is focused on restoring healthy immune system function by developing novel therapeutics to treat chronic neutropenic disorders, a rare primary immunodeficiency.

We are advancing a novel late-stage clinical candidate that has the potential to become a new standard of care for patients with these disorders.

We know that developing innovative, new medicines is challenging, and we invite new colleagues who share our values and commitment to join us in achieving our mission. Align your values with determination and passion for groundbreaking science. You can use your extensive medical science, education, and research knowledge to boost our innovative scientific efforts and help our patients. We provide a collaborative environment with a team-based approach, where our mission steers our values, behaviours, and creativity. Accountabilities and Responsibilities:The Senior Medical Science Liaison (MSL) is a field-based clinical and scientific expert primarily responsible for disseminating clinical and scientific information to support the Client's Rare Primary Immunodeficiencies (PID) and Chronic Neutropenia portfolio.

They will be mainly responsible for communicating clinical and scientific information related to applying the Client's molecules across all therapeutic areas to Healthcare Practitioners (HCPs), payers, and professional societies.

Other critical aspects of this role include gathering and communicating insights from key external stakeholders to inform and guide strategic planning, supporting ongoing data generation activities and collaborating with internal Client stakeholders. Build and execute a territory strategy and tactical plan in alignment with the medical affairs plan. Develop and maintain effective professional relationships with key external stakeholders to build a network of Key Opinion Leaders for medical and scientific exchange and research initiatives. Provide in-depth drug and disease state medical and scientific information to HCPs. Have clinical and scientific discussions with potential investigators to ensure the overall quality of study endpoints, including, but not limited to, understanding of clinical protocols, study feasibility, and enrollment.

Convey KOL and site staff feedback and insight to internal and external teams. Conduct targeted conversations with the investigators and site staff regarding operational challenges, including but not limited to patient recruitment and retention. Communicate field feedback and actionable insights to internal Client stakeholders regularly. Attend key medical congresses at the national level and regional society meetings supporting scientific and corporate goals. Keep updated with product information, scientific evidence, and therapeutic landscape. Hold knowledge of industry trends, relevant healthcare systems, and the regulatory and payor environment. Serve as a liaison to HCPs, professional organisations, and disease state advocacy groups.

Support the efforts of patient support groups and educational foundations. Provide medical and scientific input into the planning and executing advisory boards and MSL roundtables.

Work with KOLs to review presentations and provide additional medical education where requested. Work with the client field personnel to provide in-depth disease state and product medical education. Generate Custom Medical Response Letters upon receipt of medical inquiries and respond to unsolicited Medical Information requests. Respond to unsolicited requests regarding interest in investigator-sponsored studies (ISS) and support their submission through an appropriate internal process. Partner closely with investigators and internal stakeholders to support site identification and clinical trial enrollment. Accountable for meeting corporate goals and objectives while complying with applicable policies and regulations. Requires 60 – 70% travel. Requirements: Proven Experience, Skills, and Education:PharmD, PhD, or MD preferred, but NP/PA/MSN with clinical experience will be considered. Minimum five years of MSL experience. Rare Disease and Immunology and/or Hematology experience is preferred but not required. Creative problem-solver with strong business acumen and skills. Able to work independently with exceptional time management and organisational skills. Proven track record of success in establishing relationships with opinion leaders. Ability to understand and communicate evidence-based scientific information. Ability to work collaboratively and cross-functionally, showing sound decision-making and accountability. Experience in clinical research, patient recruitment, and investigator-sponsored trials. Passionate about making a meaningful difference in patient care. This role is field-based, and residency in the assigned territory is required.

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