Medical Science Liaison

ECLARO; New Jersey; Remote; USD 130,031 - 137,911; Full time

Benefits offered by this job

401k with Merrill Lynch

Commuter benefits

Medical, Dental & Vision Insurance

Job summary

A biopharmaceutical company is seeking a Medical Science Liaison to capture medical insights and engage with the clinical community in New Jersey. The role requires strong clinical knowledge in hematology and prior experience as an MSL. The ideal candidate will possess excellent communication skills and the ability to work independently while engaging with external stakeholders. This opportunity offers a competitive pay rate and comprehensive benefits.

Qualifications

• Minimum 3 years clinical or research experience in hematology or as an MSL in lymphoma or multiple myeloma.
• Cell therapy experience strongly preferred.
• Ability to work independently and in cross-functional teams.

Responsibilities

• Collaborates with thought leaders to gain insights on the clinical landscape.
• Engages with medical societies and develops connections with key thought leaders.
• Provides recommendations based on field knowledge for study feasibilities.

Skills

Clinical experience

Research experience

Communication skills

Team collaboration

Education

MD, DO, PharmD, DNP, or PhD

Job description

Job title

Medical Science Liaison (MSL) – Remote, NJ

Base pay range
$94.39/hr - $100.11/hr

Job Number: 25-05149

Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Medical Science Liaison for our client in remote New Jersey. ECLARO’s client is a leader in the biopharmaceutical industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Position overview

The MSL captures medical insights and acts as a clinical & scientific advisor to cross-functional partners. The MSL engages with the medical community to address questions beyond approved assets and indications, focusing on pre- and peri-launch activities or according to lifecycle needs of the brand. This role is field-based, with majority time spent in the field interacting with external stakeholders (investigators, clinical thought leaders) while supporting internal stakeholders and maintaining a high level of therapeutic expertise. Travel expectations will be based on territory assignment and team needs.

Responsibilities

• Medical Engagement
  • Collaborates and engages in scientific dialogue with TLs to gain insights on the clinical landscape and develop a medical plan focused on product/disease area and launch objectives.
  • Engages in scientific and clinical conversations to support launch activities and lifecycle management (LCM).
  • Engages with medical societies, patient advocacy groups (PAGs), and guideline committees as appropriate.
  • Provides training for external speakers as needed.
  • Strategically engages payers in pre- and peri-launch phases (with fHEOR and Account Executives).
  • Provides medical support to address unsolicited HCP questions in real time (face-to-face and via Medical on Call).
  • Develops credible connections with key thought leaders in the therapeutic area through high-quality peer-to-peer dialogue.
  • Documents activities and achieves annual goals; leverages digital capabilities to enhance medical engagement.
• Clinical Trial Engagement
  • Provides recommendations and insights on study feasibilities within the therapeutic area based on field knowledge and investigator contacts, as agreed with home office medical and Global Development Operations (GDO).
  • Liaises with key accounts to understand clinical barriers to patient access and ensure equity in trial access.
  • Leads major evidence read-outs with trial investigators (e.g., Phase 3 top-line data).
  • Supports interventional and non-interventional research (NIR) studies to facilitate recruitment and discuss safe and effective use of products, as defined by the study scope.
  • Ensures pharmacovigilance procedures are understood and followed by investigators; alerts appropriate personnel to identified Adverse Events.
  • Supports CRO-sponsored studies as applicable, per study scope.

Qualifications

• MD, DO, PharmD, DNP, or PhD required.
• Minimum 3 years clinical or research experience in hematology OR 3 years as an MSL in lymphoma or multiple myeloma landscapes.
• Cell therapy experience strongly preferred.
• Ability to work independently and in cross-functional teams.
• Working knowledge of US legal, regulatory, and compliance guidelines relevant to interactions with health-care professionals.
• Ability to partner and maintain relationships within the medical community.
• Excellent communication, presentation, and time management skills.
• Ability to translate scientific or clinical data into understandable information to help physicians serve patients.
• Scientific Agility
  • Engage in balanced dialogue about data; explain data in a way that resonates with TLs/HCPs.
  • Strong knowledge of clinical practice and evolving healthcare delivery models.
  • Ability to critically appraise scientific publications and understand trial design and methodology (GCP, regulatory requirements).
  • Understand treatment paradigms and competitive landscape; frame information in a compliant, persuasive way.
  • Maintain strong learning mindset and stay current with latest data.
• Patient Centricity
  • Understand the patient journey and maintain a patient-focused mindset.
• Customer-Focused / Enterprise Mindset
  • Understand enterprise objectives and priorities; demonstrate a winning mindset, resilience, and adaptability.
  • Embrace new ways of working and technology; drive organizational performance and cultivate HCP relationships.

Pay rate and benefits

Pay Rate: $94.39 - $100.11 / hour

Benefits: 401k with Merrill Lynch, commuter benefits, and eligibility to purchase Medical, Dental & Vision Insurance through ECLARO

How to apply

If interested, you may contact:

Sofia Dela Torre
[e-mail]
[phone]
LinkedIn | Sofia Dela Torre

Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, national origin, age, genetic information, disability, protected veteran status, or any other legally protected status, in compliance with all applicable laws.