Eclaro
Job title
Medical Science Liaison
(MSL) – Remote, NJ Base pay range
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV. $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 Sofia.DelaTorre@eclaro.com (332) 206-0779 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.
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Medical Science Liaison
(MSL) – Remote, NJ Base pay range
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV. $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 Sofia.DelaTorre@eclaro.com (332) 206-0779 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.
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