Medical Director – Heart Failure

🕒 September 24

🏛️ District of Columbia, Florida, +4 more states – Remote

🏛️ District of Columbia – Remote 🐊 Florida – Remote 🗽 New York – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote 🍑 Georgia – Remote

💵 $250k - $280k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 20%

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• Open for 49 days.
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Pharmacosmos Therapeutics Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2019

💊 Pharmaceuticals

🏥 Healthcare

Pharmaceuticals • Healthcare

Pharmacosmos Therapeutics Inc. is a therapeutics-focused company. The only information provided in the prompt is website cookie/stylesheet code, which contains no corporate, product, or pipeline details. Based on the company name and common usage, Pharmacosmos Therapeutics appears to operate in the pharmaceutical/therapeutics space within healthcare and likely focuses on development and/or commercialization of medical treatments. More specific details (therapeutic areas, products, or affiliations) are not available in the supplied content; I can look up public sources if you want a more detailed profile.

📋 Description

• Support successful execution and patient recruitment of the ICONIC-HF trial in the United States • Establish and maintain scientific relationships with investigators, study coordinators, and site personnel • Conduct regular virtual and relevant in-person site engagements • Understand local opportunities, challenges, operational barriers, and study execution issues within compliance, GCP, and trial governance frameworks • Serve as a US-based scientific liaison between participating sites and the HQ R&D ICONIC-HF trial team, US affiliate, and contracted CRO • Identify barriers affecting screening, enrollment, site engagement, or study execution; analyze root causes and help define mitigation activities • Facilitate cross-functional problem solving and escalation pathways • Support protocol understanding and scientific discussions within approved governance frameworks • Gather and communicate investigator insights, competitive intelligence, protocol feedback, and study observations • Organize regional sponsor-investigator touchpoint meetings • Identify and share compliant best practices from successful sites • Support site activation and engagement initiatives • Develop understanding of the US heart failure landscape, treatment pathways, referral patterns, unmet needs, evidence gaps, adoption barriers, and emerging trends • Map, prioritize, and engage regional and national heart failure thought leaders • Build scientific relationships with key experts beyond the ICONIC-HF investigator network • Generate insights supporting evidence generation, publication planning, congress activities, scientific communication, advisory boards, and launch readiness • Translate field insights into strategic recommendations with HQ and the US affiliate • Support investigator-sponsored research opportunity prioritization • Contribute to medical affairs strategy and IV iron launch-readiness planning • Partner with Medical Affairs, Strategy and Operations, Market Access, and Commercial colleagues • Maintain compliance with applicable governance requirements, laws, regulations, and corporate policies • Does not function as a CRA, perform monitoring or source data verification, own enrollment metrics or site performance targets, or manage day-to-day clinical trial operations

🎯 Requirements

• Experience within cardiology is required • Experience from clinical development, research and/or Medical Affairs • Demonstrated understanding of clinical trial conduct and investigator engagement • Experience collaborating with investigators, academic institutions, and cross-functional internal stakeholders • Ability to work effectively within cross-functional and matrix organizations • Strong scientific communication, relationship-building, and stakeholder-management skills • Ability to translate external insights into actionable recommendations for internal stakeholders • Advanced scientific or healthcare degree preferred, e.g., MD, PharmD, PhD, NP, PA, MSc, or equivalent • Basic GCP training or certification preferred; training can be provided for an otherwise qualified candidate • Heart failure expertise preferred • Cardiovascular outcomes trial experience preferred • Launch or pre-launch experience preferred • Experience engaging US-based KOLs and national thought leaders preferred • Experience working across both clinical development and medical affairs environments preferred • Established KOL network within heart failure/cardiology preferred • Requires budgetary responsibilities and discretion with confidential data • Approximately 65% travel • Must comply with applicable pharmaceutical laws, regulations, guidelines, corporate policies, FDA, EMA, and other global health authority regulations

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