Sr. Medical Director, Medical Affairs (Achondroplasia Lead)

7+ years

$265,000 - $345,000 USD

Remote, USA

10 Nov. 27, 2024

Job Description

Job Type: Remote Education: MD, PharmD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Sr. Medical Director, Medical Affairs (Achondroplasia Lead)
Location: Remote - United States
Salary: $265,000 - $345,000 USD
Company: QED Therapeutics & BridgeBio Pharma

About QED Therapeutics & BridgeBio Pharma

QED Therapeutics, a BridgeBio Pharma affiliate, is focused on developing targeted treatments for FGFR-driven skeletal dysplasias, particularly Achondroplasia. This genetic condition leads to short stature and potential medical complications. BridgeBio aims to bridge academic advancements in genetic science with the delivery of transformative medicines for genetic diseases and cancers.

Responsibilities:

Medical Content Development: Lead and organize advisory boards and symposia supporting pipeline programs.
Stakeholder Engagement: Collaborate with clinical consultants, KOLs, investigative sites, and the research community to support the Achondroplasia program.
Field Medical Strategy: Co-develop strategies with the Senior Field Medical/MSL team lead.
Clinical Support: Contribute to and collaborate with clinical development on ongoing clinical trials (phases 2-4).
Scientific Data Disclosure: Work with cross-functional teams to establish a strategy for scientific data disclosure to support registration and launch.
Publications and Presentations: Collaborate with Scientific Communications to prepare external publications and presentations.
Team Collaboration: Function as the medical representative on cross-functional teams and project meetings.

Required Qualifications:

MD, PharmD, or equivalent.
7+ years of experience in drug development, clinical investigation, or as a physician-scientist.
Experience in rare disease fields or pediatric endocrinology is a plus.
Expertise in clinical research, product development, and approval processes.
Experience in product launch development and execution.
Knowledge of regulatory affairs impacting Medical Affairs.
Strong interpersonal, leadership, and communication skills.

Preferred Qualifications:

Experience in strategy and execution within pharmaceutical product development.

What We Offer:

Competitive salary and market-competitive compensation (Base, Bonus, Equity, Health, Welfare, and Retirement Programs).
Flexible PTO and rapid career advancement opportunities.
Learning and development resources to enhance professional growth.
A collaborative, data-driven environment inspired by values like putting patients first and transparency.
Opportunity to work on multiple BridgeBio Pharma programs across diverse therapeutic areas.

BridgeBio promotes a decentralized model that empowers teams to make decisions closest to the science, fostering a culture of independence and entrepreneurial thinking.

To learn more about the company and our mission, visit QED Therapeutics and BridgeBio Pharma.

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Sr. Medical Director, Medical Affairs (Achondroplasia Lead)

Job Description

About QED Therapeutics & BridgeBio Pharma

Responsibilities:

Required Qualifications:

Preferred Qualifications:

What We Offer:

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