Executive Medical Director, Alzheimer’s Disease

🕒 March 25

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NewAmsterdam Pharma Corporation

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2019

🧬 Biotechnology

💊 Pharmaceuticals

💰 $175.3M Post IPO equity on 2024-03

Biotechnology • Pharmaceuticals

NewAmsterdam Pharma Corporation is a clinical-stage biopharmaceutical company focused on developing therapies for cardiovascular disease and other lipid-related conditions. The company is advancing obicetrapib, a CETP inhibitor, and other programs aimed at lowering LDL-C and reducing cardiovascular risk for patients who have unmet needs despite existing lipid-lowering treatments. NewAmsterdam emphasizes science-backed development, clinical trials, and patient-focused initiatives.

📋 Description

• Lead the formulation and implementation of the Clinical Development Plan • Protocol design: lead the clinical trial design to ensure it supports the strategic objectives • Work with CRO medical monitors and sites to review and respond to site queries related to protocols • Support the PV department in oversight of the medical & safety monitoring conducted by the CRO • Ensure successful completion of trial-related documents with cross-functional team members • Support site and subject retention • Analyze, evaluate, interpret, and report clinical data • Contribute to drafting and reviewing of clinical documents, manuscripts, presentations, and regulatory submissions • Provide clinical science related leadership to study teams • Contribute to ad-board meetings, executive committee meetings • Responsible for high quality collaboration with external stakeholders • Contribute to regulatory strategy and development of sections of the IB • Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance • Collaborate with cross-functional colleagues to optimize product development • Assist in portfolio management and commercial activities as needed • Adhere to rigorous ethical standards • Travel as required both domestically and internationally for scientific meetings

🎯 Requirements

• M.D. degree: Completion of ACGME-accredited residency and fellowship strongly preferred • Board-certified required, with specialty in Neurology • Physician licensure in at least one state strongly preferred if based in US • At least 8-10 years of industry experience (minimum of 5 years in clinical trial design and execution) • Thorough knowledge of clinical trials design, processes and GCP and ICH guidelines • Working knowledge of US FDA and EMEA AD related regulations and guidelines • Ability to perform literature research, analyze and author clinical trial publications • Robust analytical skills to analyze and interpret clinical trial data, evaluate study outcomes, and generate scientific evidence supporting product development • Comfortable in communicating and interacting with investigators, KOLs, and advisors • Multi-task while remaining organized and attentive to detail • High work ethic, a trustworthy and collaborative team player • Demonstrate sound judgement in terms of handling complex, confidential, and regulated information • Ability to travel approximately 20-25%

🏖️ Benefits

• Health insurance • Dental and vision coverage • Term life and disability coverage • Retirement plans