Clinical Development Medical Director – Cardiometabolic

🕒 July 23

🇺🇸 United States – Remote

💵 $274.8k - $371.8k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 45%

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Amgen

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1980

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 $28.5G Post-IPO Debt on 2022-12

Healthcare • Biotechnology • Pharmaceuticals

Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.

📋 Description

• Lead the early phase clinical development of compounds from first-in-human studies through proof-of-concept • Collaborate on teams to support the design and delivery of early phase clinical trials • Support protocol development, study start-up, data review, monitoring and analysis activities • Contribute to the design and implementation of early clinical development strategies for cardiometabolic/general medicine therapeutic candidates • Contribute to clinical development plans, clinical study protocols, informed consents, Investigator Brochures, and Ethics Committee and regulatory agency submissions • Review and evaluate clinical study safety, efficacy, pharmacodynamic and pharmacokinetic data • Contribute to the strategy and use of clinical biomarkers • Collaborate with Precision Medicine, Research, Late Development, Regulatory, Safety and Commercial colleagues • Evaluate external licensing or partnering opportunities • Collaborate with external experts to provide biomedical expertise and strategic guidance to Early Development teams

🎯 Requirements

• MD or DO degree from an accredited medical school • 2 years of industry or academic/basic sciences/clinical research experience • Board certification or eligible • Residency training in Cardiology, Internal Medicine or relevant subspecialty • Understanding of cardiometabolic and general medicine pathophysiology • Experience in basic research and/or clinical trial methodology • 4+ years of relevant drug development experience in the pharmaceutical industry and/or academia, preferably in early stage clinical trials • Experience collaborating with pharmaceutical sponsors • Experience designing, monitoring and implementing clinical trials and interpreting trial results • Demonstrated leadership qualities; capable of conducting studies as part of a team • Experience within a matrix environment and contributing to decision-making and reaching alignment • Publication track record • Excellent interpersonal and presentation skills • Ability to communicate effectively with internal stakeholders, external partners and collaborators

🏖️ Benefits

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • A discretionary annual bonus program • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible • Career development opportunities • Work/life balance support