Medical Director – Ophthalmology

November 22

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Logo of Parexel

Parexel

Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

📋 Description

• Initiate and maintain medical and consultative relationships with clients • Consult on early engagement and pre-award efforts • Serve as a medical monitor for contracted projects • Deliver all medical support required for successful delivery of the projects according to contracted agreement with the sponsor • Provide medical expertise / leadership in Proposal Development Teams (PDTs) for client bid pursuit meetings • Client Relationship Building & Engagement, including soliciting and addressing client feedback • Participate in initiatives, mentoring junior MDs and/or managing a team of physicians • Focus on Medical Monitoring Delivery & PV Support

🎯 Requirements

• Experience in clinical medicine (general or specialist qualifications) with Fellowship or specialty training in Ophthalmology • A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design/execution, preferred • Clinical practice experience • Good knowledge of the drug development process including drug safety, preferred • Experience in Pharmaceutical Medicine, preferred • Experience leading, mentoring and managing individuals/ a team, preferred • US Board certified in Ophthalmology or Canadian equivalent • Experience as a Physician in Industry or as a clinical trial investigator is required • Previous CRO experience is strongly preferred • Medically qualified in an acknowledged medical school with completion of at least basic training in clinical medicine (residency, internship) • The ability to travel 15% domestically or internationally is required

🏖️ Benefits

• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development

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