Medical Director

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Emerald Clinical

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2000

🧬 Biotechnology

💊 Pharmaceuticals

Biotechnology • Pharmaceuticals

Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.

📋 Description

• Lead medical design and oversight for major projects; review and approve protocols, IB, ICF, SAP and key medical documents; provide medical input on feasibility, risk mitigation and endpoint selection. • Oversee drug safety and AE/SAE management; review medical adjudication and causality assessments; collaborate with PV teams and external experts. • Provide medical guidance to project teams, biostatistics and data management; participate in key milestones (per request or specific plan). • Support regulatory interactions and ethics committees; draft/review medical position papers, CSRs and regulatory responses. • Lead and mentor Medical Monitors/Managers; develop capability plans and participate in performance and resource decisions. • Establish/improve medical governance, QA processes and SOPs to ensure high-quality clinical and medical deliverables. • Serve as company medical representative in client meetings, support RFPs (bidding) and engage in medical communications with IRBs/ethics committees and regulators. • In some case role of Safety Physician may be taken.

🎯 Requirements

• Medicine, Pharmacy, or life sciences education background, master’s degree or above is preferred • 10 years’ or above working experience and 5+ years of medical monitoring or medical manager or Sponsor preferred • Strong leadership, cross-functional collaboration and project management skills; decisive in a fast-paced environment. • Fluent verbal and written English, able to communicate with international clients and regulators • Ability to work independently and handle multiple tasks simultaneously under pressure. • Successful interactions with key opinion leaders and investigators • Strong knowledge of GCP, ICH, NMPA/FDA/EMA regulations and review processes; experience in pharmacovigilance and regulatory communication. • Global, cross-cultural perspectives and customer orientated.

🏖️ Benefits

• Competitive Compensation : A tailored salary and benefits package to reflect your skills and experience. • Flexibility : Enjoy hybrid or remote working arrangements, depending on your location and role. • Career Growth : Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role. • Employee Wellbeing : Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events. • Global Opportunities : Be part of a company with international reach, offering you exposure to diverse projects and clients.