Associate Project Manager, Early Phase

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🕒 April 24

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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

• Functions as a member of the Early Phase Project Management Team at Emerald Clinical. • Provides project management expertise for commercial and academic studies. • Operates cross functionally to ensure effective project outcomes. • Responsible for study management activities including team leadership, client communication, financial management, and overall study delivery. • Develops, conducts, and completes research projects under guidance of experienced Project Manager or Portfolio Delivery Leader. • Coordinates project activities in accordance with project specific documentation, applicable SOPs, ICH GCP, and regulatory requirements. • Maintains effective professional relationships with external customers, investigators, and vendors. • Helps identify project specific activities needing outsourcing and involved in selection of suitable vendors.

🎯 Requirements

• Bachelor’s or Masters degree in a science or related field • Previous experience working on clinical projects within an academic, CRO or pharmaceutical company environment • Relevant work experience recommended for this role may be approximately five (5) years of industry experience • Prior CRA experience preferred or site management role experience, trial coordination or relevant industry experience required • Previous experience supervising project related tasks of other people • Previous exposure to client-facing interactions and/or client management • Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions.

🏖️ 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.