Senior Project Manager, Scientific Leadership and Medical Affairs

At Emerald Clinical Trials
, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post‑marketing.

Our therapeutic expertise spans renal
, cardiometabolic
, and oncology
, areas where we make a significant impact on improving global health.

At the heart of our success is our ability to combine global reach with local knowledge. Our on‑the‑ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results – bringing therapies to patients in need.

We are seeking a Project Manager, Scientific Leadership, home‑based in the EU, to support the delivery and coordination of our Scientific Leadership services across global studies. This unique role sits at the intersection of science, operations, and strategic project delivery. You will work closely with Key Opinion Leaders (KOLs), Scientific Leads, and internal teams to implement scientific advisory activities that shape study design and execution.

You’ll also coordinate the operational aspects of steering committees, endpoint adjudication, and other scientific governance bodies throughout the clinical trial lifecycle.

• Lead and manage operational delivery of scientific leadership components within assigned projects
• Serve as key liaison for Regional and National Scientific Leads
• Coordinate communications, meetings, contracting, and payments related to scientific committees and advisors
• Maintain real‑time project trackers, metrics, and reporting documents
• Collaborate cross‑functionally to ensure scientific governance is integrated smoothly into project execution
• Contribute to client deliverables, including progress reports and strategy presentations
• Support continuous improvement of scientific leadership processes and templates
• Ensure compliance with SOPs, ICH‑GCP, and regulatory requirements
• Provide backup support to the Project Lead as needed
• Support knowledge sharing and team development within the organisation

• Bachelor’s degree in a life sciences, health, or related discipline
• Experience liaising with scientific or medical professionals, including KOLs or investigators
• Strong understanding of clinical research processes, scientific governance, and stakeholder engagement
• Familiarity with ICH‑GCP and clinical trial regulations
• Excellent communication, organisational, and project management skills
• Able to manage multiple priorities in a fast‑paced environment
• Fluent in written and spoken English
• Tech‑savvy with proficiency in Microsoft Office and virtual collaboration tools
• Extensive experience in clinical research, preferably within a CRO or academic setting

At our core,
Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

Here’s what makes us stand out:

• Purpose‑Driven Work
  :
  You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
• Global Reach, Local Expertise
  :
  Our teams connect with local communities, building trust and meaningful engagement for every trial.
• Collaboration and Innovation
  :
  Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.

We understand that great work happens when people feel valued and supported. That’s why we provide:

• 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.

We are an equal‑opportunity employer and encourage applications from all qualified candidates.