About

• 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.
• About the Role
• As a Senior Medical Monitor, you will play a crucial role in ensuring the safety and integrity of clinical trials. You will provide medical and scientific expertise to clinical research projects, working closely with cross-functional teams to support study execution and compliance with regulatory requirements. This position is fully remote in Europe.
• Your Responsibilities
• • Provide medical oversight for clinical trials, ensuring patient safety and adherence to protocol.

• • Serve as the primary medical contact for study teams, investigators, and sponsors.

• • Review and assess adverse events, serious adverse events (SAEs), and safety reports.

• • Contribute to protocol development, study design, and medical monitoring plans.

• • Participate in investigator meetings, site initiation visits, and data monitoring activities.

• • Support regulatory submissions by providing expert medical input.

• • Collaborate with clinical operations, biostatistics, and regulatory teams to drive successful trial outcomes.
• About You
• • Medical Doctor (MD) qualification is required.

• • At least 5 years of experience as a Medical Monitor in clinical trials with vast experience in Renal Trials.

• • Strong knowledge of GCP, ICH guidelines, and regulatory requirements in North America.

• • Experience in safety monitoring, adverse event assessments, and medical data review.

• • Excellent communication and collaboration skills to work effectively with global teams.

• • Ability to provide strategic medical insights and problem-solving expertise.
• Why Join Us?
• 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.
• What We Offer

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.

• Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.
• We are an equal-opportunity employer and encourage applications from all qualified candidates.