Who We Are

Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.

With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.

Global Expertise. Local Insight. Real Impact.

Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.

Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

Provides medical oversight and support for clinical trials, ensuring studies are conducted safely, compliantly and scientifically per GCP and the protocol. Act as senior medical contact for clinical development, protocol input, medical review, safety assessment and client/regulatory interactions

Your Responsibilities

• Review and provide medical input for study protocol, informed consent form (ICF), Investigator’s Brochure (IB), statistical analysis plan (SAP), and other study documents.

• Participate in study start-up, monitoring and closeout activities (if needed); provide medical training and support to monitors and project teams，include but not limited to investigator meeting, data monitoring committee and safety monitoring(review) committee etc.

• Conduct medical review of clinical data (listing or profile data), identify data quality or safety issues and propose remedial actions.

• Assess and manage adverse events (AEs/SAEs), perform medical adjudication, causality assessment and follow-up recommendations; prepare/review medical reports.

• Communicate with site investigator，sponsors, safety monitoring(review) committee, pharmacovigilance teams and regulatory authorities on medical matters, providing timely medical advice and documentation.

• Serve as company medical representative in client meetings, support RFPs（bidding） and engage in medical communications with IRBs/ethics committees and regulators.

• Complete other activities or tasks assigned by Medical Director.

In some case role of Safety Physician may be taken.

Responsibilities ：

• Conduct medical safety relevant tasks according to regulation and internal procedural documents, including product safety monitoring, review and preparation of safety report, Risk Management Plan, DSUR, PSUR etc.

• Keep close collaboration with Medical Director/Manager (if safety physician and medical monitor are not the same person in one project), DS personnel provide in-depth evaluation and solution for safety issues.

About You

• Medicine、Pharmacy、or life sciences education background, Master’s degree or above is preferred

• 7-10 years’ or above working experience and 5+ years of medical monitoring or medical manager or Sponsor preferred）

• Oncology or Immunity project experience in mandatory

• Fluent verbal and written English, able to communicate with international clients and regulators

• Ability to work independently and handle multiple tasks simultaneously under pressure

• Excellent communication skills and cross-functional coordination and problem-solving skills.

• Global, cross-cultural perspectives and customer orientated

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