Job Description

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

We are seeking an experienced Medical Monitor with deep expertise in Cardiovascular clinical trials to support our growing portfolio of studies across the US. In this key role, you will provide expert medical oversight and safety monitoring throughout the lifecycle of cardiovascular trials, ensuring the highest level of patient safety and protocol adherence.

Your Responsibilities

• Serve as the primary medical point of contact for assigned cardiovascular trials

• Provide medical and scientific input during protocol development, study design, and feasibility assessments

• Conduct ongoing medical data review, assess safety signals, and provide clinical input on adverse event reports

• Participate in investigator meetings and provide guidance to clinical teams on protocol-related medical issues

• Collaborate with project teams, sponsors, and regulatory authorities to ensure compliance with applicable standards and guidelines

• Support medical writing and regulatory documentation, including CSR review and safety narratives

About You

To be successful in this role, you will have:

• MD or equivalent medical degree with board certification (preferably in cardiology or internal medicine)

• Significant experience (8+ years) in the pharmaceutical/CRO industry, including Medical Monitoring responsibilities

• Demonstrated expertise in Cardiovascular clinical trials, across multiple phases (Phase I–IV)

• Proven ability to interpret complex clinical data and make sound medical decisions

• Strong communication and cross-functional collaboration skills

• Prior experience working in a CRO environment is essential

• Must be US-based and legally authorised to work as an independent contractor

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.

This is a flexible, contract-based opportunity to work with a global CRO on cutting-edge cardiovascular studies. You’ll collaborate with a dedicated team committed to advancing patient outcomes while enjoying autonomy and professional respect.

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.

Job Tags

Contract work, For contractors, Local area, Worldwide, Flexible hours,

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