Join to apply for the Senior Medical Monitor, USA/LATAM role at Emerald Clinical
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 the US or LATAM.
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.
- 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?
- Purpose‑Driven Work : You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
- General 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
- 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.
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