Company Description:
Ergomed PLC is a rapidly expanding, full-service mid-sized Contract Research Organization (CRO) specializing in Oncology and Rare Diseases. Since its founding in 1997, the company has grown steadily through strategic investments and acquisitions, with operations across Europe, North America, and Asia.
At Ergomed, we foster a culture of visibility, creativity, and career development, giving employees a voice in shaping the company’s future. Our international culture thrives on collaboration, and we place great importance on employee well-being and mental health, understanding that a healthy work-life balance is key to high-quality service and client satisfaction.
Join us in our mission to make a positive impact on patients' lives.
Job Description:
Ergomed is looking for experienced Regulatory Affairs professionals with expertise in managing complex global clinical studies. This opportunity is open to candidates worldwide, but applicants must have excellent English communication skills and a strong understanding of the clinical trial environment and ICH GCP.
Key Responsibilities:
Qualifications:
Additional Information:
At Ergomed, we prioritize diversity, equity, and inclusion by fostering an equal-opportunity workplace where individuals from all backgrounds, genders, and ages can thrive. We believe that our people are our greatest strength, and by working together with a human-first approach, we continue to improve the lives of those we serve.
What We Offer:
#LI-Remote
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