Worldwide seeks a senior Regulatory Affairs professional to lead global submissions across EMEA, APAC and LATAM, ensuring compliance with evolving regulations. The role involves coordinating ethics submissions, supporting business development, and mentoring junior staff in a fast-paced, multinational environment.
The candidate will provide expert regulatory advice, prepare technical documents like IMPDs and IBs, and liaise with sponsors, project managers, CRAs and Medical & Scientific Affairs
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EMEA Regulatory Affairs Manager — Remote employer: Worldwide Clinical Trials
Worldwide Clinical Trials is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals passionate about clinical research. With a strong emphasis on employee growth, the company offers numerous opportunities for skill development and career advancement, all while working in a diverse environment that values creativity and teamwork. Located in a vibrant area, employees benefit from a supportive atmosphere that encourages meaningful contributions to patient engagement activities.
