Latam Regulatory Submissions Lead: Study Start-Up

Job Summary:Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based **Regulatory Submissions Manager** to join our Study Start Up team in Mexico City!This position plays a key role in the study start up process at Medpace.If you want an exciting career where you use your previous expertise and can...

Study Start Up Associate II - Mexico - HomebasedICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Study Start Up Associate II...

A leading global healthcare company in Mexico City seeks a detail-oriented regulatory specialist to manage site start-up activities and documentation.This role involves coordinating regulatory submissions and maintaining compliance with ICH guidelines.Candidates should have a relevant university degree and a minimum of 2 years' experience in clinical...

Clincal Development CenterMéxicoAre you passionate about clinical trial management and regulatory excellence Do you thrive in an unordinary and dynamic environment where collaboration and innovation drive success If you have a strong background in clinical development and are ready to lead the way in ensuring seamless trial start-up activities we want to...

A leading biostatistics firm seeks a Senior Data Analyst with expertise in Real-World Evidence (RWE) to design complex statistical analyses and lead RWE study designs. This fully remote position calls for an experienced Biostatistician with advanced skills in programming and a strong background in regulatory submissions. Enjoy flexible schedules and a focus...

A leading fintech company seeks a Licensing Manager for LATAM to oversee regulatory licensing across Mexico and Brazil.The role involves managing licensing submissions and compliance, ensuring the company aligns with regional regulations.Ideal candidates will have 4–8 years of relevant experience, strong Spanish language skills, and a familiarity with...

Job Advert Posting- At ICON, it's our people that set us apart.Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.- ICON plc is a world-leading healthcare intelligence and clinical research organization.From molecule to medicine, we advance clinical research by...

At ICON, it's our people that set us apart.Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration,...

At ICON, it's our people that set us apart.Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.ICON plc is a world-leading healthcare intelligence and clinical research organization.From molecule to medicine, we advance clinical research by providing outsourced...

Job Summary:Join Medpace in Mexico!As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience.You will be a productive member of the team, and will be mentored and supported as you develop your skills.Working directly with Regulatory Submissions...