Regulatory & Start-Up Specialist – Clinical Trials (Mexico)

A leading clinical research organization in Mexico City is seeking a Regulatory Submissions Manager to oversee the start-up process for clinical trials. This office-based role requires at least 4 years of relevant experience, strong communication, and leadership skills. Ideal candidates will manage global start-up activities and ensure the quality of...

A leading clinical research organization in Mexico City is seeking a Regulatory Submissions Manager to oversee the start-up process for clinical trials. Candidates should have at least 4 years of relevant experience with strong communication and leadership skills. The role is office-based with a focus on managing global start-up activities and ensuring the...

A leading clinical research firm is seeking a Contract Specialist in Mexico City to develop global contracting strategies and support start-up activities. The ideal candidate should have at least 5 years of experience in clinical site contracting with strong negotiating and communication skills. Responsibilities include collaborating with sponsors, providing...

A leading clinical research organization in Mexico City is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role. This position is crucial for the study start-up process, requiring a bachelor's degree in life sciences and at least 4 years of relevant experience. Candidates should be fluent in English and the local language...

A leading clinical research organization is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role in Mexico City. This position is crucial for the study start-up process, requiring a bachelor's degree in life sciences and at least 4 years of relevant experience. Candidates should be fluent in English and the local language...

A leading clinical research firm in Mexico City is seeking a Contract Specialist to develop global contracting strategies and support start-up activities. The ideal candidate should have at least 5 years of experience in clinical site contracting, with strong negotiating and communication skills. Responsibilities include collaborating with sponsors,...

A leading clinical research firm in Mexico City is seeking a Contract Specialist to develop global contracting strategies and support start-up activities. The ideal candidate should have at least 5 years of experience in clinical site contracting, with strong negotiating and communication skills. Responsibilities include collaborating with sponsors,...

Study Start Up Manager Join Medpace as a full‑time, office‑based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‑up process, building on your experience in clinical trials and regulatory submissions. You will use your expertise to develop and grow your career while supporting our LATAM clinical trial...

Study Start Up Manager Join Medpace as a full‑time, office‑based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‑up process, building on your experience in clinical trials and regulatory submissions. You will use your expertise to develop and grow your career while supporting our LATAM clinical trial...

A clinical research organization in Mexico City is seeking a Regulatory Submissions Coordinator to support Regulatory Submissions and gain vital experience in study start-up. Responsibilities include providing support activities, ensuring compliance, and conducting document quality control. Requirements include a Bachelor's degree in Life Sciences, 1-3 years...