Study Delivery Manager

ICON Strategic Solutions; A distancia; MXN 400,000 - 600,000; Jornada completa

Descripción de la vacante

A leading healthcare organization in Mexico is seeking a Clinical Trial Manager to oversee planning and execution of clinical trials. The role involves collaboration with diverse teams to ensure successful delivery and adherence to regulations. Candidates should have a university degree in medicine or science and experience in driving clinical deliverables. The position includes various health and retirement benefits, promoting a supportive work environment for all employees.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Formación

• Demonstrated ability to drive clinical deliverables.
• Subject matter expertise in the therapeutic area.
• Prior monitoring experience preferred.

Responsabilidades

• Plan and manage all aspects of clinical trials.
• Collaborate on clinical trial protocols and procedures.
• Build relationships with trial investigators.
• Ensure compliance with regulations and guidelines.
• Make decisions on trial design and risk management.

Conocimientos

Project management

Cross-functional collaboration

Problem solving

Compliance with regulations

Educación

University degree in medicine or science

Descripción del empleo

Home - Based - Mexico

ICON 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 development.

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross‑functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.

What you will be doing

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem‑solve and make critical decisions regarding trial design, vendor selection, and risk management.

Your Profile

• University degree in medicine, science, or equivalent combination of education & experience
• Demonstrated ability to drive the clinical deliverables of a study
• Subject matter expertise in the designated therapeutic area
• Prior monitoring experience is preferred
• Ability to travel up to 20%

What ICON can offer you

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
• Life assurance
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON employee? Please click here to apply.