Clinical Trial Job at ICON plc in Mexico
ICON plc is seeking a Global Clinical Associate to join its Clinical Operations team in Mexico City. This remote opportunity at ICON plc Careers allows professionals to contribute to global clinical trials, supporting the design, implementation, and management of innovative treatments and therapies. Join a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development for a Clinical Trial Job in Mexico.
Job Details:
- Job Title: Global Clinical Associate
- Job Reference: JR144513
- Location: Mexico City
- Department: Clinical Operations – ICON Strategic Solutions
- Work Type: Remote
- Industry: Clinical Research / Healthcare Intelligence
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company is dedicated to driving innovation and excellence in clinical development while fostering an inclusive and diverse work environment.
ICON plc partners with pharmaceutical, biotechnology, and healthcare organizations globally to accelerate the development of life-changing treatments. The company prioritizes high performance, professional growth, and a culture of inclusion and belonging.
Educational Requirements:
- Bachelor’s or advanced degree in Life Sciences, or a related field
- Previous global experience in clinical research or healthcare preferred
- Experience within the pharmaceutical, biotechnology, or CRO industry is advantageous
Key Responsibilities:
- As a Global Clinical Associate, you should assist in the planning, execution, and monitoring of clinical trials
- Ensure adherence to protocol requirements, regulatory guidelines, and industry standards
- Coordinate study activities, including site initiation, patient recruitment, data collection, and monitoring visits in this Clinical Trial Job at ICON plc Careers
- Collaborate with cross-functional teams, including Clinical Operations, Data Management, and Biometrics
- Maintain comprehensive study documentation and records in compliance with regulations and SOPs
- In the Clinical Trial Job, you should support study close-out activities, including data cleaning, analysis, and preparation of clinical study reports
Skills Required:
- Strong organizational and time management skills
- Ability to prioritize tasks and manage competing priorities effectively
- Excellent attention to detail and problem-solving abilities
- Commitment to ensuring data accuracy, integrity, and compliance
- Effective communication and interpersonal skills
- Ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites
Benefits of the Clinical Trial Job:
- Competitive salary package
- Country-specific comprehensive health insurance offerings
- Competitive retirement planning options
- Global Employee Assistance Programme (LifeWorks) with 24-hour access to specialized professionals
- Life assurance coverage
- Flexible optional benefits such as childcare vouchers, gym memberships, travel passes, and health assessments
- Inclusive and accessible workplace culture focused on diversity and belonging
