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5I
Project Associate (Entry level)
520 ICR Mexico - MEX · Mexico City, Mexico
About The Role
- Project Associate - Mexico, Mexico City Hybrid: Office/Remote
- ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
- As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
- Location: Mexico Hybrid - 3 Days at Office / 2 Homework
Join our supportive, globally integrated team as a Project Associate. You’ll be pivotal in streamlining Standard Operating Procedures (SOPs), enhancing training compliance, and driving continuous process improvements—all while enjoying a balanced and rewarding work-life environment.
About the role
Key Responsibilities
SOP Management & Harmonization
- Coordinate SOP updates, reviews, and approvals efficiently.
- Track and report SOP progress, ensuring alignment with global practices.
- Integrate continuous improvement initiatives into SOPs effectively.
Training Coordination & Compliance
- Maintain optimized, compliant training plans.
- Collaborate with managers to update training modules and curricula.
- Manage training compliance tracking, issue regular reminders, and support audits with accurate records.
Continuous Improvement Coordination
- Coordinate proposed process enhancements, supporting streamlined and efficient workflows.
- Coordinate meetings and facilitate cross-team communication for SOP and training improvements.
- Other duties and projects as assigned.
Yor profile
- Advanced English proficiency (written and verbal).
- Bachelor’s degree completed, preferably in Life Sciences, Quality Management, Business Administration, or a related field.
- 6 months to 1 year of experience in training coordination, SOP administration, document control, continuous improvement, or a related function within the pharmaceutical, CRO, biotechnology, or other regulated industries.
- Strong proficiency in document management systems and the Microsoft Office Suite (Word, Excel, PowerPoint).
- Excellent organizational, communication, and interpersonal skills, with strong attention to detail.
- Working knowledge of Good Laboratory Practice (GLP) regulations and quality requirements.
- Experience supporting or participating in continuous improvement initiatives and process optimization projects.
- Strong analytical, problem-solving, and project management skills, with the ability to manage multiple priorities and meet deadlines in a fast-paced environment.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Benefits may vary depending on role and location.
- Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
- ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
- If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
- Are you a current ICON Employee? Please click here to apply
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