Senior Clinical Associate

JR112843

Senior Clinical Associate (Project Support Assistant)

Mexico City

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, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Overview:

The Senior Clinical Associate (Project Support Assistant) is responsible for assisting the GSM and AGSM within the Trial

Operations Study Team, dedicated to a Therapeutic Area BU or across one or more Units

Support with Global Trial initiation, Conduct and Reporting of Trial Progress, by coordinating and

performing assigned Operational Activities

Able to proactively identify and propose solutions to operational activities and work autonomously.

Responsibilities:

• Maintenance and update of the study e-room
• Responsible for the study tracking activities. CTMS updates for: study supplies, IP, budget, study metrics, patients’ status, deviations, compliance with systems use, etc.
• Support the communication to the Study team: Key trial information, Study Team Meeting Minutes, Newsletters, etc.
• Preparation and shipment of study ancillary supplies
• Keep regular communication and assist the Monitoring Team and the Study Vendors, following GSM instructions
• Support the GSM to coordinate the logistics of the CRAs’ training and the Investigator Meetings preparation: Registration forms, invitations, etc.
• Filling: collection, maintenance and archiving of essential study documents

What you will need to have:

Education: Bachelor’s degree in science

Knowledge and experience of working in a clinical trial environment.

Advanced English to Speak, Write and Read

Desirable 2 or 3 years of exp. with Clinical Research

Experience as Senior CTA (Clinical Trial Assistance)

Knowledge of ICH/GCP principles

NOTE: The position will be office-based (hybrid model). You can work 2 days at home per week.

Benefits of Working in ICON:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and 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 through the form below.

#LI-FB1