Study Start Up Associate I-biotech - Ciudad de México - ICON

ICON

Empresa verificada

Ciudad de México

hace 2 semanas

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

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.

Join Our Study Start Up Team and Help Shape the Future of Clinical Trials

Are you ready to make a difference in the world of medical research? We are seeking dedicated individuals to join our team and play a crucial role in preparing physicians at research sites for groundbreaking clinical trials.

As a member of our dynamic team, you will:

Coordinate, balance, and facilitate activities to ensure the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01), in line with ICH GCP guidelines and all relevant regulations.
Champion quality, efficiency, and cost containment in the study start up process for a specific region or subdivision within the CDP group.
Gain invaluable mentorship from our experienced Mgr/Sr. Manager
Central Services or Designee.

What you need to bring to the table:

High school diploma or local equivalent.
Bachelor's Degree in Life Sciences preferred.
Minimum of 1 year of experience or understanding of clinical study start up requirements and activities.
Proven experience in clinical trial operations and adherence to regulatory guidelines.
Proficient project management skills.
Read, write and speak English fluently

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.

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