Clinical Research Coordinator

hace 4 horas


Xico, México Icon Plc A tiempo completo

At Icon Plc, we believe our people are our greatest strength. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.

We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations. Our focus is on accelerating the development of drugs and devices that save lives and improve quality of life.

The Study Start Up Team plays a vital role in our operations. As a member of this team, you will be responsible for coordinating and facilitating activities related to the completion of Critical Document Package (CDP) and the IP release checklist in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, and sponsor requirements.

To succeed in this role, you will need:

  • Bachelor's Degree in Life Sciences
  • Minimum of 1 year's experience or understanding of clinical study start up requirements and activities
  • Experience of Clinical Trial operations and meeting regulatory guidelines
  • Knowledge of Informed Consent Forms
  • Proficient project management skills
  • Excellent communication skills in English and Spanish

We offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay and recognition programs, and best-in-class employee benefits, supportive policies, and wellbeing initiatives tailored to support you and your family at all stages of your career.

We are an equal opportunity and inclusive employer 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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