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Clinical Research Associate II

hace 2 meses

Xico, México Icon A tiempo completo

**About ICON**

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations.

**Our Mission**

We put our patients at the center of everything we do, helping to accelerate the development of drugs and devices that save lives and improve quality of life.

**Our Culture**

Our people are our greatest strength, and they are at the core of our culture. We are a mission-driven organization with a passion for excellence, and we strive to make a positive impact on the world.

**The Role**

We are seeking a highly skilled and motivated Clinical Research Associate II to join our team. As a member of our team, you will be responsible for:

  • Recognizing, exemplifying, and adhering to ICON's values, which center around our commitment to People, Clients, and Performance.
  • Embracing and contributing to our culture of process improvement, with a focus on streamlining our processes and adding value to our business and meeting client needs.
  • Working on study teams that are often virtual, multi-cultural, and multi-disciplinary.
  • Serving as the primary contact for sites and investigators participating in studies.
  • Acting as a resource for internal study teams and other ICON departments.
  • Maintaining, reviewing, and ensuring the adequacy of information and data contained in site management reports, tracking systems, and other site management documents.
  • Conducting and completing remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan.
  • Participating in QA audits as needed.
  • Regularly attending and contributing to project-specific and departmental meetings.
  • Ability and willingness to travel as needed (drive and fly) - approximately 25% of the time.
  • Reviewing drug storage and drug accountability procedures (as applicable), in accordance with applicable SOPs.
  • Maintaining and archiving study documentation and correspondence, as needed.
  • Assisting with site contracting process, as needed.

**Requirements**

To be successful in this role, you will need:

  • Excellent written and oral skills.
  • A Bachelor's degree in Life Science (BS is a mandatory).
  • Minimum 1 to 3 years of experience in Clinical Research.
  • Strong administrative skills.
  • Organization skills to support several team members.

**Benefits of Working at ICON**

We offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, as well as a wide range of variable pay and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now and into the future.

**Equal Opportunities**

ICON, including subsidiaries, is 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.