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Manager, Clinical EP

  1. San Antonio
JR115245
  1. ICON Full Service & Corporate Support
  2. Early Phase Services
  3. Office Based

About the role

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

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.




Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
• As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Travel (approximately 0%) domestic and/or international.
• *Coordinate with PI, Sub-PI, CRC Manager, CRC, and PM/SM to ensure proper execution of clinical trials by following all standard operating procedures and study protocols, as appropriate.
• Ensure proper documentation of data and dataflow of all clinical procedures through the quality control process.
• Participate in the quality control execution and review of study documents (e.g. source documents, informed consents).
• May function as a clinician as necessary, to ensure adequate coverage of scheduled clinical trials.
• Effectively manage resource capacity to ensure adequate coverage on projects.
• *Ensure staff complies with all applicable regulations (e.g. OSHA, FDA, etc.)
• *Assess training issues of staff and implement appropriate training while collaborating with appropriate IDS staff.
• Coordinate and lead monthly supervisors’ meeting or other meetings as appropriate.
• Carry out directives from PI and/or MD/VP, or the Director of Operations / Clinical Operations.
• To undertake other reasonably related duties as may be assigned from time to time.

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.  In addition, 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.

ICON, including subsidiaries, 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.

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Day in the life

A Journey of Growth and Excellence: An ICON Employee's Testimonial

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Our People

Content type

Blogs

Publish date

10/02/2023

Summary

An Evolution of Progress and Success: Zashan's story a Clinical Research Associate (CRA) Having a satisfying career involves finding a company that prioritizes progress, improvement, and chances f

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Zashan, who began his journey with us in 2016, has shared his experience and insights.

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Who we are

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