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Site Activation Lead/Sr. Site Activation Lead job in Salt Lake City at ICON Clinical Research

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Site Activation Lead/Sr. Site Activation Lead at ICON Clinical Research

Site Activation Lead/Sr. Site Activation Lead

ICON Clinical Research Salt Lake City, UT (On Site) Full-Time

ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.

Site Activation Lead

As a Site Activation Lead at ICON, you would advance clinical trial start-up activities by understanding the client objectives and assist in the development of the plan for country and site distribution. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

Role Summary

Lead clinical trial start-up activities by understanding the client objectives and assist in the development of the plan for country and site distribution

Oversees day to day delivery of all aspects of site activation in the projects assigned.

Ensures that each project has a site activation plan and that the study is being conducted in accordance with that plan and in an effective manner which meets sponsor timelines and expectations and is in compliance with ICON/client KPIs, ICON/client SOPs, reporting norms, appropriate regulations and ICONs quality standards

Lead sponsor initiatives such as kick-off meetings, bid defenses, project update and status calls, and other communications

Utilize project management skills to optimize performance and collaboration to ensure successful study outcomes

*Travel (approximately 15%) domestic and/or international. Anticipated activities may include attendance at Bid Defenses, Kick-Off, Investigator or study team meetings.

What you need for a Site Activation Lead

Bachelors Degree preferably in life sciences

Minimum of 5 year of experience in a Clinical Research environment, focusing on Start Up experience

Project management skill set

Understanding of regulatory and submission processes in many different countries

Excellent written and verbal communication

Ability to work to tight deadlines

Sr. Site Activation Lead

As a Senior Site Activation Lead at ICON, you are accountable for driving and accelerating the activation of investigator sites. Additionally you will be accountable for the implementation and completion of site activation activities for global, complex projects. As a Senior Site Activation Lead you will work cross functionally throughout ICON and with ICON sponsors, ensuring a positive customer experience throughout the relationship!

The role

Primary SSU point of contact for designated global projects and programs

Accountable for developing successful sponsor relationships, proven through consistently high sponsor satisfaction scores in SSU, contributing to the retention and repeat business.

Working cross-functionally to ensure sites and countries optimize accelerated delivery of the project

Risk management and mitigation strategies within site activation to ensure timely delivery

Ensure stringent oversight of project in terms of timely and quality delivery of key landmarks

Accountable for management of sponsor expectations and ensuring compliance with ICON / Sponsor critical metrics; SOPs; and quality standards.

Responsible for the study start up budget, including resources; timelines; rates and margins.

*Travel (approximately 15%) domestic and/or international. Anticipated activities may include attendance at Bid Defenses, Kick-Off, Investigator or study team meetings.

What you need for a Sr. Site Activation Lead

Bachelors Degree preferably in life sciences

In depth proven experience within clinical research, specifically in the clinical studies regulatory environment.

Excellent Leadership skills, developed with a collaborative approach to driving performance and success

Experience in successful management and delivery of study deliverables, ideally with proven experience in the oversight of project management and staff in a multi-country / global environment.

Cross functional leadership and influencing skills

Strong planning and organization skills within a time pressured environment.

Excellent written and verbal communication, fluent in English

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. Thats 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.

#LI-KC1

#REMOTE

Recommended Skills

  • Clinical Research
  • Clinical Trials
  • Communication
  • Coordinating
  • Customer Experience
  • English
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