Project Manager, Feasibility Site Activation - Sr Project Manager, Feasibility Site Activation

ICON; San Antonio (TX); Remote; USD 80,000 - 120,000; Full time

Job summary

ICON, a leading healthcare intelligence organization, is looking for a Project Manager/Sr Project Manager to drive the activation of global investigative sites with a focus on quality and exceeding customer expectations. This role requires 3-6 years of experience in the Clinical Research environment and includes responsibilities such as managing site activations, coordinating internal teams, and ensuring compliance with regulatory processes. Join ICON to be part of a diverse culture that rewards high performance and supports employee well-being.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning offerings

Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• 3-6 years of experience in a Clinical Research environment, focusing on Start Up experience.
• Excellent written and verbal communication skills.
• Ability to work to tight deadlines.

Responsibilities

• Accountable for driving and accelerating the activation of global investigative sites.
• Lead studies with highest quality standards to exceed customer expectations.
• Act as customer point of contact for assigned studies; resolve study issues.

Skills

Project management

Excellent written communication

Excellent verbal communication

Understanding of regulatory processes

Ability to work to tight deadlines

Education

Bachelor’s Degree

Job description

Project Manager/Sr Project Manager, Feasibility Site Activation - Homebased - Mexico, Brazil, Colombia, Chile and Peru

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Role Summary:

Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality output, and exceeding sponsor expectations. Accountable for the overall coordination, implementation and completion of site activation or maintenance activities for assigned projects of work in line with ICON/sponsor SOPs as appropriate, including regulatory/ethics, site contracts, essential documents, and site activations. Interacts with internal teams and stakeholders, as well as sponsor teams and stakeholders as needed.

You will be doing:

• Lead studies with highest quality standards to exceed customer expectations.
• Review study and partnership budgets for proposals and sales as needed.
• Drive assigned studies to meet KPIs and delight customers and sites
• Act as customer point of contact for assigned studies; resolve study issues and drive exceptional customer delivery
• Represent FSA at audits and inspections
• Participate in Business Development opportunities to support the growth of the assigned portfolio, function, and/or region/country(ies)
• Travel (approximately 10% depending on country structure and direct report levels) domestic and/or international

Your profile:

• Bachelor’s Degree
• 3-6 years 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

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What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply