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Job ID 2114918
Job Description
Join a groundbreaking clinical research organization that leverages healthcare intelligence to drive innovation and improve patient outcomes. As a valued member of our team, you’ll play a pivotal role in numerous clinical trials across multiple therapeutic areas. Your Responsibilities:
Manage multiple clinical trials with a strong emphasis on quality of life, engaging in regional travel.
Exhibit leadership skills through active participation in special initiatives and mentorship for junior team members.
Take charge as Lead Site Manager, providing training to other Site Managers on study protocols.
Prepare essential site startup documentation, including the Site Initiation Visit agenda.
Represent the Site Manager’s perspective during the review of study documents, such as Monitoring Guidelines.
Act as a liaison for Local Trial Managers in study meetings and discussions.
Conduct comprehensive reviews of reports for sites assigned to other Site Managers within the same trial.
Support the development of country budgets and contract negotiations in collaboration with CCS colleagues.
Assist with the Aggregate Safety Visit process.
Contribute to the achievement of key performance indicators as outlined in the Quality Oversight Plan (QOP).
Key Collaborations:
Your primary collaborators will include the Provider Functional Manager, Clinical Trial Assistants, Local Trial Managers, and members of the Central Study Team for assigned clinical trials.
You will also work closely with the Study Responsible Physician, Regional Quality and Compliance Manager/Specialist, and site personnel such as investigators and coordinators.
Qualifications Required:
A Bachelor’s degree, RN, or equivalent in Biological Sciences or related field.
Must reside in Florida (Miami, Orlando, or Tampa) within proximity to a major airport.
2-3 years of pharmaceutical clinical trial monitoring experience is essential.
At least 2 years of experience monitoring in multi-therapeutic area trials.
Demonstrated knowledge across various therapeutic areas.
Experience in analytical and risk-based monitoring is advantageous.
Proven ability to implement effective patient recruitment strategies at assigned study sites.
Strong capability to collaborate with investigators and site staff to ensure adherence to study timelines.
Proficient in utilizing various clinical trial management systems and databases (e.g., CTMS, EDC, eTMF).
Exceptional communication and influencing skills for effective remote and onsite management of study sites.
A thorough understanding of Good Clinical Practice, ICH guidelines, and local regulatory requirements.
Willingness to travel up to 50% of the time.
Applicants must have legal authorization to work in the United States and will not require future sponsorship for employment visa status.
Why Choose ICON?
Your success is our priority. At ICON, we foster a diverse culture that celebrates high performance and nurtures talent. Alongside your competitive salary, we offer a comprehensive benefits package designed to promote your well-being and support work-life balance for you and your family.
Some of our benefits include:
Generous annual leave options.
Health insurance plans tailored to your and your family’s needs.
Robust retirement planning options for a secure financial future.
Access to the Global Employee Assistance Programme for 24/7 support.
Life assurance coverage.
Flexible benefits customized to your location, including childcare vouchers and gym memberships.
Explore the array of benefits waiting for you at ICON on our careers website. We are committed to cultivating a workplace where diversity, inclusion, and belonging are at the forefront of our mission. Your background and experience make you a unique candidate, and we encourage you to apply even if you don’t meet every requirement listed. You could be the perfect fit for this or other opportunities within ICON.