This is an exciting opportunity to join ICON
As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it.
With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
As a Manager Study Start up at ICON, you’ll work with coordination, execution, control and completion of Clinical Operations.
Ensure delivery and development of the Study Start Up team against key metrics. Work with Leadership to develop and grow capabilities, productivity, and quality.
We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
The role Provide direction and accountability for the operational Study Start Up teams and their delivery at regional and site level.
Resourcing, line management, training, functional delivery and input on discussions around quality and operational delivery measurements within the Clinical Operations group Conduct regular discussions with direct reports and lead team meetings at regional and manager team level.
Assist with training for SSU Managers and Associates as required. Contact for region in regard to operational questions and escalations.
Work with Director / Senior Director and / or VP Clinical Operations to communicate all critical issues, business growth opportunities, developing key relationships as well as providing input regarding budgeting discussions to drive productivity and quality within the region.
Drive overall delivery at site and regional level, through your operational team to drive execution of service, client satisfaction, quality and efficiencies.
Represent Clinical Operations at Sponsor and internal audits.
What you need Bachelor’s degree Minimum 6 years Study start Up, Clinical Research experience that includes a minimum 4 years relevant experience as a SSUA, Senior CRA or Principal CRA (in a Lead CRA role), or at least 2 years as a Project Manager, CRA / SSU Manager or equivalent job role.
Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent management skills, developed with a collaborative approach to driving performance and success in a global environment Direct experience managing SSUA’s / Clinical Research Associates is preferred
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer M / F / D / V and committed to providing a workplace free of any discrimination or harassment.