ICON

Project Manager

Romania, Bucharest Full time
Regional Clinical Study Manager - Remote - Romania or Bulgaria

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

We are currently seeking a Project Manager to join our diverse and dynamic FSP team.

In this role, you will be responsible for regional study delivery in Romania, Bulgaria, Czech Republic and Moldova. You will lead the regional clinical operations team (including oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned studies.

What You Will Be Doing:

  • Leading the regional clinical operations team effectively and act as point of escalation for resolution of issues within the region for the assigned studies

  • Leading external vendors involved in study delivery on a regional level

  • Planning and management of the assigned clinical studies from feasibility through closeout activities for region, in line with global study timelines

  • Ensure that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders

  • Providing regional input on global study plans

  • Collaborating closely with CRAs in the region to ensure proper study execution at the sites.

  • Review and signs-off of monitoring reports

  • Monitoring study activities in region to ensure compliance with the study protocol, SOPs, ICH/GCP and all other relevant regulations

  • Working with the sourcing team to select and manage regional study vendors

  • Managing regional study budgets

Your Profile:

  • University Degree in a scientific or healthcare discipline required, 

  • 4 or more years of progressive experience in clinical research within biotech, pharma or CRO industry

  • Strong experience in managing oncology studies is required

  • Proven experience in clinical research including relevant experience as team lead in clinical functions

  • Prior experience as CRA

  • Computer Skills:     MS Office, Project Planning Applications

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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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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