Project Manager - In Vitro Diagnostics (Home Based)

Are you a seasoned Project Manager with experience in Diagnostics and Medical Device studies passionate about playing a key role in the overall management for global clinical research projects?

Location: Any US location (Home or Office Based)

Project Manager (In-Vitro Diagnostics) role at ICON:

As a Project Manager within our therapeutically aligned team, you will be expected to contribute towards a culture of business excellence with a focus on streamlining processes, adding value to the business and exceeding client needs.  You will be the primary point of contact for designated clinical projects, responsible for: delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, resource requirements and deliverables, risk migration strategies, associated action plan and issue resolution. 

As part of ICON’s dedicated Medical Device & Diagnostics Research team you will have an opportunity to be involved in providing strategic support and tactical solutions for traditional, in vitro diagnostic, and software devices clinical studies. The group combines the medical and regulatory device and diagnostic expertise with global clinical development and commercialization solutions.

Benefits of Working in ICON:

ICON provides Project Manager’s with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and many other incentives amongst an opportunity to grow your career within our PMO.

You would be joining us at the very right time – just when we won the Best Contract Research Organisation Award at the annual Scrip Awards 2017.

Role Requirements:

Bachelor’s Degree in medicine, science or equivalent degree and a qualification in Project Management or equivalent (PMI certification) is desirable. At least 2 years PM experience within clinical research is essential. Specific therapeutic experience in In-Vitro Diagnostics, Orthopedic/Spine, Cardiovascular devices and comprehensive knowledge of medical device GCP is essential along with excellent communication, planning, decision-making, negotiation, conflict management and time management skills.  Willingness to travel up to 25% as needed.

What’s Next?

Following your application, you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.