Clinical Team Manager 3

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. ResponsibilitiesWhat will you be doing?
As a Clinical Team Manager (CTM), you have a wide range of responsibilities. We’re including a few of the big ones. Primarily, you will work to achieve the most successful clinical trial possible. You will lead cross-functional teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitigate, and escalate risks or issues when necessary.

• Provide Project Oversight and Leadership for Clinical Deliverables
• Project Resourcing
• Quality – Training & Development
• Project Finance
• Customer Relations (Internal & External)

Qualifications
What do you need to have?
Level 3:

• 
  Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse); or equivalent work experience, required
• 7+ years of clinical research experience, required

• 4-5+ years of experience in clinical trial management, strongly preferred
• 2+ years monitoring experience, strongly preferred
• Experience in managing complex or global trials, preferred
• Minimum 1 year oncology experience, preferred
• Experience in managing all trial components (start-up to database lock), preferred
• Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferred
• Experience in managing complex trials or global trials, preferred

• English fluency (ability to read, write, speak), required
• Travel of up to a maximum of 30%, required
• To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

LOCATION: This position may be home-based or office-based, depending on location.
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.
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