Scientific Leadership Research Coordinator (Slrc)

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.
What will you be doing?
The Scientific Leadership Liaison is responsible for the coordination of scientific engagements and Investigator Studies Program (MISP) activities in support of the Global Scientific Affairs team.
What do you need to have?

• 5+ years of clinical research experience required, including at least 2 years experience in clinical trial management
• Facilitate review of final study report and submit abstract/manuscript to committee and databases
• Supported the Global Scientific Affairs Team for the therapy area assigned and activities surrounding scientific leadership strategy which drove post-marketing and clinical research initiatives
• Managed Global Scientific Affairs budget and reported financial status monthly.
• Managed Investigator Initiated Studies Program from study initiation to study completion.
• Managed and executed Scientific Input Engagements and Global Therapeutic Expert Forums (Investigator Meetings) for the Therapy area assigned in compliance with all US and International government regulations.
• Ensure clinical studies have IRB/IEC approval and are registered on the CTDB.
• Facilitate, review and negotiations of clinical and pre-clinical study designs, budgets, timelines, grant agreements.
• Read, write and speak fluent English; fluent in host country language required.
• Track and manage all documents via a global website and database for the Global Scientific Affairs team
• Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives preferred
• Coordinate with the Global Operations Specialist regarding CDAs, study budgets, contracts, approval of payments to investigators/institutions, forecasting and budgetary spending.
• Will require strong Power Point and Excel experience and the flexibility to travel on occasion.
• Experience in managing all trial components (start-up to database lock) preferred
• Assist with analysis of the content of each study application and check for completeness: budget, timelines, publication plan
• Responsible for fostering relationships with internal and external partners to encourage study teams to move forward during difficult times of transition within the company
• Coordinate activities with the investigators and country point of contact to ensure approved studies are initiated, followed-through, and completed within the time frame agreed upon according to the executed study agreement
• You will be the primary point of contact to ensure the committee decisions are communicated and document according to SOP
• Liaise with World Wide Regulatory Coordination to ensure appropriate documentation is obtained for clinical drug supply needs
• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.

Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.