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Study Start Up Associate II

US-Pennsylvania-North Wales; UK-London
Permanent
Reference: 056787
This vacancy has now expired.
Description
Experienced Study Start Up Associate – Centralized Informed Consent Team
Location: anywhere EMEA , with Business level or native English
Must Have -  An informed consents experience. Preferably in creation of Study level ICFs, but at a minimum the creation of country/site ICFs.
 
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?
 We are looking for passionate, resilient, and inspiring individuals to join our team. As a member of the Study Start-Up Team, you will play an integral role in coordinating clinical trial start-up activities and serve as the primary contact for investigators and research coordinators in corporate sponsored human clinical trials.
 
Responsibilities:
Development and Authoring of study level informed consent masters in accordance with client specific requirement Liaising with ICON and sponsor study teams where required Review and approval of country and site level informed consent in accordance with client specific requirements.
Ensuring any legal or sponsor mandatory text requirements are adhered to Provide guidance and leadership to the study team in relation to Informed Consent process and development Ensuring timely review and tracking of consents to meet established study timelines and required metrics Involvement in the development of sponsor and ICON specific guidance and trainings Other duties or tasks as requested
 
What you need
·         A high school diploma or local equivalent
·         Bachelor’s Degree preferably in Life Sciences
·         Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities.
·         Experience of Clinical Trial operations
·         Experience meeting regulatory and ICON guidelines
·         Proficient project management skills.
 
 
Why join us?
On-going development is vital to us, and as a member of our team you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set.  We offer a very competitive salary and benefits package that includes an excellent retirement plan, health coverage, paid time off, income protection insurance programs, and staff recognition schemes.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 
EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin
 
 MH1#
 
 
 
 
 
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