Icon plc is a world-leading healthcare intelligence and clinical research organisationFrom 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 successIcon people have a mission to succeed and a passion that ensures what we do, we do well.
Responsibilities
Provides execution support to the real world evidence (rwe) team to initiate and execute site facing non-interventional studies conducted in the us and globally.
The pra non-interventional studies operations manager, in collaboration with the rwe study lead, will facilitate
Vendor identification
Vendor qualification
Vendor contracting oversight
Vendor cda requests
Oversight of site contracting and payments
Site id and selection
Irb documentation and approval
Patient privacy release form
Day to day vendor oversight and management
Ensure site training
Overall management of timelines, deliverables and budget
Rwe system update and qc
Request for proposals from approved vendors
Qualifications
Required experience:
Minimum education
An undergraduate degree.
Minimum experience
Minimum 3 years experience in clinical research, including a management role as a team lead or project manager experience.
Reads, writes and speaks fluent english; fluent in language of host country.
Preferred experience:
Minimum qualifications
Bachelor’s degree required
One (1) to three (3) years of experience in a pharmaceutical project management role
Drug development knowledge with basic to strong understanding of other functions relevant to the position which may include: research, pre-clinical, clinical, commercial, and regulatory
Strong interpersonal skills with experience leading cross-functional teams in matrix environment preferred.
Demonstrated operational and execution support for non-interventional studies
Understanding of ispor best practices for chart abstraction studies
Benefits of working in icon:
Our success depends on the knowledge, capabilities and quality of our peopleThat’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 programsIn 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 harassmentAll 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.
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