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
What will you be doing?
Perform quality and auditing activities to assess compliance with corporate policies, industry standards, and applicable regulationsThis includes conducting a variety of audit activities which may include, but not be limited toInternal process audits, pharmacovigilance audits, study specific audits (e.gInvestigator site, in process, pharmacy/distribution, trial master file), and audits of vendors used to support icon servicesProvide gcp consultation to the icon organization
Level 2 auditor independently conducts the following activities as assigned by quality & compliance (q&c) management:
Performs contracted, routine and complex audits according to client expectations and/or icon sopsOften assigned to act as audit lead for a team of auditors and/or to conduct complex audits independently
Plans and ensures audits are scheduled.
Conducts audits to assess adherence to protocols, sops, regulations, gcp, and expectations for data accuracy and completeness.
Reports observations/findings according to client or icon sops and report templates within defined timelines.
Tracks, collects and issues responses and corrective actions according to client or icon sops.
Documents closure of audit
Interprets regulations and guidance documents governing gcp and provides the interpretation to icon staff and clients.
Facilitates client audits and regulatory inspections of icon.
Participates in q&c projects such as management of issue escalations, capa projects, or other q&c initiatives.
Qualifications
Requirements
Read, write and speak fluent english.
5+ years experience working in a clinical, regulatory, pharmacovigilance, or quality environment within cro/ pharmaceutical / healthcare industry.
Excellent verbal and written communication skills and interpersonal skills.
Excellent organizational skills.
Must possess a technical knowledge that is applicable to clinical drug development.
An undergraduate degree, its international equivalent in the sciences, technology, auditing, etcFrom an accredited institution or sufficient previous experience in auditing is required
Extensive experience in investigator site, vendor, and process audits.
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.
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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