Study Start Up Associate (Informed Consent Form) - homebased job in

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ICF (Informed Consent Form) Reviewer -- Study Start Up Associate I /II / Sr.

Do you have experience reviewing and negotiating language in Informed Consent Forms? If so, we have a career opportunity in the exciting world of drug discovery for you.

We are looking for someone with Informed Consent Form review experience (ICF Reviewer) to join our Study Start Up group. Our Study Start Up associates are integral in ensuring that physicians at research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.

As a Study Start Up Associate at ICON working as an Informed Consent Form Reviewer your main role is to review Informed Consent Forms and negotiate language as needed. You will assist in the drafting of ICF country templates for the United States and Canada, which are then distributed to study sites to make edits depending on their local IRB requirements and SOPs. You will review and negotiate these changes and potentially liaise with other stakeholders like the sponsor, legal, or the clinical team to ensure that changes to the ICF are acceptable.

We are looking for associates who have a background in clinical research at a CRO, Pharmaceutical company, study site, or who have worked at an IRB. Your experience must include performing ICF review as an essential function of the job. A bachelor’s degree in the life sciences is preferred.

We are a company of 13,500 employees in forty countries globally. We differentiate ourselves by developing innovative solutions to bring life-saving drugs to market faster and in a more cost-effective way to foster better patient outcomes. We are a top five clinical research organization with solid earnings and growth potential. Our belief in excellence is our core value in all that we do for our sponsor partners and the patients that we serve. As a company we strive to exceed our customers’ expectations in drug development solutions.

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.

A better career. A better world. A better you.

Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader.
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Study Start Up Associate (Informed Consent Form) - homebased

About the role

This vacancy has now expired. Please see similar roles below...

ICON and you

ICON history

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Benefits & Rewards

DE&I

Environmental, Social & Governance

Women in IT

A better career. A better world. A better you.

Who we are

Government and public health services

Why icon? full service mean for you?

Study Start Up Associate (Informed Consent Form) - homebased

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About the role

This vacancy has now expired. Please see similar roles below...

ICON and you

ICON history

Career Pathways

Benefits & Rewards

DE&I

Environmental, Social & Governance

Women in IT

A better career. A better world. A better you.

Who we are