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• Recognize, exemplify and adhere to ICON"s values which center around our commitment to People, Clients and Performance. • As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. • *Ability and willingness to travel at least 60% of the time.(lnternational and domestic : fly and drive) • *Expert knowledge of ICON's SOPs/WPs, ICH, GCP and appropriate regulations. • *Familiarity with ICON systems . • *Maintain timelines . Ensure accuracy and completeness of data entered into ICON systems. • Recruitment of investigators . • *Independent and proactive coordination of all the necessary activities required to set up and monitor a study , including but not limited to the following : Identify investigators. Help when requested , in preparation of regulatory submissions . Design of patient information sheets and consent forms . Ensure timely submission of protocol/consent documents for ethics/IRB approval. Pre study/placement and initiation visits. Conduct regular monitoring visits in accordance with the ICON site monitoring SOP/sponsor site monitoring SOP, as appropriate Maintain all files and documentation pertaining to studies . Motivate investigators in order to achieve recruitment targets. Complete accurate study status reports. Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs. Keep the Project Manager regularly informed. Process case record forms to the required quality standards and timelines . Deal with sponsor generated queries in a timely manner. Ensure the satisfactory close-out of investigator sites . Participate, if requested, in the preparation of and review of study documentation , e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report. Participate in feasibility studies for new proposals as required. Ensure correct archiving of files on completion of a study . Maintain patient and sponsor confidentiality . Assume additional responsibilities as directed by the Project Manager. - lnvestigational Products (IPs) stored and managed by the site: • Ensure storage conditions and acceptable supplies are provided • Ensure IPs are supplied only to eligible patients • Ensure IP receipt, use and return are controlled and documented • Ensure disposition of unused IP comply with regulatory requirement and are in accordance with the sponsor. • *Act in a lead role on a study assuming additional responsibilities as detailed/documented by the Project Manager if appropriate . • Participate in data listing reviews, as applicable . • *Responsible for cost effectiveness • *Participate in training and mentoring new staff up to Clinical Research Associate level as appopriate. • Assist with marketing the company if and when appropriate . Other duties as assiQned .

Application process

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List #1

Day in the life

Shining a Light on Endometriosis Awareness Month

Teaser label

Inside ICON

Content type

Blogs

Publish date

04/18/2024

Summary

Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis

Teaser label

Endometriosis Awareness Month sheds light on this often-misunderstood condition affecting millions worldwide.

The Role of Data Management in Clinical Trials

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Industry

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Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials

Teaser label

This blog examines the critical role of data management in clinical trials.

Navigating the Clinical Research Supply Chain

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Industry

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Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ

Teaser label

Discover the intricate workings of the clinical research supply chain in this comprehensive guide.

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Global Business Services

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CRA II

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

Application process

Who we are

Government and public health services

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CRA II

Send me a message

About the role

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

ICON and you

ICON history

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Women in IT

Application process

Who we are