CRA I- Homebased
Talent Acquisition Team Lead
About the role
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Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP. Depending upon experience, become involved, when required, in other areas of study management and staff training and contribute to the review of ICON systems and procedures as appropriate. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.
Overview of the Role
- Travel (approximately 60%) domestic and/or international
- Expert knowledge of ICON Clinical Research SOPs/WPs, ICH, GCP and appropriate regulations.
- Expert knowledgeable of ICON systems.
- Maintain timelines. Ensure accuracy and completeness of data entered into ICON systems.
- Recruitment of investigators.
- Independent and proactive co-ordination of all the necessary activities required to set up and monitor a study, including the following:
- Identify investigators.
- Help, when requested, in preparation of regulatory submissions.
- Design patient information sheets and consent forms.
- Co-ordinate documents translation, verification and back translations where required.
- Ensure timely submission of protocol/consent documents/safety reports for ethics/IRB approval according to local requirements.
- 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 or designees 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.
- Ensure correct archiving of files on completion of a study.
- Maintain patient and sponsor confidentiality.
- Assume additional responsibilities as directed by Project Manager (PM).
- Responsible for the conduct/management of any aspect(s) of a project, when requested and authorized by a Project Manager.
- Act in a Lead role on a study, assuming additional responsibilities as detailed/documented by the Project Manager, if appropriate.
- Co-ordinate and/or participate in feasibility studies for new proposals, as require
- Identify investigators.
- Investigational Products (IPs) stored and managed by the site:
- Ensure storage conditions and acceptable supplies are provided
- Ensure IPs is 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.
- Ensure storage conditions and acceptable supplies are provided
- Be cost effective.
- Participate in training and mentoring new staff up to Clinical Research Associate level as appropriate.
- Participate in data listing reviews, as applicable.
- Assist with marketing the company if and when appropriate.
- Other duties as assigned.
Role Requirements / Skills / Experience Required
- Bachelor’s degree or equivalent in medicine, science or related discipline.
- Experience should include monitoring skills and understanding of field monitoring requirements
- Minimum of at least 1 year of experience with site monitoring
- Ability to review and evaluate clinical data.
- Computer literacy desirable
- Good oral and written communication skills.
Application process
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