CRA II

ClinicalPro is seeking a CRA II for a leading CRO located in the USA.

This individual will be responsible for working with the Clinical Operations team. CRA II will support all research-related operations.

Must be eligible to work in the USA.

Responsibilities

• Management of designated investigational research sites, including prestudy, commencement, monitoring, and study close-out site visits, is the main responsibility.
• Produce, modify, distribute, and/or keep track of project-specific paperwork as required.
• Participate in the Trial Master File’s upkeep.
• Knowledge in electronic project management and documentation system.
• Keep in contact with the research locations, sponsor, and other stakeholders in the project to ensure effective communication and project progress.
• To stay as up-to-date as feasible in linked fields, organise training exercises and/or take part in them as necessary.
• Assist in the creation of, take part in the revision of, and attend training sessions for industry standard operating procedures

Skills and Requirement

• Biological science, life science, or any other healthcare-related area bachelor’s degree (or it’s equivalent) as a minimum.
• 3 years of relevant experience in a healthcare context.
• A comparable mix of education, training, and experience.
• Clinical trial monitoring experience of two years is necessary.
• It is preferred to have a recognised CRA Certification.
• Understanding of FDA laws and ICH-GCP standards.
• Strong communication abilities.
• Ability to function well in a group setting.
• Strong planning and organisational abilities.
• Excellent communication and professional abilities.
• Excellent time management abilities, including the capacity to multitask and order tasks.
• Self-driven and focused on the details.

Apply

If you’re interested in this position, apply now to send us an updated copy of your CV, or give us a call right away.

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