Freelance Clinical Research Associate - Netherlands

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Job description

*Senior Clinical Research Associate *

Rachel Musk has a fantastic opportunity available as the Senior Clinical Research Associate of a growing yet global European CRO specialising within Oncology.

This is a great opportunity for an experienced monitor to work within an innovative organisation with huge potential whilst also having time available for other external projects.

Working within Early Phases you will be expected to have strong experience in Phases I & II, and the tasks that come with this.

You will also be expected to hit the ground running at a minimum of 0.6 FTE (3 days per week)

With a high standard of work throughout the contract, there will be the potential for multiple future extensions.

Are you experienced within the clinical industry?

Have you got what it takes to succeed?

Do you need a new challenge in your life?

Do you want to be recognised for your hard work?

Do you have extensive experience as a CRA?

Yes, to any of the above? *Apply now! *

This role is based in the Netherlands

You will need to review regulatory documents and prepare site reports.

You will be responsible for multiple projects and must be willing to work as part of a team.

You will be expected to perform regional travel at 75%.

This will be 0.6 FTE on a 12-month contract, with the opportunity to extend.

You will work in the following therapeutic areas: - Oncology

*Have you got what it takes?*

*Responsibilities;*

* Full protocol ownership, acting as the key point of contact between Sponsor and site investigators

* Site selection, initiation, feasibility and close out

* Independent site monitoring

* Assisting the study Clinical Project Manager (CPM) in updating study metrics, compiling status reports

* Create and review informed consent, study reports and monitoring tools

* Interact with project team regarding objectives and status of clinical projects

* Ensure regulatory compliance with FDA, ICH/GCP guidelines and company SOP's

* Perform site inspections independently

* Monitor patient safety on-site

* Perform site initiation visits

* Monitor and maintain ICH-GCP compliance

*Experience;*

* University degree in health-related field

* Strong CRA experience within the infectious disease field

* Strong operational, organizational, presentation, documentation and interpersonal skills

* Self-starter requiring minimal supervision

* Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements

* Willingness and ability to travel

* Fluency in English is required

* Advanced computer skills (Internet, Microsoft Office)

Contact me on*:*

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*Or Ryan* on **