CRA

I am working with a European healthcare organisation who create cutting-edge products and applications for clinical research, patient-centred healthcare, market access, and public health.

The ideal candidate for this role will have the chance to collaborate with other skilled CRAs to gain knowledge of all clinical evaluation and regulatory issues as well as practical experience using ISO guidelines for the development of medical devices and the ICH guidelines for the development of drugs.

I would love to hear from seasoned CRAs as well as recent graduates in scientific fields, providing that they possess the necessary language abilities. There will be thorough instruction in the company's SOPs and clinical research protocols, as well as opportunities to observe more seasoned team members in action.

I am looking to recruit a CRA that speaks one of the following languages fluently: Polish/German/Dutch/Nordic Languages alongside advanced English, and French.

The ideal candidate would possess the following preferred abilities, credentials, and experience:

• A Bachelor's or Master's degree in Life Sciences
• Although not necessary, some early clinical research or training experience is preferred
• Polish fluency, advanced English, and French,
• Excellent communication and interpersonal skills
• The ability to work independently and collaboratively with shifting objectives, demonstrate good initiative, and attention to detail
• Scientific precision
• Strong customer-centricity

The following will be the primary duties of this position:

• Keep an eye on the clinical sites in France and the UK
• Communicate as necessary with Institutional Review Boards regarding Protocols, Informed Consent Forms, and other documentation
• Assist in the creation of document templates, pertinent Standard Operating Procedures (SOPs), and rules by serving as a supplementary contact between the organisation and the Institutional Review Board
• Make sure all clinical study source documents and/or forms are accurately and completely documented in accordance with the company's SOP, GCP, and any other applicable regulations
• Work closely with clinical staff and the Principal Investigator to ensure that clinical documents are produced to the standard required by Good Clinical Practice (GCP)
• Complete all tasks in accordance with SOPs, GCP, and all applicable regulations.
• Gather research materials

Get in touch with me ASAP to find out if this position would be a good fit for you!

Email: gjohnstone@barringtonjames.com

Phone Number: +44 1293 77 8 666