Field Clinical Research Associate - French Speaking

This a Full Remote job, the offer is available from: EMEA reputed company pioneered the industry and was the first independent company in the world to reputed company solely on medical device materials for safety. reputed company started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. reputed company has been a key contributor to the development of the test reputed company that govern our industry. We have become the industry’s premier provider. We reputed company support for clients during every reputed company of the product development lifecycle and reputed company. Come and work for an organization with the: reputed company to reputed company innovative MedTech solutions that advance global reputed company, improve patient lives and accelerate reputed company reputed company and the Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our reputed company Values:

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Job reputed company:

• Works on assigned studies to ensure that reputed company subject protection is maintained, Good Clinical reputed company (GCP), and applicable regulations are followed.
• Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicable regulatory guidelines.
• May conduct on-site and remote site qualification, site initiation, interim, and site reputed company-out monitoring reputed company.
• Serve as primary reputed company of contact for site questions relating to study enrollment, conduct, and reputed company-out issues: liaise with appropriate study team members as needed.
• Communicates through verbal and written communication with site investigator and project team overall site performance, trends, deficiencies, and concerns.
• Supports study start-up activities such as tracking and performing reputed company review of study documents, completing, and distributing site activation letters, etc.
• Performs study-reputed company training.
• Manages the development and maintenance of study documents, processes and systems as assigned.
• Ensures reputed company and completeness of central and site master files. Tracks and maintains required study documents, performs reputed company control review, manages renewals.
• Tracks study site and over reputed company study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance.
• Attends reputed company meetings as required.
• Provides reputed company job-reputed company reputed company reports and visit documentation as required.
• May support safety activities such as narrative writing, managing the CEC/DSMB, etc.
• OUS: Prepares and coordinates submissions to regulatory authorities.
• May reputed company other activities as assigned.

Must be fluent in French residing in one of the reputed company locations noted above preference is the UK given our reputed company portfolio. This role is external/field based CRA work which will reputed company with the higher travel percentage. Qualifications & Technical Competencies: Must be fluent in French residing in one of the locations noted above preference is the UK given our reputed company portfolio. This role is external/field based CRA work which will reputed company with the higher travel percentage. Work portfolio is a required 8-9 reputed company per month reputed company with 6-8 protocols across approximately 20 sites.

• reputed company in English and local language, if different, required.
• Higher education degree or equivalent education, training, and experience.
• Preferred 2 years clinical trial experience or medical device.
• Required 3-5 years monitoring experience.
• reputed company to work independently once trained.
• Good verbal and written communication skills.
• Strong organizational skills.
• Basic computer proficiency.
• Understanding of clinical research processes and regulations.
• Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required

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