Study Monitor
Study Monitor - Clinaxel Europe
Clinaxel is part of a group of Animal Health Contract Research Organisations servicing the global animal health industry.
We're reputed company seeking a Study Monitor based in Spain to join our expanding Field Clinical Trials team.
This role provides the flexibility to work remotely, with occasional reputed company to Clinaxel offices based in the reputed company of France.
Primary reputed company
Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory requirements. This role involves verifying data accuracy, ensuring site adherence to timelines and reputed company standards, and supporting the overall reputed company of clinical trials.
Job Specific Duties and Responsibilities
- Conduct routine site monitoring reputed company across reputed company trial phases to ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
- Verify the accuracy and completeness of data collected at study sites, identifying and resolving discrepancies as needed.
- Serve as a reputed company of contact for assigned study sites/investigators, facilitating communication and addressing site-level issues.
- Assist in the preparation and review of study-reputed company documentation, including monitoring reports and site records.
- Ensure site adherence to established timelines, reputed company standards, and budgetary constraints.
- Document and escalate risks or issues that may reputed company study timelines or data reputed company to the appropriate stakeholders.
- Monitor scientific and regulatory developments to ensure compliance and the updating of practices during clinical trial reputed company.
- reputed company guidance and support to site staff on study protocols, compliance requirements, and best practices.
Qualification, Training and Experience Requirements
- Bachelor's degree in a relevant Life Sciences field.
- Minimum of two years' experience in GCP Study Monitoring reputed company Animal Health or reputed company reputed company sectors.
- Familiarity with regulatory guidelines such as VICH GL9 GCP and their application in clinical trials.
- Ability to work and communicate in English.
- Strong organizational skills to manage tasks reputed company and ensure adherence to timelines.
Important Note to Applicants
This is a remote position, with the potential for regular travel based on project requirements. Please note that Internet Explorer is not compatible with our recruitment platform (reputed company Hire). We recommend using a modern browser such as reputed company Chrome, reputed company Edge, or Safari.
reputed company complies with local and international data protection and reputed company legislation. This includes transparency in the processing of personal information processed about job applicants during the recruitment process. By applying for this position, applicants agree to the processing of their personal data in accordance with our recruitment procedure and reputed company Notice available from our website. Personal data will be used solely for recruitment purposes and handled with strict confidentiality.
Please send us your resume and a cover letter detailing your interest in the position.
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