Clinical Research Assistant

- Provide clinical support for projects according to Standard Operating Procedures, ICH Guidelines and GCP
- Act as contact for project team and study sites
- Assist with the management of study supplies and organize shipments
- Create, update, track, and maintain study-specific trial management files, tools, and systems
- Ensure compliance with SOPs, FDA, ICH, and GCP regulations for clinical conduct in all
aspects of daily work
- Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.

- Previous Experience in a corporate environment;
- Experience within clinical research preferred;
- Degree educated (Life Science);
- Fluency in local and English language;
- Understanding of the clinical trial process;
- Good oral and written communication skills;
- Ability to set priorities and handle multiple tasks simultaneously.

Key words: CRAss, CTA, CPA, assistant, clinical coordinator, In-House CRA, clinical research assistant, clinical studies, clinical research, CRO, pharmaceuticals, clinical project administrator, clinical trial assistant, clinical trials, Estonia, Tallin. THERE IS NO BETTER TIME TO JOIN US! Education/Qualifications * Experience * EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us. Application link