Job summary: As an experienced Clinical Research Associate, you will be expected to actively participate in and manage the recruitment of potential investigators. You will be responsible for monitoring clinical sites, maintaining study files, conducting pre-study and initiation visits, liaising with vendors, and other duties. You will function as the primary contact for sites regarding regulatory compliance and protocol questions and communicate with clinical sites on an ongoing basis to address and resolve issues.
We are searching for an experienced, ambitious, and energetic person, able to undertake challenges in the project, push forward development of the project, and function well in the project team. The desired person shall be open to cross-cultural communication and cooperation and shall be significantly independent in their performance.
Main Tasks of the Position: Responsible for recruitment of potential investigators. Responsible for monitoring clinical sites, maintaining study files, conducting pre-study initiation visits, regular visits, and close-out visits, assisting on audit/inspection visits, and assisting in site and vendor contracting processes, liaising with vendors, and other duties. Functions as the primary contact for sites regarding regulatory compliance and protocol questions and communicates with clinical sites on an ongoing basis to address and resolve issues. Required Qualifications, Experience, Competencies: Excellent knowledge of the clinical trial process and ICH/GCP and local requirements/guidelines. Excellent organizational and time management skills. Skills to handle multiple priorities and to work with deadlines and under pressure. Excellent written and oral communication skills. Fluent in written and verbal English and Spanish. Computer skills. Benefits: Working with an experienced and very professional and supportive team. Competitive remuneration. Flexible working time. Location: Home-office. CRA must be located in Seville, Huelva, Cadiz, or Cordoba. Availability to travel (Seville). Job Type: Autónomo
Contract Duration: 6 months
Schedule: Monday to Friday. Flexible hours. Experience: Clinical trials: 2 years (Required). Language: English (Required). Availability to travel: 50% (Required). Job Location: Hybrid telework in 41001 Sevilla.
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