Freelance Clinical Research Associate
hace 4 meses
**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 of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison 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 cultures 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 of clinical sites, maintenance of study files, conduct of pre-study initiation visits, regular visits and close out visits, assists on audit/inspection visits and assists in site and vendor contracting process, liaison 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 skill
**Benefits**:
- Working with experienced and very professional and supportive team
- Competitive remuneration
- Flexible working time
**Location**:
- Home-office
- CRA must be located on Seville, Huelva, Cadiz or Cordoba.
- Availability to travel (Seville)
Tipo de puesto: Autónomo
Duración del contrato: 6 meses
Horario:
- De lunes a viernes
- Flexibilidad horaria
Experiência:
- ensayos clínicos: 2 años (Obligatorio)
Idioma:
- Inglés (Obligatorio)
Disponibilidad para viajar:
- 50 % (Obligatorio)
Ubicación del trabajo: Teletrabajo híbrido en 41001 Sevilla
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