Clinical Study Coordination

**DESCRIPTION**:
The Study Coordinator (SC) successfully supports the site's Principal Investigator (PI) in the development, monitoring, implementation management, and closeout of assigned protocols. The SC will support, facilitate and coordinate the daily clinical research study/studies activities and play as a critical role in the conduct of the study.

**FUNCTIONS**:
protocol, institutional policies, Good Clinical Practices (GCP) and the relevant regulatory requirements.

**SKILLS AND EXPERIENCE**:

- The SC must be a medical doctor with experience in clinical research.
- Familiarity with applicable international, US, and Indonesian regulations and guidelines pertaining to clinical research, including ICH- E6 Good Clinical Practice Guidelines
- Ability to coordinate complex systems for research quality control.
- Excellent organizational and time management skills.
- Ability to keep detailed and accurate records.
- Very strong interpersonal skills, flexibility and strong written and verbal fluency in Spanish and English.
- Strong written and verbal communication skills.
- Prior clinical research experience as a study coordinator, investigator, research nurse, clinical research associate, monitor or similar is strongly preferred.

Tipo de puesto: Tiempo completo, Por tiempo indeterminado

Salario: $25,000.00 - $28,000.00 al mes

Horario:

- Lunes a viernes
- Turno de 8 horas

Prestaciones:

- Opción a contrato indefinido
- Seguro de gastos médicos mayores
- Seguro de vida

Lugar de trabajo: Empleo presencial