Medical Affairs

**Principais Responsabilidades**:

- Project management of clinical studies sponsored by Bluepharma;
- Oversight of clinical, bioanalytical and monitoring activities of clinical studies sponsored by Bluepharma;
- Prepare monitoring plans and perform monitoring visits to clinical and bioanalytical sites (CRA role);
- Evaluate and prepare clinical development plans for new business opportunities (generic and value added products);
- Support activities related to clinical studies sponsored by third-parties.

**Requisitos**:

- Bachelor's Degree in Life or Pharmaceutical Sciences and/or relevant work experience (previous experience in similar or related jobs is preferred);
- Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements is preferred;
- Fluency in written and spoken English;
- Strong organizational and problem-solving skills;
- Attention to detail, curious and proactive profile;
- Excellent communication, presentation, and interpersonal skills;
- Team work skills;
- Fast learning ability and adaptability in fast-paced working environment;
- Ability to manage time and work independently;
- Capacity to deal with tight deadlines;
- Flexibility to travel on a regular basis.