Clinical research monitor

- Coordination of phase III and IV clinical trials in different areas: Breast Cancer, Prostate Cancer, Bladder Cancer, Non-Hodgkin's Lymphoma, Head and Neck Cancer, Dementia, Atopic Dermatitis, Psoriatic arthritis, Nodular Prurigo;
- Maintain accurate source documents related to all research procedures and be responsible for accurate and timely
data collection, documentation, entry and reporting;
- Schedule and participate in monitoring and auditing activities;
- Experience in vendor management;
- Contract and budget negotiation;
-Management of biological samples;
- Participate in investigator meetings.

The Master Program in Clinical Research Management aims to train highly qualified human resources to enable clinical
research.
Medical research, particularly clinical research, is a key activity for the development of health innovation. By its nature
and ethical issues, it is highly legislated, requires complex infrastructures and different basic research and is usually
done in the accumulation of functions with clinical activity. The structures that support research teams in the planning
and implementation of clinical trials is fundamental to their effectiveness and also ensure the correct application of
Good Clinical Practices.

The bachelor’s degree in Biomedical Pharmacy (BBP) provides training of professionals able to work in the interface
between classical careers such as Medicine and Pharmacy, particularly regarding all aspects concerning
pharmaceutical design and development and clinical trials. The follow up of medicines lifetime covers a set of skills and
Competencies that are spread, and this explains the need for new professionals oriented to scientific and technical
innovation, but with a good knowledge of the regulatory component which underlies this activity.