**Education and Experience**:
- Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or
- Direct experience in safety/Pharmacovigilance (comparable to 2 years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Knowledge, Skills and Abilities**:
- Therapeutic expertise across one or more medical specialty or sub-specialties (one being Oncology or Hemato-Oncology)
- Excellent interpersonal skills, influencing and team building skills
- Understanding of guidelines (FDA, ICH, EMA and GCP)
- Working knowledge of biostatistics, data management, and clinical operations procedures
- Ability to act as a mentor/trainer to other staff within pharmacovigilance
- Strong, well supported decisio...