Candidates must have 3-5+ years of experience working in a pharmaceutical, biotechnology company or CRO including experience in on-site/field monitoring, study management and preferably 2 or more years in oncology.
Industry experience is required, as is oncology experience and early development, Phases I-II clinical trials.
Good understanding of Clinical Study Monitoring and Study Site management including clinical study processes, knowledge of ICH, GCP Guidelines and Regulatory Requirements.
Excellent verbal and written communication skills and ability to lead.
Able to travel approximately 25% of the time.
Candidate Must Have:
Field monitoring experience
Experience in pharmaceutical, biotechnology company or CRO