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 Erol Onel, M.D. is an experienced physician with strong clinical and academic background coupled with industry experience (all phases: 1, 2, 3a, 3b, and 4 in both large and small pharmaceutical companies) and corporate/market focus, who can bring leadership across therapeutic areas, speed drugs and devices to market, and expand product life-cycles.
Erol Onel, M.D. Senior Associate Director, Clinical Operations (General Medicine: Female Sexual Dysfunction)
- Trial Clinical Monitor for 975 subject and 4000 subject Phase 3 trials
- Exceeded recruitment goals by 200 subjects in three months less than allotted
- Managed $13 Million and $42 Million projects ahead of time and under budget
- Primary role in guiding department when Director position vacant
- Facilitated inter-department and external communications
- Authored study protocols, NDAs, and clinical development plans
- Led team of 11 MDs, PhDs, and RNs in finding creative solutions to FDA & EMEA requests
- Authored, validated, and published new ratings scales and outcomes instruments
- Regular interaction with clinical trial investigators, industry experts and thought leaders
- Designed worldwide safety data reporting process, form, and database in 13 countries
- Reviewed SAE reports, reviewed and wrote patient narratives
- Potential for $9 Million increase in company revenue by decreasing time to market 90 days
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