Delivery focused
What are the benefits your Sponsors get in collaborating with us?
As your mid-sized, full-service CRO partner, in addition to getting highly experienced staff allocated to your project, Optimapharm offers agility, flexibility and low turnover to all its clients. Our fantastic reporting capabilities allow you to access your study real-time data whenever you need to; all our reports indicate actual vs. plan. To increase the quality of your data, we partner with the leaders of the market to offer you best-in-class but affordable technology.
85%+
Repeat business
90%
of clients would collaborate on future studies
88%
of clients would recommend us to others
We can demonstrate a track record for consistently delivering accelerated project start-ups, over-achieving patient recruitment targets and completing studies ahead of schedule.
Our collaborative and commercially minded approach, combined with our market-leading access to cost-effective and participant-rich locations in Europe and North America, mean you can have confidence in our ability to meet your budget requirements.
Our people, your greatest asset
The success of a clinical trial is fundamentally dependent upon the expertise, experience and commitment of your CRO team.
Our reputation for operational excellence is founded on the quality of our highly educated staff: 29% have a higher degree; 70% hold an M.Sc. and B.Sc in pharmacy or life sciences; and 16% of the team are qualified Medical Doctors.
On average, our Clinical Operations team have more than seven years research experience while the members of our Clinical Project Management department bring an average of more than 11 years of expertise.
All of this, combined with an industry-leading staff turnover rate of less than 15%, means that your Optimapharm team is likely to remain consistently robust and efficient throughout the duration of your study.
Our established global network facilitates quick and easy access to key opinion leaders and world-class therapeutic area expertise when it is necessary to expedite a clinical trial.
