The development of new drugs and novel therapies is more important than ever. At the same time, the regulatory environment grows ever more complex – and compliance more expensive. To accelerate the process while staying on top of costs and reporting requirements, the biopharma industry requires a partner who can navigate this landscape with ease.
As staffing experts across the biopharma space, Randstad helps fill roles for multiple key functions, including clinical trial management, medical writing, biometrics, pharmacovigilance, and regulatory compliance. With these skill sets on your team, you are well-equipped to take a drug from the preclinical phase to full FDA approval – on time and with little or no cost overruns. We can also supply support professionals to augment your staff during any and all steps of the process. The help you need, when and where you need it.
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