The clinical research environment continues to rapidly evolve across global markets. You need qualified people with specialised expertise that includes the right therapeutic experience, a broad understanding of regulatory trending and tested clinical development processes and procedures. We find, engage and retain the right people to ensure your project moves quickly and efficiently through the phases of clinical trials. Actalent’s global access to talent, combined with our customised delivery models fill the gaps in your capabilities, enabling you to effectively execute on current research projects as well as take on additional work and impact the lives of more people.
As new technology in artificial intelligence emerges to support automation, virtual trials, mobile health, and wearables, you need a flexible, strategic partner who invests in the appropriate systems, software, and training that accelerate clinical trials. Expertise in applying technology also reduces errors and risk while improving reporting, with increased accuracy in monitoring, surveillance and advanced analytics. Combined with our engineering and laboratory capabilities, we can support your work from initial R&D through the final manufacturing of drugs and medical devices. Our people look forward to new challenges, and we provide the coaching, mentorship and growth that improves their delivery on your needs.
We specialise in:
- Drug safety and pharmacovigilance
- Clinical operations
- Biometrics and epidemiology
- Scientific research and development
- Pharma technology