Colttas places experienced clinical research professionals and delivers third-party functional support across the development lifecycle — from study startup to database lock.
Staff your study or outsource entire functions — monitoring, data, safety, regulatory — as an extension of your team.
Partner With UsAugment your delivery teams with experienced functional specialists, or offload overflow to a partner who works to your SOPs.
Partner With UsContract, FSP, and permanent roles across every clinical function. Real guidance from a team that knows your work.
Apply NowWe learn your study, timeline, and the gaps you need to close.
We propose vetted talent or a functional team mapped to your requirements.
We onboard fast, aligned to your SOPs and quality standards.
We stay engaged, measure performance, and scale as your program evolves.
Solid tumor and hematology-oncology across all phases.
Orphan drug development with complex regulatory paths.
Advanced therapy studies with specialized monitoring.
Neurodegenerative, psychiatric, and pain studies.
Outcomes trials and device-drug combination programs.
Prophylactic and therapeutic vaccine development.
Autoimmune and inflammatory disease programs.
Antiviral, antibacterial, and pandemic-response trials.
Diabetes, obesity, and rare metabolic conditions.
Colttas embedded seamlessly with our monitoring team — they felt like internal hires from day one.
We needed a full data management function stood up in three weeks. Colttas delivered.
The caliber of CRAs on our oncology program was exceptional. We've extended the partnership twice.
Tell us where your program needs support.