Place expert clinical research professionals on your team, or outsource entire functions to us. Most partnerships use both — scaled to where your program needs support.
Contract, permanent, and Functional Service Provider (FSP) placement of experienced research professionals — pre-screened for therapeutic experience, system fluency, and GCP rigor, and matched to your protocol and timeline.
Site monitoring at every level of seniority, on-site or remote.
CTMs and CPMs to lead delivery, timelines, and cross-functional execution.
Data quality, oversight, and team leadership through to database lock.
Activation, submissions, and essential document management.
Coordination and site-level capacity to keep enrollment moving.
Safety professionals for case processing, reporting, and surveillance.
Statistical analysis and programming aligned to CDISC standards.
Physician oversight for medical and safety decision-making.
When you need capability rather than headcount, Colttas owns the work. We run functions end-to-end against your SOPs and quality standards — accountable for outcomes, not just hours.
Monitoring plan development, on-site and remote visit execution, source data verification, and timely issue identification and escalation.
Study timeline and milestone management, risk-based oversight, vendor coordination, and sponsor-grade reporting.
Site selection and feasibility, IRB/EC submissions, essential document collection, and regulatory intelligence.
CRF design, edit-check programming, ongoing data review, query management, and database lock.
SAE/SUSAR processing, CIOMS and MedWatch reporting, signal detection, and safety narrative writing.
CSRs, IBs, and protocols, plus IND/NDA/BLA submission support and supporting documentation.
GCP compliance, TMF review, CAPA management, and inspection preparation and support.
SAP development, SDTM/ADaM datasets, TLF production, and CDISC-compliant deliverables.
We represent experienced professionals across the industry — and we treat your career like the long-term investment it is, not a single placement.
Opportunities aligned to your experience, therapeutic focus, and the kind of work you want next.
Honest market insight and guidance on growth, rates, and the moves that advance your career.
Flexible contract, FSP, and permanent opportunities across sponsors, biotech, and CROs.
Preparation, protocol context, and feedback so you walk into every interview ready.
Whether we're placing talent or running a function, the path is structured, transparent, and built around your study.
We capture role scope, therapeutic context, systems, and timeline with your team.
We shortlist pre-vetted candidates and validate experience, references, and GCP currency.
You meet a focused slate; we coordinate scheduling and feedback end-to-end.
We manage offer, onboarding, and ongoing check-ins to keep the placement performing.
We map deliverables, dependencies, and quality expectations against your protocol.
We assign the right functional team and agree governance, timelines, and KPIs.
We deliver against SOPs with proactive risk management and regular reporting.
We measure performance, refine, and flex capacity as your program evolves.
From a single specialist to a fully outsourced function, we'll scope the right engagement for your program.