Clinical Trial Experts
Contract Research Organization Services
RP-CRO staff and research sites are experts in conducting clinical trials
Research Professionals offers comprehensive CRO services for a wide range of pharmaceutical and medical device clinical studies. Having access to the region’s leading research study sites, an exceptional Principal Investigator (PI) network, Research Professionals has a proven track record of managing studies both large and small. With more than 150 experienced and dedicated staff, Research Professionals brings direct experience having successfully managed over 75 studies in more than 15 therapeutic areas.
We do all of this while maintaining the highest standards and meeting current regulations in order to deliver only high-quality clinical research studies to our global customer base. Based in Central and Eastern Europe (CEE), Research Professionals CRO applies its experience, knowledge, and technology to help clients to complete studies faster and more cost-effectively.
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Contract Research Organization (CRO) Services
We effectively support our customers through all phases of running clinical trials including:
- Clinical Study Feasibility Assessment
- Start-up Regulatory Requirements Evaluation
- Development of Study Related Documents
- Biostatistics and Protocol Design
- Vendor Selection & Management
- Site selection and qualification
- Site Budget and Contract Management
- Site initiation
- Clinical Trial Monitoring Activities
- Regulatory Management Services
- Vendor Management
- Subject Travel Expense Reimbursement Services
- Statistical analysis
- Medical writing
- Regulatory approval / registration
- Executive Search and Recruitment
- Human Resources (HR) Outsourcing
Research Professionals Member of ACROSS Global CRO Network
Research Professionals is a proud member of ACROSS Global, a strategic alliance of qualified clinical research organizations (CROs) that enable regional CROs to seamlessly provide expanded services in additional markets as required by the study. There are ACROSS Global member organizations located across 99 countries with access to more than 8,835 study sites, and the collective experience of greater than 212,000 patients recruited in 25+ therapeutic areas. With over 2,500 skilled employees, ACROSS Global members are fully dedicated to conducting cost-effective clinical studies to the highest global standards. A well-balanced combination of local knowledge, globally experienced professionals, and the latest technology allows Research Professionals in combination with the ACROSS Global CRO alliance to deliver faster, more cost-effective studies without sacrificing quality just about anywhere in the world.
As part of the ACROSS Global network, Research Professionals can offer full service clinical operations internationally.
- Selecting and managing the central laboratory
- Developing Clinical Study Reports (CSRs)
- Designing drug labels
- Developing, reviewing, and adapting Informed Consent Forms (ICFs)
- Organizing Investigator meetings
- Institutional Review Board (IRB) submissions (Research Ethics Boards – REBs)
- Translating and adapting legal documentation
- Monitoring Study plan development
- Obtaining local insurance
- Budgeting and planning the project
- Project status update report
- Developing and finalizing diaries
- Reviewing and finalizing questionnaires
- RA/CIRB Initial Submission and Protocol Amendment Submission
- Processing Serious Adverse Events (SAE) and Suspected Unexpected Serious Adverse Reactions (SUSAR)
- Site Management (site identification and selection, qualification visits, document collection, initiation visits, monitoring visits, close-out visits, payment processing)
- Sponsor SOP training
- Selecting and managing the study depot
- Preparing study materials
- Training study teams
- Vendor selection and management