Clinical Study Service Experts

Contract Research Organization (CRO) Services

Research Professionals CRO staff are experts in conducting clinical studies
Research Professionals offers comprehensive CRO services for a wide range of pharmaceutical and medical device clinical studies. Having access to the region’s leading clinical study sites and an exceptional network of Principal Investigators (PIs), Research Professionals has a proven track record of managing clinical studies both large and small. With more than 150 experienced and dedicated CRO staff, Research Professionals brings direct clinical study management experience to every sponsor clinical study, having successfully overseen more than 75 of them, covering in excess of 15 different therapeutic areas.
Research Professionals always maintains the highest quality and clinical standards while meeting the most stringent regulations in order to deliver complete and compliant clinical studies for global customers. Based in Hungary, Research Professionals CRO supports clinical study operations in EU member countries that include Poland, Czechia, Romania, and Bulgaria, providing an integrated CRO network across much of Central and Eastern Europe (CEE), that serves the world. The result is expert clinical studies management that helps customers to complete their important studies faster and more cost-effectively with uncompromising quality.

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Contract Research Organization (CRO) Services
We effectively support our customers throughout all phases of clinical studies including:

Clinical Study Start Up Phase

The start-up phase of any clinical study is critical to maintaining target timelines. Research Professionals CRO starts with a thorough feasibility assessment and performs all the initiation steps required to begin the clinical study fast and on budget.

  • Clinical study feasibility assessment
  • Start-up regulatory requirements evaluation
  • Development of clinical study related documents
  • Biostatistics and protocol design
  • Vendor selection & management
  • Site selection and qualification
  • Site budget and contract management
  • Site initiation

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Five Research Professionals CRO clinical team members sitting around large wood table reviewing start-up study documents.
Clinical Study Conduct Phase

Once the study is approved to begin, Research Professionals CRO oversees the clinical study management role, compiles data, manages vendors and takes care of the ongoing critical details so you don’t have to. RP-CRO study conduct services include:

  • Clinical study monitoring activities
  • Regulatory management services
  • Vendor management
  • Subject travel expense reimbursement services

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Three Research Professionals CRO medical staff in blue scrubs review subject medical results in clinical setting.
Post-Clinical Study Activities

After the clinical study has been completed, Research Professionals completes the data compilation and analysis which it then formats in submission ready formats.

  • Statistical analysis
  • Medical writing
  • Regulatory approval / registration

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Five regulatory professionals meeting in board room to review clinical study data and submissions for regulatory review.
Human Resource Services

Research Professional’s CRO focused recruitment agency helps you to find the best and most experienced clinical research staff available. We specialize on clinical study management recruiting because we are experts in the field.

  • Executive Search and Recruitment
  • Human Resources (HR) Outsourcing

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Four people in business attire seated around wooden table shaking hands for clinical research recruitment (HR) meeting.

Research Professionals Member of ACROSS Global CRO Network
Research Professionals is a proud member of ACROSS Global, a strategic alliance of qualified Contract Research Organizations (CROs) that enable regional CROs to seamlessly provide expanded clinical study services in additional markets as required. The ACROSS Global CRO Network has allowed Research Professionals to manage international studies with clinical sites beyond our extensive CEE network of sites. There are ACROSS Global member organizations located across 99 countries offering 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.

Research Professionals offers complete CRO services from start-up through study conduct to post clinical study services. With years of experience and a strong track record for high levels of quality and regulatory compliance, Research Professionals CRO manages clinical studies for drug products and medical devices to customer budget and timeline. Contact RP-CRO to accelerate and derisk your next clinical study program.

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