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CurAccel is a next-generation research organization, pioneering the use of innovative business and technology practices to provide comprehensive clinical development services for pharmaceutical, biotech, and medical device companies engaged in clinical trials and programs.


A global service provider founded in 2012, CurAccel supports the clinical development of drugs, biologics, devices, and diagnostics in Discovery and Phase I through IV clinical trials, complying with worldwide regulatory requirements. Clients may choose full-service clinical development or functional services (as needed) in more than a dozen therapeutic specialties.

Clinical Operations and Project Management


A properly managed project is characterized by a strong leadership team, a dedicated manager, a set of resources to implement a plan, and clear set of well-defined expectations and deliverables.


CurAccel offers a full project management team for local or global Phase I through IV trials in any therapeutic indication with any treatment modality.


A Project Manager (PM) is assigned to manage and oversee timelines and budget and act as the primary liaison for the sponsor.  A Clinical Team Manager (CTM) is assigned to direct site management and act as the primary contact liaison for investigators and site staff.

Staffing Solutions


Access to the most appropriate talent can mean the difference between success and failure. At CurAccel, we provide top talent to pharmaceutical, biotechnology, medical device, and contract research organizations.


Our network and database of professional talent have expertise in the following functional areas:

  • Monitoring / Site Management – In more than 12 different therapeutic areas

  • Data Management

  • Regulatory Affairs

  • Drug Safety

  • Study Management

  • Clinical Programming

  • Biostatistics

  • Medical Monitoring

CurAccel’s ability to act as a pivotal staffing player in the clinical research industry comes from our ability to locate, qualify, place and retain the perfect candidate for your clinical research projects.


Partnering with CurAccel allows your organization to receive resource support at any point during your clinical trial. We help you achieve optimal value through improved quality of personnel, increased efficiencies and overall program compliance.

Site Management Operations


We understand that choosing the “right” Investigative Site with access to the “right” patient population requires skill and experience. 


CurAccel has that skill and experience. We create teams of people who have practical, proven experience in implementing clinical trials and recruiting subjects.


  • Country and Site Feasibility

  • Site Identification and Qualification

  • Subject Recruitment

  • Site Monitoring

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