Pharmaceutical, biologic, and medical device development services: Clinical research trials management, monitoring, & auditing; Data management; Regulatory affairs, medical writing, & FDA submissions; QA/QC auditing and training.

global, contract research organization, cro, clinical, development, organization, clinical development organization, clinical trial, clinical trials, trial, trials, management, development trials, design, consulting, services, consulting services, allergy, respiratory, product development, product, development, cardiovascular, cns, oncology, therapeutic, protocol design, protocol, case report form, crf, patient recruitment, patient, feasibility, data, informed consent form, icfs, pharmacology, phase i, phase ii, phase iii, phase iv, phase i-iv, postmarketing surveillance, postmarketing, surveillance, biostatistics, biostatistical analysis reporting, biostatistical, analysis, reporting, pharmacokinetics, pharmacodynamics, regulatory consulting, regulatory, pharmaceutical, biotechnology, medical, device, principal investigator, investigator, investigators, investigational, new drug, drug, applications, ind, ndas, investigate, electronic data capture, edc, regulatory, fda, mca, ctx, submissions, approval, support services, clinical research associate, cras, cra, careers, clinical research, clinical, research, medical monitoring, monitoring, data safety, safety, monitoring boards, monitoring, dsmbs, dsmb, institutional review board, irbs, irb, data monitoring committee, dmcs, dmc, electronic regulatory submission, pivotal, first time in man, studies, gcp auditor, gcp, auditor

pra is one of the world's leading global clinical development organizations with more than 3,000 employees worldwide delivering reliable service, program-level therapeutic expertise, easy global access to knowledge and an involved senior management to our customers.