Linda Herbert

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clinical research cro clinical development early phase trials post market studies observational research real world evidence studies investigator initiated trials medical device clinical investigations nutraceutical studies medical affairs & medical writing regulatory trials startup data management pharmacovigilance quality assurance eclinical platform project control statistical analysis & consultancy staudy management & monitoring preclinical & drug development consultancy medical monitoring medical feasibility other services research services clinical trials study management regulatory compliance medical affairs safety vigilance biostatistics statistical analysis advanced therapies hematology oncology cns pediatrics medical devices infectious diseases rare diseases respiratory diseases cardiovascular diseases immunotherapy targeted therapies protocol development project management clinical data solutions edc clinical trial management multi-country trials observational studies phase i-iv studies medical writing sops risk management gdpr compliance iso certifications ich-gcp compliance clinical operations real-time data availability customized solutions drug management laboratory management third-party data handling ai in clinical trials electronic data capture clinical trial monitoring safety monitoring patient recruitment progress reporting contract research organization (cro) comprehensive clinical support drug development medical device vigilance clinical strategy development electronic data capture (edc) investigator initiated trials (iits) compassionate use programs project execution multi-country studies therapeutic areas innovation teamwork transparency ethical practices customer demographics market analysis real-world evidence pharmaceuticals biotechnology global presence quality consultancy cost-effective solutions flexibility adaptability health care health wellness & fitness hospital & health care productivity medical