Job Purpose The Medical Director will be responsible for growing and leading a therapeutic portfolio through their medical and clinical development expertise and by providing medical and safety monitoring of awarded…
What You’ll Do: Therapeutic Strategy Leadership Serve as a champion for staying abreast of trends and development of treatments in assigned therapeutic areas (approaches to care, impact of regulations, patient…
About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill…
** Please submit your application and CV in English ** What You'll Do: Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead. Set goals, and…
What You'll Do: As the lead Biostatistician on the studies assigned, perform the following tasks: Act as primary statistical contact for internal and external project team members. Communicate and work with…
What You'll Do Review scope of project and resourcing related to Clinical Monitoring with Clinical Project Management Plan, schedule, and implement the clinical monitoring aspects of projects Define and implement…
What You'll Do: Initiate site contact and follow-up as necessary to turn study confidentiality agreements (CDA) and study clinical trial agreement (CTA) drafts Administer contract language to ensure it remains…
What You'll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables…
About the job Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge…
Senior Clinical Project Manager overseeing global clinical trials (Phase I-IV) for a CRO, managing timelines, budgets, client communication, and regulatory compliance (ICH-GCP).
This position is responsible for selling CTI clinical trial and regulatory and scientific affairs consulting services, including Phase I-III clinical trials and regulatory consulting services spanning pre-IND to NDA…
** Please submit your application in English ** What You'll Do: Initiate site contact and follow-up as necessary to turn study confidentiality agreements (CDA) and study clinical trial agreement (CTA) drafts…
** Please submit your application in English ** What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Assist/Advise project teams on all regulatory requirements for clinical studies…
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