: Bachelors Degree in Pharmaceutical or related field Min. 1 - 2 years of clinical trial experience in the pharmaceutical or CRO... industry. Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP...
The Clinical Research Associate (CRAII - SCRA), is primarily responsible for ensuring the rights and wellbeing of trial... personnel to ensure the efficient, expedited and smooth management of clinical trials. Foster internal and external customer...
. Experience using e-clinical systems [e.g., clinical trial management system (CTMS)]. For medical device positions, experience...Summary Of Responsibilities Site management responsibility for clinical studies according to Fortrea's Standard...
This team ensures Pfizer's Clinical Study Report (CSR) management meets global agency standards and manages regulatory... components and seek resolutions Seek approval from signatories on finalized CSRs and update clinical trial registry with CSR...
This team ensures Pfizer's Clinical Study Report (CSR) management meets global agency standards and manages regulatory... components and seek resolutions Seek approval from signatories on finalized CSRs and update clinical trial registry with CSR...
. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review..., and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment...
. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review..., and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment...
. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites... future of clinical development. We are currently seeking a Site Management Associate I to join our diverse and dynamic team...
. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites... future of clinical development We are currently seeking a Site Management Associate I to join our diverse and dynamic team...
Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage... practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent...
such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP):Assesses... documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention...