and filing processes across program and study functional areas (e.g. Clinical, Clinical Development and Sciences, Data Management... and maintenance of essential clinical trial and other designated documents, including the set up and maintenance of the electronic...
vendors (e.g., Clario, Signiant Health, Medidata, Clinical Ink) and a solid understanding of eCOA technical specifications..., and escalations, are essential. The candidate must also excel in collaboration and communication, guiding global clinical trial...
(from protocol development to Clinical Study Report) are delivered on time, within budget, and with high quality, in adherence...Industry: Lifesciences Industry: Pharma, Medtech, Digital Health Employment Type: Full-time Job Functions: Clinical...
, and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...Responsibilities: Provide leadership, strategic planning, direction and implementation of clinical systems for data...
to data management teams and stakeholders Act as Data Management Study Lead for multiple clinical trials Manage vendor...Responsibilities: Lead clinical data management activities for pivotal trials, ensuring data quality and integrity...
skills. Ability to travel to various clinical sites as required by the study protocol. Strong organizational skills..., and clients. Here at RDI, you own all of it. You’ll manage diagnostic clinical studies end to end — qualifying sites, designing...
. Position Specifics This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up..., and monitoring visit reports, while driving risk-based mitigation plans to proactively address study challenges. The position...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports...
in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...Responsibilities: Provide leadership, strategic planning, direction and implementation of clinical systems for data...