The Clinical Project Manager is responsible for project management expertise for clinical trials. Create and oversee project timelines and budgets, manage competing timelines and prioritize critical tasks. Contribute to the creation and review of essential trial documents such as protocols, informed consents, case report forms, clinical study materials and monitoring tools. Ensure appropriate versioning and translations of documents. Schedule and...
The Clinical Trial Manager is responsible for the day to day operation of a given clinical study. Responsibilities include. The development of clinical protocols, Investigator’s Brochures, information/consent forms, training material, case report forms, diary cards, clinical study reports and other clinical documents, as required by the project. Participation in writing clinical sections in regulatory documents (e.g., BLA or IND). Manage internal...
Roles and Responsibilities. Clinical Quality Assurance Auditor will be responsible for. Schedule, prepare, conducts and reports assigned audits of the Client’s projects and operational processes in accordance with approved procedures, schedules and formats. Audits include Investigative Sites, Clinical Vendors, Clinical Study Reports and Trial Master Files. Provide clear, accurate and concise advice on GCP and compliance related questions from Ope...
The Clinical Project Manager is responsible for project management expertise for clinical trials. Create and oversee project timelines and budgets, manage competing timelines and prioritize critical tasks. Contribute to the creation and review of essential trial documents such as protocols, informed consents, case report forms, clinical study materials and monitoring tools. Ensure appropriate versioning and translations of documents. Schedule and...
The Clinical Trial Manager is responsible for the day to day operation of a given clinical study. Responsibilities include. The development of clinical protocols, Investigator’s Brochures, information/consent forms, training material, case report forms, diary cards, clinical study reports and other clinical documents, as required by the project. Participation in writing clinical sections in regulatory documents (e.g., BLA or IND). Manage internal...
Roles and Responsibilities. Clinical Quality Assurance Auditor will be responsible for. Schedule, prepare, conducts and reports assigned audits of the Client’s projects and operational processes in accordance with approved procedures, schedules and formats. Audits include Investigative Sites, Clinical Vendors, Clinical Study Reports and Trial Master Files. Provide clear, accurate and concise advice on GCP and compliance related questions from Ope...
