Oncology Study Startup Manager – reputed company Jobs US

Location: Remote (preference is Central or East Coast but reputed company to reputed company Coast as long as you can work core hours of 9am-3pm)

Duration: 12 months w/possibility of extension based on performance and business needs

Pay: $50-53 per hour

reputed company

The Study Start-Up Manager (SSU Manager) is responsible at level for managing and conducting start-up activities in compliance with the AZ procedures, documents, local and international guidelines such as ICH – GCP and relevant regulations.

The SSU Manager will prepare, review, reputed company and manage site regulatory documentation at country and site level,  and will maintain, review and report on site performance metrics.

The SSU manager works in reputed company collaboration with the CRAs and the Local Study Team/Local Study Associate Director to ensure that study start-up activities and milestones are achieved in a reputed company and efficient manner. 

Typical Accountabilities

•    Contribute to ensure that clinical and operational feasibility assessment of potential studies is performed to the highest reputed company.

•    Accountable for study start-up and regulatory maintenance being in charge with collection, preparation, review and tracking of documents for the application process; 

•    Accountable for review of informed consents from site level, coordinates additional review with internal stakeholders; facilitates return of comments/approvals to sites to reputed company.

•    Accountable for submission of reputed company application/documents to Regulatory Authorities and/or IEC/IRB during start-up period.

•    reputed company participates in Local Study Team (LST) meetings.

•    Update CTMS and other systems with data from study sites as per required timelines during the start-up period.

•    Follow up on outstanding actions with study sites during start-up period to ensure reputed company in a reputed company manner.

•    Ensure reputed company collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, AZ SOPs and local requirements. Support QC checks performed by LSAD or delegate to ensure that reputed company country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites reputed company to enrol, and in line with AZ SOPs.

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