Piedmont Healthcare

Sr. Clinical Trial Manager

US, Blue Bell (ICON) · Senior · Contract

No sponsorshipDetected 9 days ago

GCPAccessibilityNegotiationForecastingVendor ManagementClinical TrialsClinical ResearchResearchCommunicationCollaboration

About the role

Promptly communicates relevant status information and issues to appropriate stakeholders - Focuses on investigator engagement through timely follow up with sites.
May conduct accompanied site visits with SM, if delegated by Sponsor. - Ensure accurate finance reporting and trial delivered within budget by adhering to finance reporting deliverables and timelines.
This includes forecasting and proactive management of country/local trial budget.

We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
Serves as the primary point of communication for sites, facilitating internal client teaming to drive issue resolution.
Intimately understands site operational model and owns relationships with critical site stakeholders to provide a voice for the site to the client's teams.
Collaborates with central study team and local stakeholders as applicable for final selection of sites to participate in trial.
Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress.
Delivers competent vendor management at the country level to support the study and may submit requests for vendor services and support vendor selection.
Contributes to patient understanding of protocol and patient safety by preparing country specific informed consent in accordance with procedural document/templates.
This includes reviewing and managing site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations.
Keeps oneself inspection ready and knowledgeable for current work by complying with relevant training requirements and developing therapeutic knowledge enough for role and responsibilities.

This includes reviewing and approving site and local vendor invoices as required.
As required, manages the local study supply.
Ensures trial subject safety in that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented, as appropriate.

Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Visit our careers site to read more about the benefits ICON offers.

May conduct accompanied site visits with SM, if delegated by Sponsor. - Ensure accurate finance reporting and trial delivered within budget by adhering to finance reporting deliverables and timelines.

This listing is sourced directly from Piedmont Healthcare's careers page and normalized into a canonical job model.