Lance White Email & Phone Number

Homestead, FL, US

Morrisville, NC, US

Reading, Massachusetts, US

• Duties include but are not limited to: The Sr. Clinical Trial Manager (Sr. CTM) provides clinical trial oversight to the assigned clinical(s), which may be complex or high priority, and ensures deliverables are met in.
• Development and tracking of Key Performance Indicators (KPIs) for clinical team members.
• Assist in the development of and programing of Clinical Trial Management System as related to key clinical repository. Test CTMS system before going live.
• Development of patient Informed Consent Forms, Study Protocols, Clinical Monitoring, Study Management and Safety Plans.
• Work with and manage study vendors post award through study closeout to ensure all deliverables are met.
• Responsible for the review of MVRs from the CRAs to ensure sufficient monitoring oversight is completed.

Morrisville, North Carolina, US

• Duties include but are not limited to:
• Point of contact to client study teams working with internal and external stakeholders Delivering project objectives on time and on budget
• Executing clinical trials end-to-end to ensure effective and timely internal and external communication of study progress, issues, and plans for resolution.\
• Develop Project Management and overall study plans. Review and approve ICFS, Protocols etc.
• Efficient resourcing and financial management of studies under his/her supervision. In this capacity, the Study Leader will have line management responsibilities ensuring that direct reports will have the appropriate.
• Lead weekly CTT and other cross-functional meetings.

Dublin, IE

• Line- managed and ensured collaboration within a team of Directors and Project Managers in the planning, execution and governance of projects/portfolios.
• Manage the resources to ensure that established cost, time, and quality goals are met
• Managed development; provide direction and support, and mentor PMs/PDs and/or their managers as needed
• Provided technical support and guidance (including scope definition, risk identification and mitigation, resource planning, goals and deliverables) to assigned PM staff.
• Planned capacity across new/existing PM/PD resources and secure needed resources whilst optimizing staff utilization/recovery.
• Keeps Global VP, PM, business sponsors, business-unit leadership and all stake-holders regularly informed of project/program progress, risks and issues through periodic reporting

Tokyo, JP, JP

Responsible for the planning, implementation, execution, and management of more than one clinical research studies.  Manages clinical outsourcing to CROs and other vendors such as IVRS, IRBs, Laboratories etc.  May author review and approve various study related documents and plans.  Evaluates issues, interpret data, and suggest and implements solutions.

Durham, North Carolina, US

Was responsible for the coordination functional groups and activities across all geographies, providing leadership and guidance to project team members  Liaise with project leadership and sponsor to ensure all deliverable's were met  Evaluate and identify resourcing needs and continuously monitor over life cycle of project  Monitor study timelines.

Fort Washington, PA, US

• Provided line management oversight for the Project Manager (PM) and Project Assistant (PA):
• Tracked current PA utilization to gauge adequate resources and request additional staff from management when necessary
• Assisted in the interviewing and hiring process of Project Manager and Project Assistant candidates as required for research projects according to Sponsor needs
• Provided oversight for direct reports including (1) approving and tracking of PTO requests, ensuring adhesion to the current RPS policy for PTO submission, (2) approving timesheets ensuring that adhesion to the current.
• Mentor new Project Managers in accordance to the Project Management Mentorship Program
• Evaluate and address employee performance through Sponsor feedback

Fort Washington, PA, US

• Managed multiple full scope projects from planning phase to analysis phase for delivery to client.
• Mentored Associate Project Managers
• Coordinated project organization, implementation and management activities between all functional areas and the client serves as primary contact for all projects related issues.
• Prepared the project plan and timelines and monitors against project progress; ensures project activity compliance with plan.
• Provided a leadership role in managing multiple Phase I through Phase IV clinical research trials across all functional areas. This position oversees and coordinates the operational aspects of ongoing projects to.
• Provided administrative oversight for direct reports including (1) approving ad tracking of PTO requests, ensuring adhesion to the current RPS policy for PTO submission, (2) approving timesheets & expenses ensuring.

Fort Washington, PA, US

• Provided a leadership role in managing multiple Phase I through Phase IV clinical research trials across all functional areas. This position oversees and coordinated the operational aspects of ongoing projects to.
• Coordinated project organization, implementation and management activities between all functional areas and the client. Serves as primary client contact for all project related issues.
• Assessed resource needs with functional area managers and establishes appropriate project team. Monitors ongoing resource needs to project.

• In a matrix environment, managed, lead and motivate the assigned cross functional project team, facilitating the team’s ability to fulfill their responsibilities in accordance with project contracts, contract.
• Developed and maintained relationship with the client’s study management team(s).
• Determined appropriate revenue forecasting and revenue recognition based on project plan, budget and contract deliverables.
• Tracked budget and scope changes, obtaining necessary client approvals for change in scope of work. Initiate and follow up on change order/contract amendment activities.
• Review, approve and follow-up on project invoices.
• Managed project resource needs and utilization according to project contract and contract amendments.

• Identified of potential investigational sites
• Monitored investigational clinical trials Phase II-IV in various therapeutic areas
• Coordinates and performs comprehensive site management
• Conducted of pre-study, initiation, interim and close out monitoring visits
• Produced comprehensive visit reports and status reports
• Resolved data issues and audit issues

• Identified of potential investigational sites
• Monitored investigational clinical trials Phase II-IV in various therapeutic areas
• Coordinates and performs comprehensive site management
• Conducted of pre-study, initiation, interim and close out monitoring visits
• Produced comprehensive visit reports and status reports
• Resolved data issues and audit issues

Durham, North Carolina, US

US