Lorrianne Lewis Email & Phone Number

Parsippany, Nj

Manage the day to day activities of invoice reconciliation for frozen and dry accounts. Works collaboratively with the warehouses and cost manager to resolve price and receiving discrepancies. Responsible for timely submission of all invoices to AP. • Manage invoices for multiple accounts for frozen foods. • Ensure timeliness when processing, preparing, and approving invoices to be submitted for payment for accounts payable.• Process the manual inventory receipts into… Show more Manage the day to day activities of invoice reconciliation for frozen and dry accounts. Works collaboratively with the warehouses and cost manager to resolve price and receiving discrepancies. Responsible for timely submission of all invoices to AP. • Manage invoices for multiple accounts for frozen foods. • Ensure timeliness when processing, preparing, and approving invoices to be submitted for payment for accounts payable.• Process the manual inventory receipts into JDE.• Lead and conduct weekly meetings to review invoice reconciliation and inventory during the frozen pack season.• Review statement of accounts and reconciling outstanding invoices for payment.• Maintain invoice status reports for invoices for error resolution and to track monthly dollar amounts per vendor.• Train and mentor new Invoice Reconciliation Specialists.• Works with minimal supervision Show less

Berkeley Heights, Nj

Performed day to day functions as it pertains to data collection of clinical trial data into CTMS. Responsibilities may include, but are not limited to: collection of clinical documentation, data entry into Clinical Trial Management Systems, and ensuring accuracy of confidential data.• Follow established data collection rules and guidelines for data capture to sustain the quality of the data in the Clinical System • Establish relationship with respective study teams to ensure proper… Show more Performed day to day functions as it pertains to data collection of clinical trial data into CTMS. Responsibilities may include, but are not limited to: collection of clinical documentation, data entry into Clinical Trial Management Systems, and ensuring accuracy of confidential data.• Follow established data collection rules and guidelines for data capture to sustain the quality of the data in the Clinical System • Establish relationship with respective study teams to ensure proper interpretation of data entry into key clinical systems.• Read source documentations such as meeting minutes, protocols, vendor reports and enter data in specific data fields.• Perform data analysis and run quality control checks within Clinical System to ensure compliance to data capture procedures; interface with functional areas on quality issues through to resolution.• Ensures consistency and accuracy of information and reporting through periodic checks and identifies issues; resolves issues through data collection and reporting improvement efforts • Participation on clinical teams to obtain and share essential information for data entry and analysis; ensure validity of data across multiple stand-alone systems • Have knowledge and understanding of other relevant study/country/site/subject data and Clinical Study Management Systems Show less

Parsippany, Nj

• Manage invoices for multiple accounts for dry foods. • Ensure timeliness when processing, preparing, and approving invoices to be submitted for payment for accounts payable.• Process the manual inventory receipts into Inventory Management System.• Review statement of accounts and reconciling outstanding invoices for payment.• Maintain invoice status reports for invoices for error resolution and to track monthly dollar amounts per vendor.

Parsippany, Nj

• Tracked & Reviewed Pcard Invoices in the Medco GSP Workflow Console• Accessed & Update documents in MS SharePoint• Tracked, Updated & Reviewed HCP/AP Transactions in AggSpend• Tracked & Reviewed HCP and Corporate Expense Reports• Matched & Researched doctors, nurses & other healthcare providers in the MedPro database• Extensive research on the Internet to confirm & match HCP information• Performed a breakdown of HCP and corporate invoice transactions within Excel

Bound Brook, Nj

Responsible for performing the data management activities to ensure study and database was properly cleaned for submission. • Performed clinical data entry of Case Report Forms into Clinplus• QC of database listings against case report forms and updating of data in Clinplus database• Reconciliation and verification of clinical data • Assisted with user acceptance testing

Performed daily functions of the Clinical Data Associate role as it pertains to data entry, reconciliation, review, verification, and updating of clinical and regulatory documentations.• Supported Oncology studies from Phase I – Phase IV.• Submitted protocol revisions as it pertained to the data management plan.• Performed all activities to ensure data management deliverable meet/exceed project/study team expectations regarding quality, time and cost.• Performed all… Show more Performed daily functions of the Clinical Data Associate role as it pertains to data entry, reconciliation, review, verification, and updating of clinical and regulatory documentations.• Supported Oncology studies from Phase I – Phase IV.• Submitted protocol revisions as it pertained to the data management plan.• Performed all activities to ensure data management deliverable meet/exceed project/study team expectations regarding quality, time and cost.• Performed all activities to ensure Data Management documentations were filed appropriately in Trial Master File.• Trained fellow consultants on Data Management Activities. • Routinely interface with cross-functional team members• Participate in regular team meeting and provided input when necessary• Problem solving database issues until resolved Show less

Performed and assisted in data reconciliation, review, verification, and updating of clinical and regulatory documentations. Participated in the setup and merger of clinical data into a new database.• Performed clinical data entry from Case Report Form into ClinTrial, ensuring legibility, completeness, and accuracy of data • Maintained internal… Show more Performed and assisted in data reconciliation, review, verification, and updating of clinical and regulatory documentations. Participated in the setup and merger of clinical data into a new database.• Performed clinical data entry from Case Report Form into ClinTrial, ensuring legibility, completeness, and accuracy of data • Maintained internal record keeping systems within CDM• Performed QC data, provide status and activity reports as required• Reviewed and updated SOPs• Assisted users with requests for clinical documentations• Updated and archived essential data points in Excel • Supported Oncology studies from Phase I – Phase IV.• Performed all activities to ensure data management deliverable meet/exceed project/study team expectations regarding quality, time and cost.• Performed all activities to ensure Data Management documentations were filed appropriately in Trial Master File.• Trained fellow consultants on Data Management Activities. • Routinely interface with cross-functional team members• Participate in regular team meeting and provided input when necessary• Trouble shoot database issues until resolved Show less

Day to day functions as a Clinical Data Associate include data entry into EDC, reviewing data, posted data queries and resolved queries and discrepancies.• Performed Quality Control (QC) of database listings of clinical and non-clinical documentations, including SAEs and lab data. Liaised with clients as management and oversight of outsourced clinical trial. • Reviewed and updated SOPs• Applied knowledge across studies to make project decisions and show project… Show more Day to day functions as a Clinical Data Associate include data entry into EDC, reviewing data, posted data queries and resolved queries and discrepancies.• Performed Quality Control (QC) of database listings of clinical and non-clinical documentations, including SAEs and lab data. Liaised with clients as management and oversight of outsourced clinical trial. • Reviewed and updated SOPs• Applied knowledge across studies to make project decisions and show project leadership• Performed data reconciliation, review, and processed updates to clinical data.• Validated database information for clinical drug.• Processed edit checks• Generates and tracks data clarification forms • Lead and managed supported Oncology studies from Phase I – Phase IV.• Performed all activities to ensure data management deliverable meet/exceed project/study team expectations regarding quality, time and cost.• Performed all activities to ensure Data Management documentations were filed appropriately in Trial Master File.• Trained fellow consultants on Data Management Activities. • Routinely interface with cross-functional team members Show less

• Participated in reconciliation and entry of data during data merger after acquisition.• QC of CRFs

Clinical Data Coordinator• Data entry• Data reconciliation• QC• Data Validation• Data cleaning• Leadership of multiple oncology studies• Delegated assignments to Junior processors• Attend and participate in multi-departmental meetings regarding clinical trialsClinical Operations Specialist• Site recruitment• Site initiation• Site enrollment• Participate in investigative meetings as necessary

Bsba, Business Administration/Information Systems

Certificate In Advanced Clinical Research, Advanced Clinical Research

The Advanced Clinical Research Associate Certificate program is to develop and train students to understand and navigate an array.

Certificate, Ms Ofiice Specialist/Medical Billing And Coding

NCICS Certified Medical Biller and Coder

Aa, Business Administration