Allison Andersen Email & Phone Number

Boston, Massachusetts, Us

Abbott Park, Illinois, Us

Oversee DM activities from study startup through database lock. Responsible for conducting all aspects of clinical trials, including but not limited to: documentation, training, statistics, compliance, monitoring, and reporting.

Mansfield, Ma, Us

Independently led and drove Professional Services projects throughout the project lifecycle by consistently using PMI-compliant standards, and best practices.Successfully managed multiple clinical trial data management projects simultaneously, ensuring that proper documentation was developed and maintained, project risks were mitigated with a collaborative team approach, and client satisfaction remained at the forefront of all efforts.Collaborated with internal and external subject matter experts to plan, implement and support clinical trials for our clients.Improved PMO processes by contributing to PMO process documentation.Participated in SOP review to improve and enhance Data Management processes.

Morrisville, North Carolina, Us

Acts as the Functional Lead for Data Management full service contracts and as Project Lead for stand alone contracts.Plans, manages, and requests resources as required for assigned studies.Manages changes of scope, budget, revenue recognition, and participation inmonthly internal project reviews.Participates in, and presents at internal, customer, third-party, and investigator meetings.Trains and mentors data management staff.

Raleigh, North Carolina, Us

Acts as the Functional Lead for Data Management full service contracts and as Project Lead for stand alone contracts.Plans, manages, and requests resources as required for assigned studies.Manages changes of scope, budget, revenue recognition, and participation in monthly internal project reviews.Participates in, and presents at internal, customer, third-party, and investigator meetings.Trains and mentors data management staff.

Southborough, Massachusetts, Us

Serves as the Lead CDM contact with Sponsors on project teams.Creates and maintains essential CDM documents for assigned projects.Occasionally serves in a Project Management capacity on projects.Approves the building, testing, and validation of clinical databases.Creation of SOPs and data management processes.Ensures the Data Management team is up to date in training of relevant SOPs and receives proper training when needed.Provides training to clients as well as internal resources.Enhances and promotes internal Data Management consistency and communications.

Raleigh, North Carolina, Us

Serves as the primary INC Research CDM contact with Sponsors and represents CDM on project teams.Team Leader for multiple project teams.Responsible for project timelines, deliverables, reporting, and overall quality.Responsible for the creation and maintenance of essential CDM documents for assigned projects.Approves the building, testing, and validation of clinical databases.Coordinates the receipt and processing of information for projects (e.g., coding dictionaries) as well as electronic data received from specialty groups (e.g., lab data, e-diary data) utilized on projects.Occasional function as Biometrics Project Leader responsible for CDM, Programming, and Statistical services.Training of new associates in systems operation and discrepancy management.

Serves as the primary INC Research CDM contact with Sponsors and represents CDM on project teams.Team Leader for multiple project teams.Responsible for project timelines, deliverables, reporting, and overall quality.Responsible for the creation and maintenance of essential CDM documents for assigned projects.Approves the building, testing, and validation of clinical databases.Coordinates the receipt and processing of information for projects (e.g., coding dictionaries) as well as electronic data received from specialty groups (e.g., lab data, e-diary data) utilized on projects.Occasional function as Biometrics Project Leader responsible for CDM, Programming, and Statistical services.Training of new associates in systems operation and discrepancy management.

Reviewed and processed clinical trial data to ensure the accuracy and consistency of clinical databases for Phase II and Phase III studies.Facilitated audits adhering to the audit plan.Effectively trained new associates in systems training and discrepancy management.Participated in the training of Clinical Data Associates.Expected to lead teams of multiple CDAs and exhibit leadership skills.

Reviewed and processed clinical trial data to ensure the accuracy and consistency of clinical databases.Performed the following data related activities: CRF tracking, reviewing, validation, updating, SAE reconciliation, lab data reconciliation, and safety coding.Provided accurate, timely, and consistent clinical data to both sponsors and other internal departments to support the needs of Kendle.Participated in the training of Clinical Data Associates.

Reviewed and processed clinical trial data to ensure the accuracy and consistency of clinical databases for Phase II and Phase III studies.Facilitated audits adhering to the audit plan.Consistently addressed issues in Procedure Validation.Effectively trained new associates in systems training and discrepancy management.

New York, New York, Us

Proficiently entered data from Veterinary Medicine studies into AIMS database.Verified and audited data by comparing listings to original source documents.Identified data problem areas, conducted filing, and updated data for long-term study.