Jane Belanger Email & Phone Number

Hamilton, Ontario, Canada

Responsible for the end-to-end coordination of cross functional data collection and cleaning activities to ensure clinical study data deliverables are fit for purpose and align with the executed contract and sponsor expectations and timelines.Functional Lead for Clinical Data Science, ensuring required data elements and quality oversight steps are identified to support defined study analysis. Central steward of clinical data quality, monitoring risks through the holistic review of clinical and operational data, using high level knowledge of the protocol. Plan, manage, and request Clinical Data Science resources for assigned projects. Maintain budget oversight and identify out of scope activities for Clinical Data Sciences. Participate in, and present at Sponsor meetings on behalf of clinical data science responsibilities.

Hamilton, Ontario, Canada

As a senior research coordinator in data management I am primarily responsible for overseeing the day to day activities related to data management, safety, event adjudication, and protocol deviations management, and supervising data management and safety staff. My key responsibilities include:• Study plan oversight: execute, follow, and maintain the Data Management Plan (DMP) Adverse Event Report Plan (AERP) and Event Adjudication Plan (EAP)• Project planning, considering what the main tasks/projects for data management will be and how staff will be allocated. Identifying staffing needs and raising project and staffing issues for discussion with the Program Manager.• Provide leadership, coaching, training and mentorship to study team members; manage the performance and workload for study team members • Represent the research study team at program and other organizational meetings• Study database development: determining which CRFs are needed or when revisions are required, ensuring the review, approval, testing, and implementation process is followed according to study plans and PHRI SOPs; and working with all appropriate parties to implement new and revised forms and edit check programs in the study database.• Study database oversight: ongoing management of data collection, quality control, edit check programs, reports (identification, development and validation), processes and associated documentation

Hamilton, Ontario, Canada

As a research coordinator in data management I was primarily responsible for overseeing the day to day activities related to data management, event adjudication, and protocol deviations management, and for supervising data management staff.

Hamilton, Ontario

As a research coordinator in data management I was responsible for the oversight, collection, entry, verification, management, tracking, and reporting of data and other documents related to study management. I create data collection forms using FrameMaker, error checking methods and related programs for efficient collection, analysis and reporting. I troubleshoot problems in iDataFax. I prepare required study documentation/updates and other required tools for the project. I liaise with study centre personnel, study committee members and other related study personnel. I ensure relevant clinical and research methodology is applied, and proper handling of all clinical research material is used. I train and supervise data management assistants and research assistants and other study staff in the processing of study data.

Hamilton Ontario

As a research coordinator I assist the principal investigator in conducting a number of clinical trials for the treatment/prevention of Clostridium difficile infection using good clinical practice (GCP). I am involved with subject recruitment, patient care, and adverse event reporting. I prepare documents for review by the Research Ethics Board (REB), including research study applications, amendments, writing protocols, and informed consent documents. I prepare case report forms (CRF), and enter data into electronic case report forms for Sponsor studies.

Hamilton, Ontario

Involved in protocol development for randomized controlled trials primarily focussed on Clostridium difficile infection. Collected and extracted data. Created and maintained databases, and conducted systematic reviews.

Guelph, Ontario

Processed cash, check, debit and credit payments for merchandise. Balanced cash drawer and receipts. Trained new cashiers. Maintained a clean and tidy workspace.

Mississauga, Ontario

Efficiently assisted in development and refinement of modern composite, fiberreinforced, microsilica materials. Successfully and independently handled several assigned projects simultaneously.

Guelph

Processed cash, check, debit and credit payments for merchandise. Balanced cash drawer and receipts. Trained new cashiers. Maintained a clean and tidy workspace.

Guelph, Ontario

Independently issued worksheets and process orders. Proficiently reviewed, updated and implemented test procedures, worksheets and standard operating procedures.

Mississauga Ontario

Efficiently assisted in development and refinement of modern composite, fiberreinforced, microsilica materials. Successfully and independently handled several assigned projects simultaneously.

Self-Employed

Successfully educated students ages 4 – 13 in piano rudiments. Independently designed and organized lessons. Enthusiastically inspired students to achieve their goals

Cambridge, Ontario

Accurately and efficiently balanced tills, performed returns, exchanges, and change runs. Joyfully and artistically painted children’s faces.

Hamilton Ontario

Independently and precisely analyzed prephosphate coating weight ongalvanneal steal by inductive coupled plasma and xray methods. Competently assisted in quality control analysis. Reliably assisted in sample collection.

Msc, Applied Statistics

Hbsc, Chemistry Co-Op, Minor Math Science

Education record