Alexander Macpherson Email & Phone Number

Orillia, On, Ca

Toronto, Ontario, Canada

Remote

Oversees all the Data Management aspects on a clinical study under supervisionDevelops the Database setup/Data Entry Screens/Data Validation tools under supervisionContributes to maintain data validation on a clinical study under supervision and in collaboration with Global Project CoordinatorContributes to development programs as required with assistanceCoordinates resources, processes and documentation to meet critical timelinesEnsures compliance to standard operating procedures and guidelinesContributes to the development of new processes and standards

Newmarket

Accountable for coordination, collection and final report of investigation for COVID-19 workplace exposure/outbreakMake decisions which balance and mitigate risk with a clear understanding of the impacts of patient privacy/confidentiality and public safety

Barrie, Ontario

Routinely conduct analysis on issues impacting business operation and proactively identifying opportunities for improvement and overall customer satisfaction and business growth objectives. Thoroughly, budget, document, establish and improve scalability in prospecting, sales meetings and self-effectiveness as a professional to further drive business growth.Maintain close working relationships with customers and key centers of influence in order to leverage relationships to scale prospecting activities.

Peterborough, Ontaraio

Lead continuous improvement initiatives and activities to help develop culture while increasing the efficiency of a staff of 30 members in customer service and satisfaction. Develop training protocols, procedures, and consent forms for staff members and community members to ensure correct product operation and safe operations.Conduct analysis on attendance issues that impacted operational efficiencies and proactively identified and implemented improvement to increase customer satisfaction

Peterborough, Ontario

• Responsible for coordinating and conducting multiple studies with industrial sponsors• Write protocol, develop budgets, prepare Informed Consent forms and all Case Report Forms (CRF)• Prepare and process submissions to Research Ethics Board, including renewals and amendments according to SOPs.• Ensure appropriate study agreements and contracts are in place.• Screen, recruit and randomize eligible patients following proper ICH/GCP• Assure timely completion and submission of Case Report Forms (CRFs) according to Clinical Monitoring Plan or Data Management Plan.• Collect study data and samples.• Process biological samples and ship to Sponsor site using dry-ice.• Ensure proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials.• Monitor and report all adverse events and serious adverse events (AEs & SAEs) as well as all protocol deviations.• Enter data into study database and on Web-based data capture systems; proficient with multiple data capture systems.• Manage data, including ensuring data integrity.• Regularly review the status of the contents of the site Regulatory Binder for each project.• Effectively collaborate and communicate with members of the sponsors, staff from various clinical departments and with other sites in multi-site studies• Manage study budgetary accounts

Hamilton

• Responsible for coordinating and conducting multiple studies focused around lipid and diabetes management for industrial sponsors .• Recruited patients for various cohorts of the study including heart attacks, strokes, and diabetes. • Recruited patients for cross-sectional as well as longitudinal portions of the study.• Meet target numbers for patient recruitment.• Responsible for performing follow up measurements on a timely basis.• Responsible for maintaining databases of patient information such as Medidata Rave, as well as updating patient information on a regular timely basis.• Maintain quality of data collected with high accuracy.• Trained employees on taking proper measurements for the study and data collection and storing.• Trained employees on using specialized equipment for the study.• Train medical students, research fellows in study requirements and help develop project plan and timelines to ensure proper completion of all related studies.• Held training workshop for off-site staff and physicians on proper measuring techniques and procedure as well as data collection.