Heather Campbell, BSc (HK), RCPT(P), CCRC

Experience

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  Centre for Sleep Disorders

  Jan 1997 - Jan 2000

  Technical Director

  • Interviewed, hired and mentored/trained medical, technical and office staff• Contributed to the development and implementation of financial budget• Developed and wrote Policy and Procedure Manuals for the medical and office staff• Created and monitored all quality assurance and infection control programs• Developed and maintained patient database to facilitate patient care, monitor progress and determine outcomes• Responsible for the implementation of educational programs for nursing students, and preparation of staff for certification exams• Conducted sleep studies, analyzed data and completed reports • Educate patients/families on health care needs, conditions, and treatment options• Develop research protocols including recruitment and screening of subjects• Conduct research studies, analyze data and create statistical reports Show less

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  St. Michael's Hospital

  Jan 2000 - Jan 2008

  • Perform full lung function testing; spirometry, plethysmography, single-breath and intra-breath lung diffusion• Conduct Cardio-pulmonary exercise tests, exercise induced asthma tests, methacholine challenges, inspiratory/expiratory pressures, resting/exercise oximetry, and six minute walk tests• Assess response to bronchodilators - pre and post spirometry• Deliver patient education relating to asthma, COPD and inhaler techniques• Accurately perform daily calibrations, ensure proper maintenance of equipment and ensure testing procedures meet with infection control standards Show less

  • Pulmonary Function Technologist/Research Assistant

    Jan 2001 - Jan 2008

  • Team Leader/ Registered Polysomnographer

    Jan 2000 - Jan 2001
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  McMaster University

  Mar 2008 - Mar 2013

  Clinical Research Coordinator

  • Coordinate clinical trials for asthma, allergy and chronic obstructive lung disease in accordance to the study protocol, SOPs and following the international guidelines of Good Clinical Practice (GCP) and ICH • Responsible for high quality data collection, accurate completion of CRFs/eCRFs and timely query resolution• Collection, preparation and submission of regulatory documents to REB and CRO• Collaborate effectively with physicians and other staff members to facilitate appropriate care• Recruit, screen and consent subjects• Perform allergen skin testing by prick and intradermal testing• Execution of allergen induced asthma challenge in human subjects; including titration of allergen dose • Collect, process and handle clinical specimens and biological samples (blood, sputum and urine)• Perform full lung function testing, ECGs and exercise stress tests• Design and maintain organizational tools to conduct the research study accurately in compliance with good clinical practice guidelines• Responsible for the preparation of Initiation, Monitoring, Closure Visits and Study Audits • Perform functions necessary for completion of all research protocols including scheduling, patient enrolment, medical histories, clinical assessments, laboratory-phlebotomy and processing, dispensing of investigational medication and overall organization and logistics of study visits. Show less

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  King's College Hospital NHS Foundation Trust

  May 2017 - Feb 2018

  Respiratory Research Coordinator

  • Coordinate clinical trials for adult and pediatric Cystic Fibrosis patients in accordance to the study protocol, SOPs and following the international guidelines of Good Clinical Practice (GCP) and ICH

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  Evolution Research Group

  Feb 2020 - Oct 2021

  Lead Clinical Research Coordinator

  Here, I delegated tasks effectively to ensure efficient workflow and timely completion of deliverables. I employed quality assurance measures to maintain data integrity and protocol adherence. I identified potential risks and challenges associated with study conduct and develop mitigation strategies to address them proactively. I oversaw planning, implementation, and monitoring of clinical trials by ensuring adherence to study protocols, timelines, and budget constraints.Coordinated trials for ALS, Essential Tremor, Schizophrenia, Mood disorder, Vaccine, and Human Abuse Potential/Human Abuse Liability.Key Successes:• Boosted site profits over the previous year by expanding our clinical trial portfolio to include specialized studies such as ALS, Vaccine trials, and Human Abuse Potential/Human Abuse Liability. Show less

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  Highlands Oncology Group

  Oct 2021 - May 2024

  Coordinate clinical oncology trials in accordance to the study protocol, SOPs and following the international guidelines of Good Clinical Practice (GCP) and ICH • Responsible for high quality data collection, accurate completion of CRFs/eCRFs and timely query resolution• Collaborate effectively with physicians and other staff members to facilitate appropriate care• Recruit, screen and consent subjects • Design and maintain organizational tools to conduct the research study accurately in compliance with good clinical practice guidelines• Responsible for the preparation of Initiation, Monitoring, Closure Visits and Study Audits • Perform functions necessary for completion of all research protocols including scheduling, patient enrolment, medical histories, clinical assessments, and overall organization and logistics of study visits. Show less

  • Clinical Research Supervisor

    Sept 2023 - May 2024

  • Lead Clinical Research Coordinator

    Oct 2022 - Sept 2023

  • Clinical Research Coordinator

    Oct 2021 - Oct 2022
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  Heather M. Campbell Research Consulting

  May 2024 - now

  Clinical Research Consultant