Junior Clinical Trials Document Analyst Job Vacancy in IQVIA Ottawa, ON – Latest Jobs in Ottawa, ON
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Company Name : IQVIA
Location : Ottawa, ON
Position : Junior Clinical Trials Document Analyst
Job Description : We are looking for a Junior Clinical Trials Document Analyst within IQVIA’s Privacy Analytics’ team in Ottawa, Canada. For more information about Privacy Analytics, please visit us at https://privacy-analytics.com
Our Clinical Trials Transparency (CTT) team is growing. We’re hiring a Junior Clinical Trials Document Analyst to support an expanding line of business. In this role you’ll be end-to-end responsible for anonymization projects of client documents. Using our tools you will analyze and mitigate the risk of re-identification for trial participants whose data appears in clinical trials documentation. As an ideal candidate you learn quickly and can produce extremely accurate, precise work within tight timelines. You’re familiar with medical / healthcare language, comfortable with numbers, and your excellent communication skills are complemented by strong technical acumen and the ability to meet tight deadlines.
In this job you will:
Develop familiarity with our de-identification methodology.
Own assigned projects or project tasks and deliver such on time and with the required quality, providing timely and transparent status updates and managing client expectations.
Process clients’ clinical trials documents and data. Core responsibilities here include: Pre-processing documents, analyzing lengthy, technical / medical documents (Clinical Study Reports), checking the quality of automated document processing steps and manually securing patient and commercial information where required
and / or:
Identify and classify direct and indirect identifiers, measure and mitigate re-identification risk, determine and apply required transformations.
Facilitate the creation of anonymization reports and other client deliverables.
Collaborate closely with other team members, ensuring that all work meets established quality standards and is completed on time. Participate in peer-reviews of work products.
Identify and communicate tool enhancements/refinements and relate defect documentation to developers and researchers.
To do this you will have:
A Bachelor’s degree in Healthcare or Statistics or similarly related field
The ability to read, review and analyze clinical trial documents, ideally familiarity with clinical trial documents, clinical study reports (CSRs).
The ability to learn our methodology and develop a thorough understanding of how directly and indirectly identifying information contributes to the risk of re-identification.
Exceptional detail-orientation.
Well-developed communication and interpersonal skills.
The drive to meet exacting deadlines and the flexibility to adapt to shifting priorities.
Ability to manage sensitive information with the utmost confidentiality.
Experience with Adobe PDF and MS Office products (Excel, Word, and PowerPoint) required
Nice to have / beneficial assets:
ICH guidelines for clinical trial documents and EMA Policy 0070 or Health Canada are valuable assets.
Ability to understand and navigate MedDRA terms and their hierarchy.
Medical writing or trial data programming experience.
Office Address: Laurier Ave W #200, Ottawa, ON K1P 5J6, Canada.
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
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