Senior Project Set-Up Coordinator – Laboratory Services

🔥 26 minutes ago

🇨🇦 Canada – Remote

💵 $62.1k - $103.5k / year

⏰ Full Time

🟠 Senior

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Assist with study validation activities • Research and resolve issues, gather relevant information, and liaise with laboratory teams to ensure projects are set up according to procedures and customer requirements • Configure project databases, where applicable • Maintain complete, accurate, and up-to-date project documentation • Keep Set-Up Managers, Project Managers, and stakeholders informed of issues affecting project execution • Coordinate planning and handover meetings with colleagues and internal departments • Participate in local and global continuous improvement initiatives • Participate in internal audits, as required • Communicate with study sponsors and exchange factual information • Assist in developing database design requirements for study protocols and amendments • Contribute to project planning, timeline development, regulatory milestone tracking, and risk identification • Manage the set-up process for low-complexity studies, where applicable • Mentor and assist in training less experienced staff • Perform activities in accordance with the ICH E6 Guideline for Good Clinical Practice (GCP)

🎯 Requirements

• Bachelor’s degree in Life Sciences or a related field preferred; an equivalent combination of education, training, and experience may be considered in lieu of a degree • Minimum of one year of relevant experience in the Clinical, Medical, or Healthcare industry, or an equivalent combination of education, training, and experience • Strong organizational and coordination skills • Demonstrated commitment to quality, accuracy, and attention to detail • Strong verbal and written communication skills • Proficiency with computer applications, including word processing and spreadsheet software • Knowledge of Clinical Trial Management Systems (CTMS) preferred • Ability to work effectively in a fast-paced environment and manage multiple priorities • Ability to establish and maintain effective working relationships with colleagues, managers, and clients • Knowledge of laboratory processes and computer systems considered an asset • Functional proficiency in written and spoken English required

🏖️ Benefits

• Incentive plans, bonuses, and/or other forms of compensation may be offered • Health and wellness benefits • Equal opportunity employer • Disability accommodations available throughout the recruitment process

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