Site Activation Manager

🔥 1 minute ago

🇨🇦 Canada – Remote

💵 $103k - $137.3k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Direct and manage strategic, operational, and financial delivery of Site Activation activities • Provide strategic planning and project oversight to accelerate site activation and patient enrollment • Support and/or participate in pre-award and bid defense activities • Oversee study start-up from pre-award through site activation and/or lifecycle maintenance • Manage multiple regions or global Site Activation Management projects • Develop, implement, and maintain Site Activation Management Plans • Collaborate with internal and external stakeholders, regions, and countries • Execute strategies for clinical study approvals, authorizations, contracts, and essential documents • Assess regulatory landscapes and provide regulatory intelligence • Determine regulatory strategies and parameters for submissions and authorizations • Provide updates and reports to study teams and senior colleagues • Maintain internal systems, databases, tracking tools, timelines, and project plans • Create and/or review technical and administrative documentation • Adhere to quality, regulatory, and company standards throughout trials • Mentor and coach colleagues • Develop and maintain relationships with preferred IQVIA customers • Deliver presentations and training to clients, colleagues, and professional bodies • Contribute to departmental and organizational initiatives

🎯 Requirements

• Bachelor's Degree in Life Sciences or related field (required) • At least 5 years of experience, including 2 years of lead experience, in a scientific or clinical environment (required) • Demonstrable experience in an international role, or equivalent combination of education, training and experience (required) • Must reside in the same country/sales region where the job is located • Knowledge of ICH-GCP, protocols, customer requirements, internal policies, regulatory requirements, site activation, ethics and regulatory processes, and site contracting

🏖️ Benefits

• Incentive plans, bonuses, and/or other forms of compensation may be offered • Health and wellness benefits • Other benefits