Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Global Study Manager (Canada)

Job

Insight Global

Wilmington, DE (In Person)

Full-Time

Posted 5 weeks ago (Updated 5 days ago) • Actively hiring

Expires 8/1/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
100
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Job Description Lead and support end-to-end clinical trial delivery from protocol development through closeout May lead smaller projects independently or support a study lead on more complex one Process improvement on how studies are run by gaining expertise on an area of study, sharing best practices, and creating training materials and guidelines Partner cross-functionally with Data Management, Regulatory, Patient Safety, and CRO/external vendor teams to ensure successful study execution Oversee study timelines, budgets, and overall quality to meet key deliverables Develop and manage study plans, protocol documents, and country-specific agreements Track enrollment, data delivery, and study progress; proactively address delays or compliance risks Manage vendor relationships, including scope, performance, and budget oversight Ensure studies are inspection-ready in alignment with ICH-GCP and company SOPs Maintain quality and completeness of the Trial Master File (TMF) Support investigational product supply and logistics across study sites Provide regular updates to stakeholders and leadership while coordinating across global teams Set and manage workload priorities, resources, performance targets and initiatives •Candidates must reside in Canada within an Eastern Time Zone to qualify for this position We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.

To learn more about how we collect, keep, and process your private information, please review
Insight Global's Workforce Privacy Policy:
https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements 3+ years of experience within clinical trials for a life sciences/pharmaceutical organization Oncology experience Leadership experience supporting the timeline, budget, and overall execution of clinical trials from inception to completion Experience running daily team meetings, tracking progress, and coordinating with different teams on a global scale Strong documentation skills including maintenance of TMF and CTMS systems Solid knowledge and understanding of the clinical study and drug development processes, GCP/ICH guidelines Experience working with CROs and external vendors in a strategic level Mentorship experience Bachelors Degree in life sciences or related field