Study Manager - Oncology - Home Based (US or Canada)

PRA Health Sciences; Canada; Remote; CAD 70,000 - 100,000; Full time

Job summary

Join a leading clinical research organization as a Study Manager, where you'll oversee the operational conduct of clinical studies and interact with stakeholders. This role requires a BS/BA/MS/PhD and offers a competitive salary and diverse benefits tailored to your needs.

Benefits

Various annual leave entitlements

Health insurance options

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• 2+ years of clinical research experience required.
• Experience in pharmaceutical and/or clinical drug development beneficial.
• Legal authorization to work in the US or Canada.

Responsibilities

• Assist with operational conduct of clinical studies.
• Track study timelines and utilize project management tools.
• Interact with stakeholders to support clinical study objectives.

Skills

Communication

Project Management

Clinical Research

Excel

PowerPoint

Education

BS / BA / MS / PhD

Job description

Join Our Team as a Study Manager

As a Study Manager, you will be part of the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What you will be doing:

• Assist the SM Study Lead and study team with the operational conduct of clinical studies, including activities such as CTT minutes, clinical supplies planning and tracking, lab specimen tracking, imaging data reconciliation, status update reports, and study closeout activities.
• Support a single study or multiple studies.
• Lead a study with limited scope (e.g., Survival Follow-up).
• Track study timelines and utilize project management tools proficiently.
• Interact with internal and external stakeholders (study sites, vendors, committees, etc.) to support clinical study objectives.

Qualifications

What you need to have:

• Educational Requirements: BS / BA / MS / PhD with 2+ years of clinical research experience.
• Experience in pharmaceutical and/or clinical drug development is beneficial but not required.
• Oncology experience is beneficial but not required.
• Strong oral and written communication skills.
• Proficiency in Excel and PowerPoint.
• Legal authorization to work in the United States or Canada without the need for future sponsorship.

Home based in US or Canada.

What ICON Can Offer You

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

• Various annual leave entitlements.
• A range of health insurance options to suit you and your family’s needs.
• Competitive retirement planning options.
• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to over 80,000 professionals.
• Life assurance.
• Flexible country-specific benefits, including childcare vouchers, bike schemes, gym memberships, travel passes, and health assessments.

Visit our careers website to learn more about working at ICON.

Diversity & Inclusion

At ICON, diversity, inclusion & belonging are fundamental. We are committed to an inclusive environment free of discrimination and harassment. All qualified applicants will receive equal consideration for employment.

If you need a reasonable accommodation during the application process or to perform the essential functions of the role, please let us know.

Interested?

We encourage you to apply regardless of whether you meet all the requirements — you might be exactly who we're looking for.