Oncology Study Delivery Associate (Hybrid - Mississauga)

Résumé du poste

The associate will assist in the coordination and administration of clinical trials while ensuring compliance with protocols and regulatory requirements. They will also maintain essential study documentation and collaborate with cross-functional teams to facilitate smooth trial execution.

Détails du poste

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. What you will be doing Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. Support the preparation of study-related materials, such as informed consent forms and case report forms. Work with cross-functional teams to facilitate communication and ensure smooth trial execution. Contribute to the tracking and reporting of clinical trial metrics and milestones. Your profile Bachelor's degree in a scientific or healthcare-related field. Two years experience in Clinical Research or an appropriate mix of educational/professional experience Must have a strong understanding of regulatory documentation Knowledge of clinical trial processes, regulations, and guidelines. Excellent organizational and communication skills. Prior experience or strong interest in clinical research. Oncology experience required Must be comfortable with a hybrid role (office/home) in Mississauga Canada Ability to work collaboratively in a fast-paced environment with attention to detail. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply.

Ce que vous ferez

The associate will assist in the coordination and administration of clinical trials while ensuring compliance with protocols and regulatory requirements. They will also maintain essential study documentation and collaborate with cross-functional teams to facilitate smooth trial execution.

Exigences

Candidates must possess a bachelor's degree in a scientific or healthcare-related field and at least two years of experience in clinical research. Strong knowledge of regulatory documentation, oncology experience, and the ability to work in a hybrid environment in Mississauga are required.

Avantages

• Competitive base salary • Performance related incentives • Medical coverage • Dental coverage • Vision coverage • Retirement and pension plans • Life assurance • Disability coverage • Employee assistance programmes • Wellbeing resources • Learning and development opportunities

Compétences indiquées

• Regulatory Compliance · Souhaitée
• Communication · Souhaitée
• Cross-Functional Collaboration · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical research
• Oncology
• Regulatory documentation
• Clinical trial coordination
• Regulatory compliance
• Study file maintenance
• Informed consent forms
• Case report forms
• Clinical trial metrics
• Communication
• Organizational skills
• Cross-functional collaboration

Domaines d’emploi

• Science & Research
• Healthcare
• Consulting