Site Activation Partner

This is a fully remote position, open to applicants in Canada.

📋 Description

• Lead or assist with operational tasks from the initiation to the closure of assigned studies and investigator sites.

• Ensure adherence to study timelines, relevant regulations, Good Clinical Practices, and sponsor requirements.

• Initiate and manage activities along with essential document organization for high-quality Investigator Initiation Packages, leading to site initiation authorization.

• Aid in resolving issues and ensure timely escalation of site-related challenges.

• Oversee and collaborate with supporting roles to guarantee prompt site activation and operational tasks.

• Work together with in-country regulatory entities and provide necessary site documents, including those for parallel regulatory authority and ethics submissions.

• Accurately update and maintain clinical trial systems that track site compliance and performance within project deadlines.

• Identify and address issues at investigator sites.

⛳️ Requirements

• High school diploma/certificate with a relevant combination of education, training, and experience.

• Bachelor's degree in life sciences is preferred (BS/BA).

• At least 2 years of relevant experience in a Clinical Trials environment and clinical site activation.

• Experience in the pharmaceutical sector or a Contract Research Organization (CRO) is a plus.

• Understanding of clinical trial methodologies, ICH/GCP, FDA, and both global and local regulations.

• Proficiency in the local language and English.

• Multi-language skills are an advantage.

🏝️ Benefits

• Competitive salary and performance-based incentives.

• Opportunities for professional development and career advancement.

• Comprehensive health and wellness benefits.

• Supportive work environment that values innovation and teamwork.