Clinical Research Associate

i-Pharm ConsultingGruppe; Canada; On-site; CAD 70,000 - 90,000; Full time

Job summary

A leading biopharmaceutical services organization in Canada is seeking a skilled Clinical Research Associate II with oncology experience. This home-based role involves monitoring clinical trial sites to ensure compliance with protocols and regulatory requirements. Qualified candidates should have at least 2 years of clinical monitoring experience and be bilingual in French and English, especially for the Montreal location. Competitive compensation and opportunities for growth are included.

Qualifications

• Minimum 2 years of clinical monitoring experience in oncology trials.
• Strong knowledge of GCP and ICH guidelines.
• Ability to travel extensively (approximately 65-85%) as required.

Responsibilities

• Conduct monitoring visits in alignment with GCP standards.
• Collaborate with sites to support patient recruitment.
• Track study progress including regulatory submissions.

Skills

Clinical monitoring

Communication skills

Problem-solving skills

Organizational skills

Bilingual (English/French)

Education

Bachelor’s degree in life sciences or healthcare

Tools

Microsoft Office

Electronic data capture systems

Job description

Clinical Research Associate II – Oncology

Location: Home-based in Toronto, Vancouver, Montreal

Travel: Travel required for investigator site visits

Employment Type: Full-time / Permanent

Language Requirement: Bilingual in French & English (Required in Montreal)

We are seeking a skilled and motivated Clinical Research Associate II with oncology experience to join a leading biopharmaceutical services organization. This role involves monitoring and managing clinical trial sites to ensure compliance with protocols, regulatory requirements, and sponsor expectations.

We are currently hiring for 3 different locations: Toronto, Vancouver, Montreal (bilingual French/English)

Key Responsibilities

• Conduct monitoring visits including site initiation, routine monitoring, and close‑out visits in alignment with Good Clinical Practice (GCP) standards.
• Collaborate with clinical sites to support patient recruitment and study execution.
• Administer protocol and study‑related training to site staff and maintain ongoing communication.
• Evaluate site compliance with study protocols and regulatory guidelines; identify and report quality issues.
• Track study progress including regulatory submissions, patient enrollment, data collection, and query resolution.
• Ensure proper documentation and maintenance of regulatory and study files.
• Work closely with study teams and provide timely reports and documentation.
• Support financial and contractual site activities as applicable.

Qualifications

• Bachelor’s degree in a life sciences or healthcare discipline.
• Minimum 2 years of clinical monitoring experience, preferably in oncology clinical trials.
• Strong knowledge of GCP and ICH guidelines.
• Bilingual in English and French is highly preferred.
• Excellent organizational, communication, and problem‑solving skills.
• Proficient in Microsoft Office applications and electronic data capture systems.
• Ability to travel extensively (approximately 65‑85%) as required.
• Valid driver’s license.

Additional Information

• This role requires residency in the country of employment.
• Candidates must demonstrate the ability to work independently and collaboratively with global study teams.

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