Clinical Study Lead — Flexible Schedule & Remote Options

BioTalent Canada; Quebec; Hybrid; CAD 70,000 - 90,000; Full time

Job summary

A dynamic biotech company is seeking a Clinical Study Manager in Quebec, Canada. The successful candidate will oversee clinical studies, ensuring compliance with GCP standards, while collaborating with internal and external teams. This role requires at least 3 years of clinical operations experience, strong communication skills, and a scientific background. Benefits include flexible hours and remote work options. Interested applicants should contact Catherine Lippé at [e-mail].

Benefits

Flexible schedule between 6:00 AM and 6:00 PM

Optional remote work two days a week

Employee assistance program

Group RRSP

Eligibility for annual bonus

Vacation and wellness days

Positive work culture

On-site parking

Qualifications

• At least 3 years of prior clinical operations experience, preferably with CRO/small biotech.
• Must work independently and as an integral team member.
• Strong organizational and analytical skills.

Responsibilities

• Accountable for operational aspects of assigned clinical studies.
• Develop, maintain, and manage study timelines.
• Ensure studies comply with FDA, EMEA, GCP, and ICH guidelines.

Skills

In-depth knowledge of Good Clinical Practice (GCP)

Familiarity with standard clinical operating procedures

Excellent verbal and written communication skills

Strong working knowledge of Microsoft Project, Excel and PowerPoint

Bilingual (English and French)

Education

BSc/BA in a scientific-related field

Job description

A dynamic biotech company is seeking a Clinical Study Manager in Quebec, Canada. The successful candidate will oversee clinical studies, ensuring compliance with GCP standards, while collaborating with internal and external teams. This role requires at least 3 years of clinical operations experience, strong communication skills, and a scientific background. Benefits include flexible hours and remote work options. Interested applicants should contact Catherine Lippé at [e-mail].