As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects rights safety and well-being and quality of data compliance.
Home-based in Quebec Canada.
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review source document verification and query resolution
- Be responsible for site communication and management
- Supervise study activities timelines and schedules on the country level
- Be a point of contact for in-house support services and vendors
- Be involved in quality control such as compliance monitoring and reports review
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Qualifications :
- College/University degree in Life Sciences or an equivalent combination of education training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Participation in clinical projects as a Lead/Senior Monitor
- Experience in Oncology
- Full working proficiency in English and French
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problem-solving skills
- Ability to travel
- Valid drivers license (if applicable)
Additional Information :
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
Remote Work :
Yes
Employment Type :
Full-time
As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus ...
As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects rights safety and well-being and quality of data compliance.
Home-based in Quebec Canada.
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review source document verification and query resolution
- Be responsible for site communication and management
- Supervise study activities timelines and schedules on the country level
- Be a point of contact for in-house support services and vendors
- Be involved in quality control such as compliance monitoring and reports review
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Qualifications :
- College/University degree in Life Sciences or an equivalent combination of education training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Participation in clinical projects as a Lead/Senior Monitor
- Experience in Oncology
- Full working proficiency in English and French
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problem-solving skills
- Ability to travel
- Valid drivers license (if applicable)
Additional Information :
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
Remote Work :
Yes
Employment Type :
Full-time
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