Senior Clinical Research Associate

Translational Research in Oncology; Old Toronto; Remote; CAD 125,000 - 143,000; Full time

Job summary

A global clinical research organization is seeking a Senior Clinical Research Associate (CRA) specializing in oncology. This remote position involves conducting site visits, ensuring compliance with regulations, and mentoring junior team members. Join a dedicated team focused on advancing cancer research.

Benefits

Annual salary reviews

3 weeks of vacation

Comprehensive benefits including Health, Dental, Vision, and Life Insurance

Flexible working hours

Monthly internet allowance

Home Office Allowance

Maternity and Parental Leave Top-Up

Employee Assistance and Recognition Programs

Qualifications

• Minimum 5 years of CRA experience, with at least 2 years in oncology trials.
• Ability to travel up to 60%.

Responsibilities

• Conduct site visits, including pre-study, initiation, monitoring, and termination.
• Ensure adherence to FDA, ICH-GCP, and local regulations.

Skills

Oncology knowledge

Medical terminology

Clinical monitoring processes

Teamwork

Mentoring

Education

Bachelor's Degree in Medical, Nursing, Pharmacy, or related health sciences

Tools

Clinical trial information systems

Job description

Job Opening: Senior Clinical Research Associate (CRA) - Oncology

If you are an experienced Senior CRA passionate about oncology research and eager to join a highly skilled team, TRIO offers an excellent opportunity for you!

Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research through clinical trials. Our team is committed to delivering innovative cancer treatments to the world today.

We are seeking a Senior Clinical Research Associate to join our international team. This remote-based position in Canada reports to a CRA Line Manager.

Responsibilities:

1. Conduct site visits, including pre-study, initiation, monitoring, and termination;
2. Ensure adherence to FDA, ICH-GCP, and local regulations;
3. Manage regulatory documents and ensure their completion and collection;
4. Perform data verification of source documents;
5. Implement and ensure compliance with FDA, ICH-GCP guidelines;
6. Participate in budget negotiations and follow-up where applicable;
7. Assist with data validation and query resolution;
8. Mentor junior team members as required.

Qualifications:

• Bachelor's Degree in Medical, Nursing, Pharmacy, or related health sciences, or an international equivalent;
• Minimum 5 years of CRA experience, with at least 2 years in oncology trials;
• Advanced oncology knowledge;
• Excellent understanding of medical terminology and clinical monitoring processes;
• Strong knowledge of ICH-GCP guidelines;
• Experience with clinical trial information systems;
• Ability to travel up to 60%;
• Ability to work independently and as part of a team;
• Fluent in English (reading, writing, speaking);
• Ability to mentor and train junior CRAs effectively.

What TRIO Offers:

• Annual salary reviews with growth opportunities;
• 3 weeks of vacation plus paid December Holiday Closure;
• 10 days paid personal/sick leave;
• One paid volunteer day per year;
• Comprehensive benefits including Health, Dental, Vision, and Life Insurance;
• Up to 5% RRSP matching program;
• Voluntary TFSA program;
• Flexible working hours for work-life balance;
• Monthly internet allowance for remote work;
• Work arrangement options (Office, Hybrid, Home-based) with a one-time Home Office Allowance;
• Mobile phone stipend for qualifying roles;
• Option to work internationally for short periods;
• Maternity and Parental Leave Top-Up;
• Employee Assistance and Recognition Programs;
• Referral Bonus Program;

Pay Range: $125,000 - $142,500, influenced by education, experience, location, and skills.

Join us and embody our core values: Teamwork, Passion, Integrity, Innovation.