At a Glance
- Tasks: Conduct site visits and ensure compliance with clinical trial regulations.
- Company: Join TRIO, a global leader in cancer research and clinical trials.
- Benefits: Enjoy competitive salary, flexible hours, and generous vacation time.
- Other info: Remote work opportunity with excellent growth potential and supportive team culture.
- Why this job: Make a real difference in cancer treatment while advancing your career.
- Qualifications: Bachelor's degree in health fields and 2 years of CRA experience required.
The predicted salary is between 100000 - 122500 $ per year.
Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to the CRA Line Manager, this position will be remote based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba). This is an upcoming vacancy, and we are currently accepting applications.
Responsibilities:
- Conducting site visits, including pre-study, initiation, monitoring and termination;
- Confirming adherence to all FDA, ICH-GCP and local regulations;
- Ensuring the completion and collection of regulatory documents;
- Performing data verification of source documents;
- Ensuring implementation and compliance with FDA, ICH-GCP guidelines;
- Participating in budget negotiation and follow-up where applicable;
- Assisting with data validation and query resolution;
- Mentoring junior team members as required.
Qualifications:
- Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science – or its international equivalent
- Minimum 2 years of previous CRA experience
- Experience monitoring phase 1 trials
- Excellent knowledge of medical terminology and clinical monitoring process
- Strong ICH-GCPs knowledge
- Experience with clinical trial information systems
- Ability to travel up to 60% on average
- Must work both independently and in a team environment
- Read, write and speak fluent English required
- French is desirable but not required
What TRIO Can Offer You:
- Annual compensation review with opportunities for professional growth
- 3 weeks of vacation plus paid December Holiday Closure
- 10 days paid personal/sick time
- 1 paid volunteer day / year
- A rich benefit plan with Health, Dental, Vision & Life Insurance premiums paid by TRIO
- Up to 5% RRSP Matching Program
- Flexible working hours to promote work-life balance
- Monthly Internet Allowance to support working from home
- One-time Home Office Allowance
- Maternity Leave Top-Up Program
- Employee Family Assistance Program to support you and your family during difficult times
- Employee Referral Bonus Program
Pay Range: $100,000.00 to $122,500.00 - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
Teamwork · Passion · Integrity · Innovation
Clinical Research Associate in Vancouver employer: Translational Research in Oncology
At Translational Research in Oncology (TRIO), we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our remote, freelance Clinical Research Associate position offers the flexibility to work from anywhere in Western Canada while contributing to groundbreaking cancer research. With a strong commitment to employee growth, we provide opportunities for mentorship and professional development, ensuring that our team members are equipped to make a meaningful impact in the fight against cancer.
Contact Details:
Translational Research in Oncology Recruitment Team
