Senior Clinical Research Associate
PSI CRO Open At a glance
Senior role at PSI CRO. Remote, Canada · full-time · CA$120,000–CA$150,000 base.
remoteroles summary, based on the employer's posting.
What you'll do
- Run and document SIV, RMV and COV monitoring visits at study sites
- Check case report forms against source records and resolve resulting data queries
- Manage site communications, coordinate with support teams and vendors, and update project colleagues on study progress
- Help assess study feasibility and prepare regulatory submission materials
- Support audits and inspections by helping prepare for them and taking part
What you bring
- A college or university qualification in life sciences, or comparable education, training and experience
- You have independently monitored sites and handled the different visit types in Phase II or Phase III studies
- You work fluently in English, can use MS Office, and hold a valid driver’s license
- You can plan competing tasks, travel, and work collaboratively to solve problems
Who this fits
This freelance senior CRA role suits someone with independent site-monitoring experience who can travel for on-site visits. You must be able to work in Canada without needing employment visa sponsorship now or later. Oncology experience is a plus.
From the employer
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:
- Conduct and report SIV, RMV, COV onsite monitoring visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare and particiapte on audits and inspections
- 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
- Experience in Oncology is a plus
- Full working proficiency in English.
- 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 driver’s license
For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
Other work from LinkedIn, X, Reddit and Upwork, in one list.
Each morning you get everything that fits, strongest first.
OtherRemote
Find me workBy the team behind remoteroles.