Clinical Research Associate

Reporting into the VP, Compliance, the Clinical Research Associate must be able to recognize logístical problems, initiate appropriate solutions, proactively identify, resolve/mitigate, and escalate issues on matters relating to clinical trial requirements, clinical evaluations and product related publications.

**About bioLytical**

bioLytical Laboratories Inc. is a privately-owned Canadian company focused on the research, development and commercialization of rapid in-vitro medical diagnostics using its proprietary INSTI® technology platform. bioLytical has won several local and industry awards, including BC Exporter of the Year in 2019 and the Globe and Mail’s Fastest Growing Companies list in 2020. We have been named Lifesciences BC’s Growth Stage Med Tech Company of the Year and have been featured on BC’s Fastest Growing Companies six years in a row. bioLytical moved to a significantly larger, state-of-the-art facility in Richmond in 2020 to accommodate the extraordinary growth achieved through our team.

**HOW YOU WILL CONTRIBUTE**
- Identify, evaluate, establish, and close trial sites, negotiate site budgets and agreement.
- Supervise study sties and activities to ensure adherence to appropriate industry protocols and terms of study.
- Train and oversee site staff on INSTI tests, therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
- Conduct and document study monitoring/site visits, coordinating project meetings and implementing actions for sites do not meeting expectations.
- Order, track, and manage clinical and trial materials.
- Oversee and document investigational product dispensing inventory, and reconciliation.
- Oversee study database design and management.
- Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines.

**WHAT OUR IDEAL CANDIDATE WILL HAVE**
- Bachelor’s degree in Biological Science or a related field.
- Minimum 5 years of experience as a Clinical Research Associate.
- Knowledge of the diagnostics industry, terminology, and practices and FDA regulations and their practical implementation.
- Strong background in statistical data collection, validation, editing and analysis techniques.
- Superior problem solving, deductive reasoning and decision-making skills.
- Strong verbal and written communication skills.
- Proficient computer skills, with Microsoft Office Word, Excel, and PowerPoint.
- Good time management and ability to prioritize task and accomplish set goals efficiently.
- Available to travel extensively and on short notice, and ability to manage travel schedules. (Post-COVID)
- Experience liaising with Regulatory Authorities i.e. US FDA, Health Canada, Notified Bodies will be an asset
- Knowledge of Canadian, US and European regulations, ISO 13485 and ISO 14971 will be an asset.
- Please note that this position is an on-site role based out of our Richmond, BC facility.

**WHAT WE OFFER**
- A competitive compensation package
- Extended health benefits including dental - 100% employer contribution
- Flexible working hours
- Paid sick days
- Bonus day off with pay on your birthday every year
- Complimentary reserved parking
- Exercise room with a gym and shower facilities
- Opportunity to work with industry experts who are motivated and passionate about what they do but know how to have some fun
- A chance to show off your dance moves and singing voice at the company parties and jump in to score a victory or lead the way in our outdoor games at the summer barbeques
- The opportunity to join an ‘off the charts’ foodie culture in our large kitchen and try out your favourite recipes or enjoy the culinary delights as they hit the share table