Clinical Research Associate

7 months ago

Richmond, Canada bioLytical Full time

Reporting into the VP, Compliance, the Clinical Research Associate must be a self-starter, 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, and negotiate site budgets and agreements.
- Steer meetings with contract research organization (CRO) and sites around clinical activities, such as:

- Conducting and documenting study monitoring/site visits, coordinating project meetings, and implementing actions for sites that do not meet expectations,
- Overseeing and documenting investigational product dispensing inventory and reconciliation.
- Train and oversee site staff on bioLytical product tests, therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
- Order, track, and manage clinical and trial materials.
- 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 3 years of experience as a Clinical Research Associate. Medical device experience will be an asset.
- 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.
- 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

The annual base salary for this job ranges from:
$65,000-85,000

bioLytical's pay range is based on multiple factors including experience, education, job-related skills, and equity within the team or organization.

**CORE VALUES**

**INNOVATION** in what we do, how we do it and how we think: Contributes new ideas, challenges the status quo, takes the initiative on projects.

**NEVER SAY NEVER**: Stays engaged until the goal is reached or project is completed. Overcomes barriers. Cares so much about the task at hand that the impossible is made possible.

**SENSATIONAL** to our clients, to our partners, to each other: Spirited team player, who adapts to new situations quickly and is beyond reliable.

**TAKES OWNERSHIP** of goals, decisions, actions, and results: Arrives on time and prepared, leads by example, follows through on commitments.

**INSPIRED** to excel: Demonstrates a passion for INSTI, our people and our projects. Is not complacent, shares knowledge freely, exhibits awareness of self, their surroundings, and the business.

\#clinicalresearch #clinicaltrialsmanagement #IVD #medicaldevice #ISO13485

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