20 meilleures offres (clinical trial, vancouver bc) (à pourvoir)

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Alimentiv —Vancouver, BC
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Coordinator, Research Data Management - BC Children’s Hospital Research Institute
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Clinical Trials Manager (12-month contract)
Zymeworks Inc. —Vancouver, BC
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Research Projects Coordinator 2, Basic & Translational Research Genome Sciences Centre (GSC)
BC Cancer —Vancouver, BC
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Clinical Trials Nurse Coordinator, Research Clinical Trials - BC Cancer - Vancouver
BC Cancer —Vancouver, BC
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Assistant Manager, Human Resources (VCHRI)
University of British Columbia —Vancouver, BC
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Senior Program Manager (Clinical)
Zymeworks Inc. —Vancouver, BC
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il y a 7 jours
Patient Recruitment Specialist
Headlands Research —Richmond, BC
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Assistant Manager, Human Resources (VCHRI)
UBC Faculty of Forestry —Vancouver, BC
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il y a 13 jours
Clinical Trials Nurse Coordinator. Personalized Oncogenomics (POG) Team - BC Cancer Vancouver
BC Cancer —Vancouver, BC
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Discovery Operations Coordinator
Xenon Pharmaceuticals —Burnaby, BC
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il y a 4 jours

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Associate, Clinical Research

bioLytical -
Richmond, BC

Postuler dès maintenant

Détails du poste

Temps plein
De 68 000 $ à 80 000 $ par an

Profil recherché

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Office
Baccalauréat
Compétences en informatique
Collecte de données
Compétences en communication

Description complète du poste

bioLytical is hiring an experienced Clinical Research (CR) Associate. You will support clinical operations and assist in the planning, development, and implementation of multiple studies in support of bioLytical’s product portfolio. Working closely with the Vice President, Compliance, the CR Associate must be able to recognize logistical problems, initiate appropriate solutions, proactively identify, resolve/mitigate, and escalate issues on matters relating to clinical trial requirements, clinical evaluations and bioLytical product related publications.

Specifically, you will support clinical site activations and ongoing monitoring, with frequent travelling (50%) required.

You will play a vital role in driving forward our mission to get people tested with the best technology on the market, living the Core Values through and through.

HOW YOU WILL CONTRIBUTE

Demonstrate and integrate bioLytical product knowledge to design, create and write trial protocols and study documentation including ethics applications for bioLytical products and liaising with regulatory authorities.
Conduct data analysis, compile and generate scientific reports, regulatory documentation, and research-related documents.
Ensure study sites and activities adhere to appropriate industry protocols and terms of study.
Train and oversee site staff on bioLytical product tests, therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.
Conduct and document study monitoring/site visits, coordinate project meetings and implement actions for sites do not meeting expectations.
Order, track, and manage clinical and trial materials.
Oversee and document investigational product dispensing inventory, and reconciliation
Protect subjects’ confidentiality, update information, and verify IP have been dispensed and administered according to protocol.
Oversee study database design and management.
Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines.

WHAT YOU WILL BRING

Bachelor’s degree in Biological Science or a related field.
Minimum 3 years of experience in clinical operations.
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.
Travel to clinical sites globally (50%).

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!
Full-size in-house fitness gym and shower facilities
Complimentary reserved parking
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:

$68,000-$80,000

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

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.

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 #protocolwriting #medicaldevice #ISO13485 #ISO14971 #clinicaloperations #regulation #USFDA

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