Bio-K+ International Inc.
Chez Bio-K Plus International Inc. nous sommes passionnés par la santé et le mieux être des gens.
Nous offrons des opportunités de carrière passionnantes en…
Provide administrative support to clinical projects under direction of line manager, Clinical Research Specialist and/or other designated clinical team members.
The Health Access and Outcomes team is focused on providing services for Market Access, HEOR, and medical, scientific teams.
Conduct ad-hoc project tasks.
Uploading and tracking regulatory documents, file reviews.
Ad hoc requests such as meeting minutes, CRA and site contact, sending supplies and binders to sites.
You will learn the life-cycle of a clinical trial and play an integral role in maintaining the quality and regulatory compliance of study deliverables.
Maintains reference files needed by production database and report development.
Develops an understanding of the knowledge needed to maintain reference files.
The Regulatory Affairs Associate will be primarily responsible for the complication and filing of new regulatory submissions for new products with Health Canada…
As a Data Scientist Programmer with balanced analytics, technology, and consulting experience, you will provide data analytics expertise to
IQVIA R&D Solutions'…
Serve as primary point of contact for customer on data management deliverables.
Provides clinical lab data expertise as part of a team to develop and maintain…
The person in this role is responsible for the on-time completion of projects or components of medium to large projects for clients in the pharmaceutical or…
The FP&A Partner will be responsible for supporting the Canadian affiliate on various Finance tasks for all UCB products within Canada; currently two…
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