Parexel Canada is seeking an Experienced Regulatory Affairs Consultant to join its team. This role is ideal for professionals with expertise in regulatory submissions and compliance, particularly in the pharmaceutical, biotechnology, or medical device industries. The position focuses on helping clients navigate complex regulatory requirements across different regions.
Exciting Opportunity for Regulatory Affairs Professionals in Canada!
Are you an experienced regulatory professional ready to take your career to the next level? Parexel is expanding its Regulatory team in Canada, and we’re looking for top talent!
Regulatory Affairs Consultant
Locations: Remote – Canada
What We’re Looking For:
- 6+ years of experience in Clinical Trial Regulatory Affairs
Strong global regulatory affairs leadership skills
Expertise in coordinating complex submissions across multiple countries
*Key Responsibilities:
- Spearhead global regulatory strategies
- Orchestrate Core dossier compilations with global Subject Matter Experts Lead CTA submissions (EU-CTR 536/2014 knowledge preferred)
✔ Location: Eastern Time Zone of Canada preferred
Parexel, a leading clinical research organization, is expanding its Regulatory team in Canada and we are seeking a highly experienced professional to join our talented team. This exciting opportunity calls for an individual with extensive expertise in managing global regulatory strategies and leading a team of local experts. The ideal candidate should possess a passion for regulatory clinical trials and excel in client interactions.
This opportunity at Parexel offers a chance to work with a highly skilled team in a dynamic and growing field, making a significant impact on the regulatory aspects of clinical trials on a global scale.
Due to the nature of the Consultant’s projects, candidates in the Eastern Time Zone of Canada are highly preferred.
Ready to make your mark in the world of regulatory affairs? Apply now
