At a Glance
- Tasks: Review, draft, and manage Technical Documents for EU MDR compliance.
- Company: Join ClinChoice Canada Inc., a global leader in regulatory affairs.
- Benefits: 12-month contract with competitive pay and professional growth opportunities.
- Other info: Collaborative environment with a focus on accuracy and timely delivery.
- Why this job: Make a real impact in the regulatory landscape while working with a dynamic team.
- Qualifications: 2+ years in Regulatory Affairs, knowledge of EU MDR, ISO13485, and FDA regulations.
The predicted salary is between 82800 - 101200 $ per year.
Clin Choice Canada Inc. is seeking a Sr.
Regulatory Affairs Associate – CONSULTANT to join its global CRO team on a 12‑month contract.
You will work closely with regulatory project teams to review, draft, and manage Technical Documents for EU MDR and other regulatory needs, ensuring accuracy and timely delivery.
The role requires at least 2 years in Regulatory Affairs focused on EU MDR, knowledge of ISO13485 and FDA regulations, and strong English communication.
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Senior Regulatory Affairs Consultant – EU MDR Expert in Winnipeg employer: ClinChoice
ClinChoice Canada Inc. is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the clinical data management field. With a strong emphasis on employee growth and development, team members are encouraged to enhance their skills through ongoing training and mentorship opportunities. Located in Ontario, the company offers a hybrid work model that promotes work-life balance while contributing to impactful clinical trials.
