Medical Device Clinical Consultant jobs
Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $46,563.40–$60,000.00 a year
- Full-time
- Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements,…
View similar jobs with this employerMedical Device Sales Consultant
Easily applyNewDynasplint Systems, IncHamilton, ON- $45,000–$50,000 a year
- Full-time +1
- Paid time off
- Preferred fields of study physical/athletic therapy, kinesiology, sports science or a related subject with knowledge of anatomy.
- Training provided in Canada/US.
Senior Medical Writer
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $90,000–$140,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Excellent understanding of clinical trials and common clinical trial statistical analysis methods (preferred).
- Plan and carry out professional development.
Senior Medical Writer
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $90,000–$140,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Excellent understanding of clinical trials and common clinical trial statistical analysis methods (preferred).
- Plan and carry out professional development.
Manager, Clinical Data Management
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $140,000–$170,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Demonstrated ability to effectively manage medical information and organize and integrate the activities of information processing personnel.
- GenentechOceanside, CA
- Full-time
- Experience & Education: BS/MS/PhD in Science, Engineering or Management with at least 8 years of experience in the pharmaceutical, biopharmaceutical or medical…
Consultant Cardiologist (Special Interest in Device Therapy)
Easily applyMultiple openingsHealthy Heart InstituteRed Deer, AB T4N 3Z6- $400,000–$600,000 a year
- Full-time +2
- On call
- Minimum 20+ years of consultant-level experience in tertiary and district general hospitals, including establishment of EP/device services.
Consultant en implantation / Senior Implementation Consultant, Sage Intacct (bilingue)
Easily applyUrgently hiringVision33Ontario- Full-time
- Paid time off
- Company pension
- Paid vacation
- Wellness program
- Vision33 est une firme mondiale de services de conseils professionnels en informatique qui résout les défis commerciaux des clients grâce à des services de…
Product Development Specialist III
Easily applyAgile MVMontréal, QC- Full-time +1
- Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
- Job Types: Full-time, Permanent.
- Southmedic Inc.Barrie, ON L4M 5K3
- $100,000–$125,000 a year
- Permanent
- Mileage reimbursement
- Tuition reimbursement
- Vision care
- Dental care
- Employee assistance program
- RRSP match
- Benefits - Our group benefit plan covers medical, dental, vision, and other health needs, including our employee assistance program.
- Syneos - Clinical and Corporate - ProdRemote
- Full-time
- Coordinate the necessary medical/scientific input from outside experts/consultants/advisors.
- Thorough knowledge of Regulatory requirements andthe clinical…
Lead Consultant (Hybrid)
Easily applyOften replies in 1 dayQ&C ServicesMississauga, ON L5N 1V8- $70,000–$85,000 a year
- Full-time +1
- Paid time off
- Vision care
- Dental care
- Life insurance
- Employee assistance program
- Profit sharing
- This position may require onsite consultant engagements with in the pharmaceutical industry.
- This pharmaceutical consultant role focuses on applying your GMP…
Industry Consultant, Healthcare Services Sales
Easily applyRicoh CanadaMississauga, ON- $100,000–$105,000 a year
- Full-time +1
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- RRSP match
- Extended health care
- The ISS will demonstrate a high degree of business acumen, technical knowledge, communication skills as well as a proven track record of driving high valued…
Outside Sales Representative
Easily applyOften replies in 1 dayEvolve Business GroupToronto, ON M5V 2Y6- $90,000–$150,000 a year
- Freelance
- Proven success in medical device or surgical supply sales.
- Build your reputation and business in a niche medical market with strong demand.
Strategic Advisor / Senior Consultant
Easily applyBevertecToronto, ON M7A 2E5- 10+ years of experience in healthcare strategy, digital transformation, or management consulting.
- Strong knowledge of Ontario healthcare and digital health…
View similar jobs with this employerAccentureVancouver, BC- $33.39–$57.43 an hour
- Full-time
- Provide Domain-Expertise on complex projects.
- Participate in requirements gathering and specifications creation.
- Participate in the Business process design.
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Job Post Details
Regulatory Affairs Associate - job post
Job details
Pay
- $46,563.40–$60,000.00 a year
Job type
- Full-time
Location
Full job description
The Regulatory Affairs Associate works in a cross-functional project environment to support assessment of products against regulatory frameworks and registration of products in North America.
Primary Responsibilities
· Compiles regulatory applications (primarily for Health Canada and the FDA) to achieve departmental and organizational objectives.
· Prepares regulatory documentation as appropriate in accordance with product classification and associated regulatory pathways (e.g., OTC/Pharmaceutical Drugs, Food Ingredients, Natural Health Products (NHPs)/Dietary Supplements, Veterinary Health Products, Cosmetics, Medical Devices).
· Supports literature reviews and drafting of safety and efficacy data.
· Supports reviews of product and manufacturing changes for compliance with applicable regulations.
· Keeps abreast of domestic and global regulatory trends, laws, and movements
Core Competencies
· Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements, prescription and non-prescription drugs, biologics, and medical devices preferred;
· Excellent oral and written communication, including technical writing skills and the ability to review and critique regulatory documents
· Ability to work well within a team and as an individual contributor.
· Computer literacy with MS Office Suite
Qualifications
· Bachelor’s Degree in a scientific discipline
· Minimum of 1-2 years industry experience, within the regulatory affairs function of a CRO/CPG/Pharmaceutical/Nutraceutical/Medical Device company
Pay: $46,563.40-$60,000.00 per year
Work Location: In person