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Health Research jobs in Calgary, AB

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    • Medical Devices (Class I–II).
    • Natural Health Products (NHPs/NPNs).
    • The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures…
    • Ability to conduct research into software development and delivery concepts, as well as technical application issues.
    • Highly self motivated and directed.
    • Support collaboration with external partners, research institutions, and industrial stakeholders in the mining, metals, and recycling sectors.
    • Talent Acquisition: Lead the hiring and onboarding of new research staff to support company scaling.
    • Leadership: Proven track record of managing teams and "…
    • Exposure to innovative clinical research and emerging therapies.
    • Build and maintain relationships with sponsors, CROs, and research partners.
    • Elicit, analyze, document and validate business requirements using a variety of tools including research, interviews, document analysis, and process analysis.
    • BMO also offers health insurance, tuition reimbursement, accident and life insurance, and retirement savings plans.
    • An understanding of and interest in undertaking action research.
    • Understanding of teacher competencies and growth within the Teaching Quality.
    • Strong research and investigative skills.
    • Oversee and make recommendations for health & safety programs, policies and procedures.
    • We are seeking an experienced R&D Lead in Organometallic Chemistry or Hydrometallurgy to lead research programs focused on the recovery of valuable metals from…
    • Candidate would be a liaison between Operations teams and Invoicing teams.
    • Auditing completed orders to ensure all job costs / expenses are captured, potential…
    • Conduct basic compliance research on evolving AESO and NERC requirements.
    • Relocation assistance will be provided.
    • Nice to Have (Not Required).
    • Ability to conduct research and create reports or presentations.
    • The chance to make a meaningful impact on the health and safety of our teams across Canada.
    • We offer a competitive salary, excellent benefits, including paid parental leave, family sick time, and health insurance—and a fulfilling work environment where…
    • We are seeking a permanent full-time Product Safety Advisor with a focus on North American Chemical Control Regulations.
    • Must work well in a team setting.
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Job Post Details

Pharmaceutical Regulatory Affairs Specialist - job post

CRL Synergy
Calgary, AB T2S 1W3
$68,000–$100,000 a year - Full-time

Job details

Pay

  • $68,000–$100,000 a year

Job type

  • Full-time

Location

Calgary, AB T2S 1W3

Benefits

Pulled from the full job description

  • Paid time off
  • Vision care
  • Dental care
  • Life insurance
  • Disability insurance
  • On-site gym
  • Extended health care

Full job description

Job Overview
CRL Synergy, one of Canada’s largest and fastest-growing suppliers of control label products, is seeking a detail-oriented and proactive Regulatory Affairs (RAS) Specialist.CRL Synergy is seeking a Regulatory Affairs (RAS) Specialist who can thrive in a fast-paced environment that involves working in an office team environment.

The Regulatory Affairs Specialist is the site lead for all Health Canada submissions and post-market activities covering four product categories sold across Canada:

  • Drugs (DIN-assigned OTC)
  • Cosmetics
  • Medical Devices (Class I–II)
  • Natural Health Products (NHPs/NPNs)

The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures compliant labelling/advertising.

This role will also provide quality assurance support through maintenance of the RA SOPs, ensuring they are current and implemented, perform data collection, and subsequent analysis.

The successful candidate will provide support for new product development, ensuring Health Canada and customer requirements are being met, including labelling accuracy for new and modified product.

Responsibilities

  • Oversight of Pharmacovigilance program

· Collaborate with cross-functional teams to implement corrective and preventive actions (CAPA) related to customer complaints.

· Participate in risk management activities and contribute to the development of risk assessment strategies.

  • Ensuring accurate record keeping and filing as per organizational procedures.
  • Handle clerical and administrative activities.
  • Review and assess customer complaints for adverse reactions and reportable incidents. Perform surveillance activities for ongoing product quality and safety.
  • Complete Annual Summary Reports and perform screening of scientific literature for product safety information.
  • Assisting in updating methods and procedures (SOPs) related to the Quality Management System with a focus on the customer complaint and pharmacovigilance program.

Qualifications

  • Bachelor’s degree in a relevant field; advanced degree preferred.
  • Proven experience in regulatory affairs or a related field, with a strong understanding of compliance requirements.
  • Demonstrated skills in project management, including the ability to manage multiple projects simultaneously.
  • Strong leadership abilities with experience in supervising teams or mentoring staff.
  • Excellent analytical skills with a focus on process improvement methodologies.
  • Familiarity with sales or business development processes is a plus.
  • Exceptional communication skills, both written and verbal, with the ability to effectively convey complex information to diverse audiences. Join us in making a difference through compliance excellence!

Job Type: Full-time

Pay: $68,000.00-$100,000.00 per year

Benefits:

  • Company events
  • Dental care
  • Disability insurance
  • Extended health care
  • Life insurance
  • On-site gym
  • On-site parking
  • Paid time off
  • Vision care

Education:

  • Bachelor's Degree (preferred)

Experience:

  • Regulatory Affairs: 2 years (preferred)

Work Location: In person

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