Medical Affairs jobs in Ontario
- Jazz PharmaceuticalsMississauga, ON
- $180,000–$270,000 a year
- Dental care
- Life insurance
- Disability insurance
- Paid vacation
- Extended health care
- RRSP
- The Director, Regulatory Affairs, Canada, is a member of the Global Regulatory Affairs and Drug Safety (GRADS) team and is responsible for providing strategic…
- NovartisToronto, ON
- $121,873–$169,188 a year
- Full-time
- As an Health Economics Manager, you will play a critical role in driving successful health technology assessment (HTA) submissions and ensuring timely access to…
Research Manager
Easily applyNewConfidentialOakville, ON- $70,000–$95,000 a year
- Full-time
- Set annual research goals in alignment with organizational strategy and develop a budget plan for approval, ensuring all research projects have clear objectives…
- Wellington-Dufferin-Guelph Public HealthGuelph, ON
- $70.53–$163,395.58 an hour
- Full-time +1
- Monday to Friday +1
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Life insurance
- Employee assistance program
- Critical thinking, ability to analyze complex technical and medical information.
- Depending on the role and operational needs, flexible or hybrid work…
- Wellington-Dufferin-Guelph Public HealthGuelph, ON
- $70.53–$163,395.58 an hour
- Full-time +1
- Monday to Friday +1
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Life insurance
- Employee assistance program
- Critical thinking, ability to analyze complex technical and medical information.
- Depending on the role and operational needs, flexible or hybrid work…
Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $46,563.40–$60,000.00 a year
- Full-time
- Minimum of 1-2 years industry experience, within the regulatory affairs function of a CRO/CPG/Pharmaceutical/Nutraceutical/Medical Device company.
- NovartisToronto, ON
- Full-time
- Strong experience engaging with HCPs/Medical Experts and leading field medical teams.
- Oversee MSL strategy and ensure aligned field medical engagement and…
- Niagara RegionThorold, ON
- $91,180–$107,260 a year
- Full-time +1
- Dental care
- Employee assistance program
- Health Promotion and Foundational Standards.
- As an employer of choice, Niagara Region offers competitive salaries and benefits, a defined benefit pension plan,…
President and CEO
Easily applyEvo Radiologic Consultants Inc.Toronto, ON M5V 1V6- From $52.63 an hour
- Full-time
- 40 hours per week
- Monday to Friday +1
- Paid time off
- Dental care
- Extended health care
- Flexible schedule
- Management experience in the medical field.
- Thorough mastery of up-to-date techniques and services in the practice of radiology with knowledge of how to…
- Philip Morris InternationalOttawa, ON
- From $215,600 a year
- Full-time
- 8–12+ years of experience in government relations, regulatory affairs, or public policy.
- Build and manage relationships with key political stakeholders,…
Senior Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $60,000–$90,000 a year
- Full-time
- Interacts with internal and external groups to provide regulatory affairs consultative support for projects.
- Initiates and manages regulatory affairs projects…
View similar jobs with this employer26-017 Clinical Director, Client and Participant Services
Easily applyNewSickKids CCMHToronto, ON M4Y 2H4- $129,300–$140,250 a year
- Full-time +1
- On call
- Paid time off
- Life insurance
- Employee assistance program
- Disability insurance
- Company pension
- Extended health care
- POSITION DETAILS: Regular, 1.0 FTE, 35 hours/week *.
- GH-CCMH is also a member of the Thriving Minds Mental Health Access Collaborative with CAMH and SickKids…
Theraputic Area Lead, Critical Care
Easily applyNewOctapharma CanadaToronto, ON- Full-time
- You are expected to understand the clinical evidence as deeply as any medical affairs professional and to translate that depth into commercial plans that…
Excellence in Team-Based Care Project Manager
Easily applyThe College of Family Physicians of CanadaMississauga, ON L4W 5A4- $94,437.84–$118,046.88 a year
- Full-time +1
- Monday to Friday
- The College establishes the standards for and accredits postgraduate family medicine training in Canada’s 17 medical schools.
- Term of Contract: 2 Years*.
Regulatory Affairs Specialist
Easily applyNewAdecco CanadaOttawa, ON- $85,000–$90,000 a year
- Contract +1
- Monday to Friday
- Dental care
- In this role, you will work closely with cross-functional teams to manage regulatory submissions, support product development initiatives, maintain compliance…
- FitziiMississauga, ON
- Full-time
- Reporting to the Director of Sales the Regional Sales Manager will be responsible for driving regional sales performance, executing national strategies, and…
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Job Post Details
Director, Regulatory Affairs Canada - job post
Job details
Pay
- $180,000–$270,000 a year
Location
Benefits
Pulled from the full job description
- Dental care
- Life insurance
- Disability insurance
- Paid vacation
- Extended health care
- RRSP
Full job description
The Director, Regulatory Affairs, Canada, is a member of the Global Regulatory Affairs and Drug Safety (GRADS) team and is responsible for providing strategic regulatory direction for designated projects, ensuring that the latest Health Canada requirements and standards are met. The individual will interface with Health Canada and business partners regarding development, regulatory and registration strategies. With a solid reporting line into Global Regulatory Affairs (Regulatory Strategy), the individual will also be a member of the extended Canadian leadership team.
Principal Duties and Responsibilities:
Canadian Regulatory Lead - Function as a leader in Jazz GRADS and Canada’s extended leadership team and serve as Regulatory Responsible Person.
Act as local regulatory point of contact for the product collaborating with Global Regulatory Lead (GRL) / Global Regulatory Team (GRT):
- Provides, as subject matter expert, strategic and operational regulatory input (including Health Authority Insights) on projects including, but not limited to, Canadian regulatory strategies, regulatory requirements for clinical studies, marketing approval and post-approval activities in Canada, regulatory strategic development plans and risk assessments, critical issue management and advice on Regulatory Interactions with Health Canada.
- In partnership with the Global Regulatory Lead (GRL) and other technical experts, liaises and negotiates with Health Canada, as needed, pertaining to drug development including resolution of key regulatory issues and to expedite product approvals and labelling, with clear documentation of discussion and agreements, as directed by line management.
- Maintains awareness of the global regulatory environment and assesses the impact of changes on business and product development programs.
- Builds partnerships with key peers and senior stakeholders from other functions to ensure that strategic business goals are met through the sharing of knowledge, expertise, and the provision of appropriate resources.
- Responsible for assisting with the development, implementation and enforcement of regulatory processes.
- Support global regulatory in product submissions, market authorization, and label updates in collaboration with Regulatory Strategy, Global Product Labelling and INSPIRE teams, as applicable
- Support product expansion activities in international markets, such as Middle East, North Africa, Latin America and Asia Pacific markets, as applicable.
- Support Health Canada inspections as Regulatory Strategy point person
Required Knowledge, Skills, and Abilities
- Previous experience of Responsible Person responsibilities in a corporate setting.
- Previous experience of undertaking regulatory submissions, ideally in a corporate pharmaceutical environment.
- Progressive experience within the pharmaceutical industry including Regulatory Affairs.
- Deep knowledge of business and market dynamics.
- Strong knowledge of the local legislation in the pharmaceutical market as well as of SOPs, policies and procedures.
- Thorough understanding of drug development processes and the pharmaceutical industry and healthcare environment including regulatory requirements and policy trends.
- Regulatory experience with CTAs, NDSs, lifecycle management, interactions with Regulatory Agencies, and developing and implementing regulatory strategies with a proven track record of significant regulatory accomplishments.
- Able to understand and optimize internal processes.
- Technical competencies on regulatory and governance linked to the Canadian market and organization
- Proven interpersonal skills with the ability to work collaboratively and flexibly as a member of a cross-functional team. Ability to establish and maintain effective working relationships.
- Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism.
- Skilled in conflict resolution/negotiation. Fosters open communication. Listens and facilitates discussion.
- Problem solving; strong negotiating skills and ability to think creatively and develop creative solutions.
- Excellent command of English; excellent verbal and written skills. Able to analyze, define and effectively convey difficult and complex issues in a way that accurately and persuasively communicates the issues to internal and external stakeholders.
Required/Preferred Education and Licenses
- Bachelor’s degree: Masters or other advanced degree preferred.
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Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
FOR CANADA BASED CANDIDATES ONLY
Jazz Pharmaceuticals Canada, Inc. and Celator Pharmaceuticals Corp. are committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive.
For this role, the full and complete base pay range is: $180,000.00 - $270,000.00
Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual pay decisions. This range will be reviewed on a regular basis.
At Jazz/Celator, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz’s Long Term Equity Incentive Plan.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, Extended Health Care, Dental, Long Term Disability, Life Insurance, RRSP, and paid vacation.