Oakville, On Marketing strategist Jobs – 17 Openings This Week

Regulatory Data and Content Professional (Senior Medical Writer)
Integrated Resources - Hosted Jobs —Mississauga, ON
- $56.73–$63.82 an hour
- Contract
- Google Suite
- English
- Microsoft Office
Quick apply
2d
Client Success Manager - Digital & Performance Marketing
Measure Marketing Results Inc. —Oakville, ON
- Full-time
- English
- Analysis skills
- Budgeting
- Dental care
Quick apply
Content Strategist
HP —Mississauga, ON
- $86,350–$127,800 a year
- Full-time
- Sales
- Writing skills
- Project management
- Disability insurance
- Dental care
Sr. Industry Marketing Strategist
OpenText —Mississauga, ON
- $118,000–$168,000 a year
- Sales
- Public speaking
- Presentation skills
- Paid time off
Marketing Operations Manager
Konrad —Toronto, ON
- $95,000–$125,000 a year
- Hybrid work
- SQL
- APIs
- Communication skills
- Work from home
- Flexible schedule
Quick apply
4d
Stratège de produit - Engagement numérique/ Product Strategist - Digital Engagement
IQVIA —Mississauga, ON
- $95,800–$145,800 a year
- Full-time
- Hybrid work
- Sales
- Master's degree
- Bachelor's
Commercial Strategy Manager
Greenstone Meats —Etobicoke, ON
- $115,000–$130,000 a year
- Sales
- Marketing
- Research
- Disability insurance
- Dental care
Quick apply
3d
Martech Specialist
Konrad —Toronto, ON
- $65,000–$80,000 a year
- Hybrid work
- SQL
- Analysis skills
- APIs
- Work from home
- Flexible schedule
Quick apply
4d
Senior Adobe Martech Specialist
Konrad —Toronto, ON
- $85,000–$105,000 a year
- Hybrid work
- Organizational skills
- APIs
- Communication skills
- Work from home
- Flexible schedule
Quick apply
4d
VP, Brand Strategy
BGBx —Mississauga, ON
- $200,000–$240,000 a year
- Remote
- Presentation skills
- Communication skills
- Paid time off
- Life insurance
Quick apply
MarTech Developer
Konrad —Toronto, ON
- $90,000–$120,000 a year
- Hybrid work
- Java
- SQL
- Analysis skills
Quick apply
Intermediate Digital Designer
Harbinger Communications —Toronto, ON
- Full-time
- Hybrid work
- HTML
- Time management
Quick apply
AI Marketing & Community Lead
Product Faculty —Mississauga, ON
- $85,000–$100,000 a year
- Full-time
- In-person
Quick apply
2d
Regulatory Data and Content Professional (Senior Medical Writer)
Amaris Consulting —Mississauga, ON
- $90,000 a year
- Temporary
- Google Suite
- No experience needed
- English
2d
Director, Strategy
Diamond —Toronto, ON
- Full-time
- Hybrid work
- Presentation skills
- Marketing
Quick apply
7d
Content Marketing Strategist - Digital Marketing Agency
Blue Ocean Interactive Marketing —Canada
- $65,000–$75,000 a year
- Full-time
- Remote
- Writing skills
- English
- Project management
- Dental care
- Paid time off
Quick apply
14h

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marketing strategist jobs near oakville, on

Regulatory Data and Content Professional (Senior Medical Writer)

Integrated Resources - Hosted Jobs -
Mississauga, ON

Quick apply

Job details

Contract
$56.73–$63.82 an hour
2 days ago

Qualifications

Google Suite
Project planning
English
Microsoft Office
Content development
Content strategy
Communication skills
Adobe Acrobat

Full job description

Title: Regulatory Data and Content Professional (Senior Medical Writer)
Location: Mississauga, ON Hybrid Role
Duration: 12 months+
Pay: $ 56.73-$ 63.82/hr. on T4

Work Location: This is an onsite role. Selected candidates will be required to work at the Mississauga Campus 3 days every week.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.

That’s what makes us Client.

The Pharma Development Regulatory (PDR) is a flexible, Product, and distinctive regulatory organization. We make decisions quickly and strategically as the environment & landscape evolves.
We innovate. Within the PDR Data and Content Chapter, we are responsible for end-to-end data interpretation, generation and execution of content strategy, insight generation to guide submission strategy, and leadership of submission planning and management for clinical projects in the Client portfolio in order to develop and maintain Client product permits/licenses to meet the needs of our patients.
We understand how data and information contribute to the strategy and quality of submissions, and thus, deliver high-quality submissions to global Health Authorities for products throughout their development lifecycle to facilitate reviews and approvals.
We ensure audit and inspection readiness and representation. Additionally, as a member of PDR, individuals understand how data and information contribute to the quality of our submissions
As a member of this Chapter, you will drive and manage data interpretation and content, including medical writing, from initiation to approval, developing data and content standards, driving and articulating key messages, content creation, strategic reuse of content, and implementing automation and next-generation systems and tools.

The Opportunity:

Leads a team of Content Strategists and/or cross-functional teams in development and execution of the content strategy for submission to global regulatory authorities in accordance with applicable regulatory guidelines/Client standards/SOPs. Regulatory content may include the Clinical Dossier and/or Suite of Safety reports for drugs or medical devices
Plans content and create timelines for the production and review of documents, ensuring alignment with overall project timelines where appropriate.
Reviews documents for organization, clarity, scientific standards, and consistency of content, data, and messaging.
Resolves issues with cross-functional contributors. Ensures compliance with regulatory requirements and internal processes
Is a key strategic participant in functional and cross functional teams and actively contributes to best practices and continuous improvement initiatives and projects
Partnering with key stakeholders, working on the molecule portfolio, or continuing to key initiatives that shape our technical, business and healthcare environments.
Maintains up-to-date knowledge of key regulatory, scientific, and medical topics relevant to drug development and disease/therapeutic areas
May act as a mentor to new or less experienced Content Strategists

Who you are:

Degree in Life Sciences or equivalent with 5 years of relevant experience in the pharmaceutical/biotechnology industry, demonstrating independent project delivery and leadership. Experience in leading cross-functional teams.
Familiar with regional/global drug and device development processes, regulations, and guidelines (e.g., GxP, GCP, ICH, ISO, and MDR/IVDR) and an understanding of GVP and GCP principles, including data integrity.
Demonstrated expertise in clinical, safety and/or device regulatory documentation throughout the product lifecycle, from early development through post-marketing activities.
Ability to independently analyze and synthesize data and non-clinical and clinical concepts from a broad range of disciplines.
Proven ability to drive outcomes in global filings (strongly preferred) and other regulatory projects by collaborating across diverse, cross-functional teams, leveraging strong communication and interpersonal skills to build trust, foster collaboration, and resolve conflicts in matrixed environments.
Excellent administrative and project planning skills, with proficiency in G Suite, Microsoft Office Suite, Adobe Acrobat, and Veeva Vault; detail-oriented, creative thinker with a curiosity to learn and adapt to change, and fluent in English (verbal and written).

Mandatory Skills Required:

Degree in Life Sciences or equivalent
5 years of relevant experience in the pharmaceutical/biotechnology industry, demonstrating independent project delivery and leadership. Experience in leading cross-functional teams.
Familiar with regional/global drug and device development processes, regulations, and guidelines (e.g., GxP, GCP, ICH, ISO, and MDR/IVDR) and an understanding of GVP and GCP principles, including data integrity.
Demonstrated expertise in clinical, safety and/or device regulatory documentation.

Top Primary Goals:

Get onboarded quickly to Client internal document development processes and relevant SOPs.
Prepare for and kick off the cross-functional authoring process for an assigned project.

#IRI-BP

Pay: $56.73-$63.82 per hour

Work Location: Hybrid remote in Mississauga, ON L5N 5M8

Quick apply

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marketing strategist jobs in oakville, on

Regulatory Data and Content Professional (Senior Medical Writer)

Client Success Manager - Digital & Performance Marketing

Content Strategist

Sr. Industry Marketing Strategist

Marketing Operations Manager

Stratège de produit - Engagement numérique/ Product Strategist - Digital Engagement

Commercial Strategy Manager

Martech Specialist

Senior Adobe Martech Specialist

VP, Brand Strategy

MarTech Developer

Intermediate Digital Designer

AI Marketing & Community Lead

Regulatory Data and Content Professional (Senior Medical Writer)

Director, Strategy

Content Marketing Strategist - Digital Marketing Agency

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