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Medical Device Upstream Marketing Jobs in Raleigh, NC

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · On-site

$40 - $42/hr

Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - ... Post Marketing Adverse Event Processing * Clinical Study SAE Processing * On Time Submission of AE ...

Baxter

Mgr, Global Product Marketing

Raleigh, NC · On-site

$149K/yr

... medical device, diagnostics or capital equipment), preferably with at least 1-2 of those years in an upstream or global capacity * Product life cycle management with knowledge of marketing strategies ...

Superbeo

Marketing Coordinator

Raleigh, NC · On-site

Marketing Coordinator Job Location: Raleigh, NC 27604 Job Duration: 6 months * Support and manage ... Minimum 1-2 years' experience in pharmaceutical, medical device, or skincare/beauty industry is ...

Superbeo

Brand Marketing Team Coordinator

Raleigh, NC · On-site

Brand Marketing Team Coordinator Job Location: Raleigh, NC 27604 Job Duration: 6 months Job Summary ... Minimum 1-2 years' experience in pharmaceutical, medical device, or skincare/beauty industry is a ...

Hearst

Product Marketing Manager

Durham, NC

$145K/yr

... medical device data into knowledge used by thousands of hospitals; the majority of U.S. health ... This is a strategic contributor responsible for the marketing success of some of FDB's most ...

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Medical Device Upstream Marketing information

See Raleigh, NC salary details

$21.4K

$46.1K

$71.9K

How much do medical device upstream marketing jobs pay per year?

As of Aug 30, 2026, the average yearly pay for medical device upstream marketing in Raleigh, NC is $46,146.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,900.00 and $52,000.00 per year, depending on experience, location, and employer.

What is a medical device upstream marketing?

A Medical Device Upstream Marketing job focuses on the early stages of product development, including market research, customer needs assessment, and product strategy. Professionals in this role work closely with R&D, regulatory, and commercial teams to define product requirements and ensure market fit. They analyze trends, gather customer feedback, and develop business cases to guide product development decisions. The goal is to create innovative medical devices that meet clinical and market demands while ensuring long-term commercial success.

What are the typical responsibilities of a medical device upstream marketing professional?

Professionals in Medical Device Upstream Marketing are primarily involved in market analysis, identifying customer needs, and helping define product requirements early in the development process. They collaborate closely with research and development teams, regulatory affairs, and sometimes directly with healthcare professionals to gather insights and refine product concepts. A significant part of the job includes building business cases, supporting innovation pipelines, and ensuring that new products have a strategically sound market fit. These tasks often require balancing technical information with commercial strategy and working within a cross-functional team environment.

What are the key skills and qualifications needed to thrive in medical device upstream marketing?

To thrive in Medical Device Upstream Marketing, you need strong analytical skills, a solid understanding of clinical and market trends, and experience with product development—often supported by a degree in marketing, engineering, or a related life sciences field. Familiarity with CRM software, market research tools, and regulatory compliance systems is typically required, and certifications in product management or medical device regulations can be advantageous. Strategic thinking, cross-functional collaboration, and clear communication are standout soft skills for this role. These competencies help ensure successful product strategy, alignment with unmet clinical needs, and effective coordination across internal and external stakeholders.

What are popular job titles related to Medical Device Upstream Marketing jobs in Raleigh, NC?

For Medical Device Upstream Marketing jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Medical Device Upstream Marketing jobs in Raleigh, NC are:

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Medical Device Upstream Marketing jobs near you

Medical Device Vigilance professionals

AA2IT

Raleigh, NC • On-site

$40 - $42/hr

Other

Posted 18 days ago

Job description

Medical Device Vigilance Professionals

Location: Raleigh, NC

Pay Rate: $40-42/HR on W2

Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.

Responsible for all tasks related to the collection, processing, follow up and regulatory reporting of adverse events (AEs), serious AEs from clinical trials (SAEs), adverse events of interest (AEIs) and pregnancy reports for all of Merz Aesthetics marketed and investigational products.

This position will routinely process all types of reports for all categories of products (medical device, cosmetic and OTC products).

Major Duties Description:

  • Post Marketing Adverse Event Processing
  • Clinical Study SAE Processing
  • On Time Submission of AE Reports
  • Evaluation of Individual AE Reports and Safety Data
  • Literature Reviews
  • Safety Database Proficiency
  • Review and Update of Departmental Documents
  • Provides Training Regarding AE Reporting
  • Audit Support
  • Supports Regional Safety/Vigilance
  • Collaborate with Other Global Functions

Technical & Functional Skills:

  • Thorough knowledge and experience in all aspects of safety reporting for clinical trials and marketed products – both drugs and medical devices.
  • Strong knowledge and experience with validated safety databases (Argus, ARISg, SIAB, etc.). This also includes MedDRA, WHODrug, and IMDRF coding.
  • Must work effectively/collaboratively in a fast-paced yet efficient team environment with individuals at all levels within an organization.
  • Strong knowledge of FDA and EU regulations governing clinical safety and vigilance.
  • Strong organizational and project management skills.
  • Strong verbal and written communication skills.

Minimum Qualifications:

  • Bachelor's degree in a science or health care-related field or RN/PharmD
  • 5+ years of experience in drug safety or medical device vigilance (preferred) in an industry setting or equivalent

Preferred Qualifications:

  • Direct health care experience with injectable products highly desired
  • Knowledge and experience with document management systems (EDMS, eTMF, etc.)
  • Experience in vendor management
  • Demonstrates relationship building and problem-solving skills

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