Referso Jobs

Senior Director, Marketing Capabilities and Operations

Innoviva Specialty Therapeutics · Posted Nov 7, 2026

Open

Waltham, Massachusetts, United States
Senior
10+ years

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Senior Director, Marketing Capabilities and Operations

Innoviva Specialty Therapeutics · Posted Nov 7, 2026

Open

Waltham, Massachusetts, United States
Senior
10+ years

Apply with Referso

Regulatory Affairs Manager SASSA

Elanco · Posted Nov 6, 2026

Open

Centurion, Gauteng, South Africa
On-site

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Support the maintenance of existing and registration of new animal health products, including therapeutics, feed additives, biocides and care products.

Responsibilities

Manage regulatory compliance and lifecycle activities for the existing and future portfolio, including submissions, variations, renewals and referrals to the South African Health Products Regulatory Authority and other relevant authorities.
Develop and implement regulatory strategies for export markets across the region, while building effective relationships with competent authorities and external regulatory partners.
Coordinate packaging development and artwork activities, including the release of production artwork through the Elanco Artwork System.
Review and approve promotional materials in PromoMats, and coordinate national regulatory issues, submissions and packaging updates.
Maintain regulatory information in systems such as Veeva Vault RIM, collaborate with internal and external stakeholders, and lead regional Regulatory Affairs projects as required.

Requirements

Pharmacist qualification
Nice to have: similar experience from the animal health industry
Nice to have: fluent English

Skills

regulatory compliance activities submissions

Analyst - Medical Information

AstraZeneca · Posted Nov 6, 2026

Open

Bangalore, India

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Analyst responsible for creating, reviewing, and maintaining high‑quality medical content for US‑marketed products, ensuring scientific accuracy and compliance while leveraging digital tools and AI.

Responsibilities

Develop, review, update and maintain medical content across formats
Deliver accurate responses to Medical Information Requests for US products
Design literature searches and custom responses for advanced inquiries
Use medical information and content management systems (GMIP Inquiry, Vault MedComms, PromoMats, AIMI)
Conduct medical accuracy checks, quality assurance, editorial and promotional reviews

Requirements

Advanced scientific degree (PharmD preferred, MD, PhD, or equivalent)
Nice to have: Digital content development
Nice to have: Digital content strategy
Nice to have: Mentoring and coaching
Nice to have: Proficiency with GMIP Inquiry, Vault MedComms, PromoMats, AIMI

Skills

Medical information Scientific communications Clinical and healthcare systems expertise Scientific/medical writing Content creation (e.g., slide decks)Strategic problem solving Project management Organizational skills Technology/platform proficiency Collaboration across teams Regulatory, legal and compliance knowledge GMIP Inquiry Vault MedComms

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Analyst - Medical Information

AstraZeneca · Posted Nov 6, 2026

Open

Bangalore, Karnataka, India
On-site
Full-time

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Responsible for creating, reviewing, and maintaining high-quality medical content for US products, ensuring scientific integrity and compliance across multiple formats.

Responsibilities

Develop, review, update and maintain medical content across formats
Deliver accurate answers to Medical Information Requests for US products
Design literature searches and custom responses for advanced inquiries
Use medical information and content management systems to streamline creation and reporting
Perform literature searches and evaluate evidence quality

Requirements

Advanced scientific degree (PharmD preferred, MD, PhD, or equivalent)
Nice to have: Experience developing digital content
Nice to have: Mentoring and coaching
Nice to have: Familiarity with US medical information processes

Skills

Medical information Scientific communications Content creation Literature searches Regulatory compliance

Manager, Commercial Technology & Digital Solutions

Arrowhead Pharmaceuticals · Posted Nov 5, 2026

Open

Pasadena, California, United States
On-site
Full-time · Manager
$120K–$150K per year
5+ years

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The Manager, Commercial Technology, is a hands‑on role responsible for the daily operation of commercial platforms, reporting, marketing technology, and brand websites.

Compensation

California pay range $120,000—$150,000 USD

Responsibilities

Build, update, and troubleshoot Power BI dashboards and reports for commercial teams and leadership.
Use Databricks SQL and notebooks to query, transform, and validate commercial data and maintain reporting tables and views in coordination with Enterprise Data Management.
Monitor scheduled data workflows, investigate refresh failures and data discrepancies, and coordinate fixes with Enterprise Data Management, data engineering teams, and vendors.
Support connections between Databricks and Power BI, including data availability, refresh schedules, access, and troubleshooting.
Partner with Enterprise Data Management to configure and maintain Databricks Genie for commercial use cases, including selecting datasets, documenting business terminology and metric definitions, and providing instructions and example SQL queries.

Requirements

Bachelor’s degree in Computer Science, Information Systems, Life Sciences, Engineering, Business, or a related field.
Nice to have: Databricks Unity Catalog
Nice to have: Python
Nice to have: APIs
Nice to have: HTML/CSS

Senior Account Manager

Klick · Posted Nov 4, 2026

Open

London, England, United Kingdom
Hybrid
Full-time · Senior
5+ years

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Supports client relationships and day-to-day delivery across healthcare and life sciences accounts in the UK, partnering with cross-functional teams to ensure project success.

Responsibilities

Manage day-to-day client communications, status meetings, actions, and follow-ups across healthcare or pharmaceutical account work.
Coordinate cross-functional delivery with Strategy, Creative, Medical, Project Management, and Production teams to keep projects on brief, on time, and on scope.
Support scopes, estimates, timelines, budgets, and change requests in partnership with Project Management and account leadership.
Prepare client-facing materials, meeting agendas, contact reports, status updates, and project documentation with clear next steps.
Track project risks, feedback, approvals, and regulatory review requirements to support compliant, high-quality delivery.

Requirements

Nice to have: AI usage
Nice to have: UK, EMEA, or multi-market healthcare account experience
Nice to have: Veeva
Nice to have: Zinc
Nice to have: PromoMats

Skills

client service experience in an advertising/marketing agency pharmaceutical, healthcare or life sciences experience

Senior Medical Copywriter

Enero · Posted Nov 5, 2026

Open

Sydney, New South Wales, Australia
Senior
5+ years

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Senior Medical Copywriter

Responsibilities

Translate complex medical/scientific concepts into clear, concise copy
Create branded HCP campaign materials including websites, detail aids, leave behinds, emails
Create HCP medical education campaign materials including slide decks, invites, workbooks, and other collateral
Lead brands from both strategy and copy perspectives with minimal oversight
Drive the editorial process from first draft to final proof; ensure accuracy and quality

Requirements

Graduate degree or PhD in sciences discipline

Skills

medical writing experience HCP pharmaceutical advertising agency experience claim development and substantiation presentation and pitching experience knowledge of Medicines Australia Code of Conduct proficiency with Veeva/PromoMats

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