Full-Time

Labeling Artwork Controller Consultant

ClinChoice

ClinChoice

1,001-5,000 employees

Global CRO providing full-service clinical development

No salary listed

Remote in Italy

Remote

Bachelor's

Category
Operations & Logistics
Manufacturing Quality & Test (1)
Required Skills
Adobe InDesign
Veeva
Agile
Six Sigma
Adobe Photoshop
Adobe Illustrator

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Requirements
  • Bachelor’s degree in Life Sciences, Business, Packaging Technology, or related field
  • 10+ years in labeling design, proofreading, coordination, regulatory, packaging, and project management within consumer health, pharmaceutical, or medical device industries
  • Strong knowledge of global regulatory requirements for product labeling and packaging
  • Proven ability to manage multiple projects and cross-functional teams in a deadline-driven environment
  • Hands-on experience with product lifecycle management and electronic artwork systems (e.g., Agile, GLAMS, Loftware, Veraciti, Veeva)
  • Expertise in Adobe Creative Suite (Illustrator, InDesign, Photoshop, Acrobat Pro)
  • Familiarity with pre-press and print processes (CMYK, Pantone, dielines, bleed, etc.)
  • Skilled in proofreading tools (e.g., TVT, GlobalVision, InformCC) and regulatory content validation
  • Six Sigma Green Belt certification or equivalent experience in continuous improvement
  • Excellent communication, problem-solving, and organizational skills
Responsibilities
  • Manage the end-to-end artwork development process from initiation through approval and release, ensuring timely delivery of high-quality labeling components
  • Act as the primary liaison between PMO, Regulatory Affairs, Marketing, Packaging, Quality, Supply Chain, and external vendors/agencies
  • Validate briefs for accuracy and completeness; collaborate with cross-functional teams to resolve discrepancies
  • Oversee timelines, resource planning, and progress tracking for multiple concurrent labeling projects
  • Coordinate review and approval of labeling content and artwork in internal systems, ensuring compliance with regulatory, legal, and corporate standards
  • Drive process improvements related to artwork development, approval workflows, and digital tools
  • Investigate Root Cause Analyses (RCAs) and implement Corrective and Preventive Actions (CAPA) as needed
  • Maintain artwork issue logs and attend escalation meetings to provide updates
  • Identify inefficiencies and escalate to Hub Leads when required
  • Participate in content lock meetings to ensure stakeholder alignment
  • Manage Veraciti system-related issues and escalate appropriately
  • Suggest and implement technology solutions for artwork and labeling processes
  • Create, update, and maintain training documentation for systems and processes
  • Supervise Artwork Controllers to ensure task completion and provide support during peak periods
  • Onboard new hires on artwork management systems and end-to-end processes; conduct quarterly refreshers on best practices
  • Provide guidance on escalation channels and support SMEs, Artwork Process Leads, Vendors, and Hub Leads with artwork production deployment
  • Track and follow up on action items from cross-functional meetings
  • Communicate project status, risks, and milestones consistently to stakeholders
  • Attend regional project meetings (Kick-off, Overview, Alignment, Technical with Printer) and provide updates
  • Share project insights for dashboards and analytics; contribute to KPI reviews and compliance initiatives
  • Gather requirements for new regional jobs and assess resources requirements and provide job quotations when required
  • Conduct design-to-press color management assessments and feasibility consultations
  • Monitor and maintain regional project timelines and costs; anticipate and resolve roadblocks
  • Address process and executional quality issues; support system and process improvements
  • Manage ad-hoc artwork-related requests and cascade process/system communications
Desired Qualifications
  • PMP certification or formal project management training

ClinChoice provides outsourced clinical development services as a global CRO for pharmaceutical, biotechnology, medical device, and consumer health clients. It supports trials across the full lifecycle with services including clinical operations, biostatistics, data management, regulatory affairs, medical affairs, pharmacovigilance, and project management, and it offers project-based or Functional Service Provider (FSP) engagement models. The company differentiates itself through its scale and international reach (4,000+ professionals in 30+ countries) and a track record of 1,500+ full-service studies, aided by growth from mergers and acquisitions. Its goal is to help clients accelerate drug and device approvals by efficiently managing multinational trials and navigating complex regulatory environments throughout development and post-marketing.

Company Size

1,001-5,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Whitemarsh Township, Pennsylvania

Founded

1995

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Simplify Jobs

Simplify's Take

What believers are saying

  • Monash University partnered with ClinChoice on March 23, 2026 for early-phase trials.
  • Revelio Labs reported 2,339 employees in March 2026 and 133 active 2026 postings.
  • Legend Capital's 2022 $150 million round still funds expansion and acquisition capacity.

What critics are saying

  • Revelio Labs shows active postings fell 27.8% in 2026, signaling weaker demand.
  • ClinChoice's workforce slipped from 2,348 in 2023 to 2,339 in 2026.
  • A failed integration of CROMSOURCE, CSI, and Medidata systems would break delivery quality.

What makes ClinChoice unique

  • ClinChoice spans 30+ countries, enabling multinational trials across Asia, Europe, and North America.
  • Its 2023 CROMSOURCE and 2024 CSI acquisitions deepened full-service and Southeast Asia reach.
  • The 2024 Medidata extension adds Clinical Data Studio to its data-management stack.

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Benefits

Remote Work Options

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

7%

1 year growth

7%

2 year growth

7%
PR Newswire
Jan 12th, 2024
ClinChoice Acquires CSI, Expanding its Global Footprint into Southeast Asia

/PRNewswire/ -- ClinChoice, a leading global Contract Research Organization (CRO), today announced expanding its global footprint with the acquisition of CSI...

TalentSource Life Sciences
Mar 20th, 2023
Outsourcing in Clinical Trials Southeast 2023 – TalentSource Life Sciences

On March 1 st, 2023 ClinChoice acquired CROMSOURCE, strengthening its global network and deepening its full-service capabilities.

AVCJ
Jul 6th, 2022
Legend Capital invests into ClinChoice Inc. in $150M

US and China-based clinical contract research organization (CRO) company ClinChoice has raised a USD 150m Series E round led by Legend Capital.

Endpoints News
Jul 5th, 2022
Fountain Medical Development Ltd receives financing of $150M in Series E funding round

ClinChoice, formerly Fountain Medical Development, has completed a $150 million Series E funding round, using the cash to continue its planned expansion.

The HealthCo
Apr 13th, 2022
Cloudbyz, Inc. partnered with ClinChoice Inc. on Apr 13th 22'.

Cloudbyz, a fast-growing integrated clinical research and development solution provider with integrated capabilities, today announced a partnership with ClinChoice, a global full-service clinical CRO dedicated to offering high-quality one-stop service to biopharmaceutical, Vaccine, Medical Device, Cosmetics, Nutraceuticals, and Consumer Products clients.