Assignment Description

Our client is currently seeking a Consent Content Manager. As a Content Manager, you will work in a dynamic and agile cross-functional team to support the deployment of their Digital Health Products, including web portals, mobile applications, and devices. The position is available in either Barcelona or Mölndal.

Responsibilities:

• Manage product and study content throughout various stages of development and implementation as part of the Content Management Team.
• Advise on, design, and implement CMS architecture for project kick-off.
• Play a key role in the eConsent development squad, supporting content feature definition, design, development, and modeling.
• Coordinate content management activities during elaboration and feature development according to the product release plan and any study-related deadlines.
• Collaborate with Content Managers for other products to ensure efficiencies and continuity across products, including Unify product study onboarding activities and translation processes/requirements.
• Own and implement the end-to-end process for content management (processing, translation, and publication) for certain products.
• Work closely with the content director, content managers, and content editors to lead, plan, assess, resource, reuse, store, process, and manage content.
• Support product and clinical study teams during the maintenance and closeout phases with content change requests and bug fixing.
• Actively contribute to improvement initiatives and provide feedback within the digital health solutions.
• Thrive in a fast-paced, agile framework, speak up during wider cross-functional meetings, and maintain a fun, team-oriented atmosphere.

Required Qualifications:

• Bachelor’s Honors Degree in Communication, Media Information, Science and Health, or a related field.
• At least 5 years of hands-on experience as a Content Manager for digital products or solutions.
• Extensive experience with cloud-based or headless Content Management Systems (CMS) and Digital Asset Management systems (DAM).
• In-depth knowledge of the content production lifecycle within highly regulated science-based industries.
• Understanding of feature development lifecycle, agile ways of working (WoWs), and PI planning.
• Basic knowledge of web publishing, HTML, and desirable knowledge of SEO, JavaScript, and CSS.
• Ability to work collaboratively in a cross-functional setting with internal and external partners.
• Excellent stakeholder management and problem-solving skills, capable of managing deadlines under pressure.
• Exceptional communication skills, both written and verbal, with the ability to create clarity out of ambiguity.
• Meticulous proofreading and editing skills, with strong attention to detail.

Desired Qualifications:

• Familiarity with the clinical trial delivery or pharmaceutical landscape.
• Experience with Jira, Miro, and Figma.
• Experience working with headless CMS.
• Willingness to work globally, including international travel.
• Digital Project Management experience.
• Experience in a highly regulated environment with strict processes.
• Strong passion for health or working within the Life Science industry.