Publications & Content Manager

Trust In SODA

Dublin

Hybrid

EUR 59,000 - 66,000

Part time

10 days ago
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Job summary

Trust In SODA is seeking a Content Project Manager for a 6-month contract in Dublin. Hybrid role with 2/3 days in the office, starting ASAP, offering €320–€360 per day PAYE.

You will oversee globally applicable publication plans and content programs across therapeutic areas, coordinating cross-functional teams and ensuring regulatory compliance throughout the lifecycle.

Qualifications

  • 2+ years of pharmaceutical industry or medical communications agency experience or post-university experience desirable
  • Advanced project management skills
  • Strong financial and business acumen
  • Experience in Medical Affairs/Medical Services leadership delivery roles or providing services to large pharmaceutical organization desirable
  • Experience of working in an international environment.
  • Exemplary interpersonal and listening skills
  • Ability to work with demanding professionals
  • Strong attention to detail
  • Team player
  • Flexible with difficult timelines
  • Advanced understanding of business processes
  • Track record of operational effectiveness or operational innovation.

Responsibilities

  • The remit of responsibilities centers on globally applicable content elements aligned to the SCP, delivered in adherence with guidelines and regulatory compliance.
  • Exceptional project management expertise and ability to influence outcomes in a highly matrixed environment.
  • Accountable for high-quality scientific publication plans and content programs across the portfolio asset lifecycle.
  • Operate as project management contact for assigned content programs and publication plans.
  • Collaborate with stakeholders to understand needs and deliver publications and content development plans.
  • Track delivery with agency partners to ensure alignment with plans.
  • Identify opportunities, drive operational excellence, and adopt innovative solutions at scale.
  • Proactively plan activities to ensure timely execution and manage timelines and budgets.
  • Utilize tools to track progress, manage risks, and meet business needs.
  • Prepare project materials and ensure proper documentation and follow-up.

Job description

Content Project Manager – Contract Position – HIRING ASAP

Location: Dublin, Ireland - 2/3 days per week in office

Start Date: ASAP

Duration: 6-month contract with extension

Daily Rate: €320 - €360 per day PAYE

Summary

We're looking for a Publications & Content Manager who can be accountable for high-quality execution and management of therapeutic area aligned publication plans and content programs. Compelling and compliant scientific content, strategized in partnership with Portfolio Scientific Communications has the potential to enable industry-leading launch excellence and change the course of clinical adoption.

This role will embrace a mindset of accountability and strive to exceed expectations amongst enterprise stakeholders for compelling scientific content and publication programs by actively identifying and managing/ mitigating risks to successful outcomes.

Requirements
  • 2+ years of pharmaceutical industry or medical communications agency experience or post-university experience desirable
  • Advanced project management skills
  • Strong financial and business acumen
  • Experience in Medical Affairs/Medical Services leadership delivery roles or providing services to large pharmaceutical organization desirable
  • Experience of working in an international environment.
  • Exemplary interpersonal and listening skills
  • Ability to work with demanding professionals
  • Strong attention to detail
  • Team player
  • Flexible with difficult timelines
  • Advanced understanding of business processes
  • Track record of operational effectiveness or operational innovation.
Responsibilities
  • The remit of responsibilities centers on globally applicable content elements aligned to the Scientific Communications Platform (SCP), which must be delivered in adherence with internal and external guidelines as well as regulatory compliance (e.g., Global Publication Practice). This role plays an active role in managing and coordinating cross-functional and enterprise stakeholders to heighten the certainty of timely and high-quality deliverables.
  • Critical to success will be exceptional project management expertise and an ability to influence outcomes within a highly matrixed environment. This role will be accountable for taking advantage of innovative approaches and digital technologies for efficient and compliant content development. Successful execution will be measured by faultless, on-time delivery and continuous, innovative improvement and rapid adoption of new technologies and practices (e.g., AI-enabled).
  • Accountable for high-quality scientific communication plan management and right-first-time execution of therapeutic area aligned publication plans and content programs throughout the portfolio asset lifecycle
  • Operate as project management point of contact for assigned content programs and publication plans
  • Collaborate with enterprise stakeholders, internal peers, and cross-functional teams to understand needs, manage and deliver publications and content development plans
  • Partner with AD/Director Scientific Communications, Scientific Writers, and agency partners to track the delivery of tactics in line with publication and content development plans
  • Actively identify improvement opportunities, drive operational excellence, track progress, outcomes and best practices for continuous improvement of delivery
  • Adopt proven, innovative solutions at scale to drive efficiency and improvement to end-state deliverables in line with organization and customer needs
  • Proactive/forward planning of activities aligned to deliverables to ensure timely execution; drive project plans, timelines, and budgets to ensure successful project execution
  • Utilizing appropriate tools, track progress, manage risks, and ensure business needs are met
  • Preparation of project and meeting materials, ensuring accurate documentation/tool update (e.g., DataVision, TOV) and follow-up on action items
  • Actively identify and manage/mitigate risks related to project expectations on quality and timelines to achieve successful outcomes
  • Responsible for adherence to associated compliance related activities and approvals
  • Convey credibility and maintain positive, professional image both internally and externally
  • Ensure quality and compliance with all relevant internal SOPs/guidelines and external regulatory requirements. Build quality systems, training and tracking to ensure all regulatory and internal requirements are fully met and adhered to.
  • Partner with AD Publication Excellence to support with compliance and metrics reporting activities at an enterprise level (e.g., Transfers of Value), as needed
  • Provide operational support for publication management tools (e.g., iEnvision), managing user queries, regular GFR updates, and enabling effective publication planning and tracking across countries, as needed
  • Role model exceptional company values and behaviors, embracing high-challenge conversations, to drive change (ethics, change agent, collaboration, humility)
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