Consulting Project Manager - (Danish Speaking)

Location: UK/EU Job Type:

Full-Time Job Description:

We are seeking a Consulting Technology Project Manager to manage client implementation projects for our Pharmacovigilance SaaS solutions. The ideal candidate will be a dynamic client facing services professional with extensive project management experience in the life science technology domain. This is a strategic role requiring deep project management expertise, pharmaceutical domain knowledge, and excellent leadership skills. Key Responsibilities:

* Lead end-to-end project management of client software implementations, upgrades, and integrations.

* Develop and manage project plans, including timelines, budgets, and resource demand, and author project initiation documents.

* Coordinate cross-functional, global teams to ensure successful project delivery. * Serve as the primary point of contact for senior client stakeholders, ensuring clear

communication and strong relationship management. * Ensure the accuracy, reliability, and performance of all project deliverables. * Monitor project progress and performance, identifying and mitigating risks and issues as

they arise. * Facilitate regular project status meetings and provide updates to stakeholders. * Actively manage project scope and costs, ensuring any changes are documented and

approved through formal change control processes. * Develop and maintain comprehensive project documentation, including project

initiation documents, risk management plans, and post-project reviews. * Ensure all projects comply with industry regulations, particularly those related to

pharmacovigilance and data privacy (e.g. GxP, GDPR). * Coordinate and manage interactions with third-party vendors, consultants, and partners

to ensure successful delivery and integration of external components or services. * Support continuous improvement of project management processes, tools, and best

practices within the organization. * Mentor and guide junior project managers and team members, fostering a collaborative

and high-performance team environment. Characteristics:

* Well-organized self-starter with attention to detail. * Excellent client facing communication and problem-solving skills. * Strong written, communication, and interpersonal skills. * A desire to learn about our proprietary products

Essential Experience and Qualifications: * Bachelor''s or master''s degree in computer science, Information Technology, Project

Management, or a related field. * Should be proficient in Danish language skills * 8+ years of experience in project management, with at least 5 years in a senior or lead

role delivering software solutions to pharmaceutical or life sciences clients. * Proven experience managing pharmacovigilance, clinical, or regulatory technology

projects. * Knowledge of pharmacovigilance workflows and regulatory standards (e.g., ICH E2E,

GVP Modules, FDA, EMA). * Expertise in project management methodologies (e.g., Agile, Scrum, Waterfall). * Proficiency in project management tools (e.g., Microsoft Project, Jira, SmartSheet).

Preferred Experience and Qualifications:

* Familiarity with signal detection, case management, and safety databases (e.g., Argus, ARISg).

* Familiarity with cloud-based solutions and big data technologies. * Technical background with experience in software development or IT infrastructure. * Knowledge of regulatory requirements and industry standards for technology solutions. * Certification in project management (e.g., PMP, PRINCE2).

What We Offer:

* Competitive salary * Opportunity to work with a dynamic and innovative team and world-class clients. * Professional development and growth opportunities. * A collaborative and inclusive work environment. * Work from home with limited travel.