Role Description Hey there! We’re looking for a Digital Project Manager for a leading client in the healthcare sector. If you are highly organized, solutions-driven, and great at leading cross-functional teams, keep reading! - Lead digital projects end-to-end, from kickoff through delivery - Build project plans defining scope, timelines, milestones, and resources - Coordinate online campaign execution with creative and content teams - Manage stakeholders, vendors, and internal teams to ensure alignment - Track budgets, resources, and project performance - Monitor timelines and proactively resolve blockers or delays - Ensure deliverables meet quality standards through regular reviews - Maintain project documentation (plans, reports, change requests) - Provide clear status updates and communicate progress to stakeholders - Identify opportunities for continuous improvement and implement best practices Qualifications - Bachelor’s degree in a relevant field (Project Management, Business, IT, or similar) - Proven experience managing digital projects - Strong leadership, organization, and prioritization skills - Excellent communication and stakeholder management abilities - Ability to manage budgets, timelines, and multiple moving parts - Strong problem-solving and decision-making skills - Proficiency with project management tools (Asana, Jira, Trello, Monday, etc.) Requirements - Project management certification (PMP or similar) - Familiarity with digital technologies, platforms, and marketing trends - Experience working with third-party vendors and cross-functional teams - Strong reporting and presentation skills Benefits - 2 weeks of PTO - Salary in USD - Career growth opportunities - Opportunity to work in a collaborative environment

• Leading the preparation, submission, and maintenance of regulatory documents for EU CTIS submissions. • Providing expertise and guidance on regulatory requirements and standards to internal teams. • Interfacing with regulatory agencies to address inquiries, submissions, and approvals. • Monitoring changes in regulations and guidelines to ensure compliance and mitigate risks. • Collaborating cross-functionally to support regulatory aspects of clinical trial planning and execution.

• Assist the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities) • May support a single study or multiple studies • May lead a study with limited scope (e.g., Survival Follow-up) • May be responsible for tracking study timelines and will be proficient in project management tools • May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives.

• Own the overall strategy, roadmap, and success metrics for Thyme Care’s provider intervention and drug incentive programs • Partner closely with Commercial Directors to identify target practices • Serve as a key client-facing leader for provider intervention programs