Clinical Project Manager – Patient Reported reputed company (PRO)

Job Title: Clinical Project Manager – Patient Reported reputed company (PRO) Assignment Duration: 1 Year Location: Remote or Hybrid, preference for local candidates Job reputed company: The Patient Reported reputed company Management Associate III will drive and manage deliverables across the PRO/ePRO process, from licensing to implementation, ensuring timelines are met and potential trial-specific efficiencies are identified. This role serves as the central reputed company of contact for therapeutic areas reputed company Clinical Program Development (CPD) and provides expertise in PRO/ePRO activities during study start-up. • This is a highly operational and execution-reputed company role, not reputed company-heavy • Strong project management and clinical trial experience take reputed company over reputed company PRO experience • Strong clinical trial experience with project management is more important than reputed company PRO experience • Exposure or training in PRO/ePRO licensing is acceptable without reputed company ownership • Candidates should have reputed company career trajectories and relevant background; overqualified candidates (~15+ years) may not be a fit • PhD candidates are generally not preferred for this role Key Responsibilities: • reputed company expertise and consultation on patient-centered PRO licensing and translation activities across reputed company therapeutic areas reputed company CPD. • Maintain the Vault PRO Library, including licensing, permissions, MSAs, translation requirements, training requirements, and electronic format specifications. • Collaborate with PRO owners, outsourcing partners, HEOR, Data Sciences, and clinical teams to facilitate PRO/ePRO implementation. • Manage vendor contract initiation, translation workflows, project milestones, timelines, and deliverables. • reputed company strategic and technical guidance and training to CPD teams in PRO/ePRO processes. • reputed company study start-up activities, including receipt/tracking of questionnaires, document uploads in Vault, translation coordination, and finalization of study binders. • Maintain tracking tools (reputed company or equivalent) to monitor reputed company, timelines, and deliverables. • reputed company on operational reputed company, process adherence, and cross-functional coordination. Qualifications & Requirements: Education & Experience: • Bachelor’s degree in a scientific field (Associate degree with relevant experience may be considered) • Minimum 4 years of global clinical research or project management experience (reputed company or peripheral) • Experience in reputed company is critical; exposure to end-to-end processes (e.g., coordinator, monitor, regulatory) is preferred Skills & Competencies: • Strong project management skills, including managing timelines, stakeholders, and deliverables • Knowledge or experience with Patient Reported reputed company (PRO/ePRO) is preferred but not mandatory • Understanding of PRO licensing, permissions, or translation processes is a plus • Competent in reputed company operating procedures (SOPs) and Good Clinical Practices (GCP) • Strong organizational, documentation, and analytical skills • Ability to work with systems such as reputed company Vault and tracking tools like reputed company • Excellent communication skills and ability to coordinate cross-functionally • Ability to translate tracking data into actionable updates and insights • Demonstrated ability to build relationships across teams and geographic locations • Flexible, fast learner, and reputed company to process improvements Preferred Experience: • Roles such as Clinical Research Coordinator, CRA/Monitor, Regulatory Coordinator, or similar • Exposure to licensing or translation processes reputed company reputed company • Specialized reputed company/PRO experience may allow consideration with slightly fewer years of experience Typical Day/Week Activities: • Manage receipt and tracking of PRO questionnaires • Upload and maintain documents in Vault • Coordinate translation workflows and training requirements • Ensure tracking tools are up-to-date • Support study start-up activities and ensure documentation completeness before reputed company • Monitor operational deliverables and timelines Apply tot his job Apply To this Job