Project Manager

Veeda Lifesciences

is seeking a Project Manager based in Europe for its growing international hematology/oncology Clinical Trials program.

This is a full-time job.

Job overview: The Project Manager (PM) is accountable for successful execution of clinical studies by effectively managing of project plans, budgets, stakeholder relationships, monitoring project progress, and ensuring compliance with regulatory standards to achieve successful study delivery throughout the project lifecycle

Main responsibilities: − Acts as the internal Sponsor’s representative − Develops and maintains the Responsibility Matrix, outlining the responsibilities amongst key stakeholders involved in a given study − Develops study specific Project Plans including e.g., Project Team Contacts Lists, Project Timelines, Communication Plans, Risk Assessment and Management Plans, Performance Monitoring Plans and Tools, Budget Reconciliation, Vendor Oversight Plan, Issues Escalation Plans − Maintains study specific Project Plans with the input of key stakeholders, throughout the study − Acts as the budget and contract owner − Tracks all items related to budget and client contract completion status − Acts as the Sponsor Calls Lead; coordinates the development of material to be presented, prepares meeting minutes and distributes to the Study Management Team − Is accountable for pre- and post- Study Management Team meetings − Monitors study progress to ensure compliance with and adherence to the Project Plan and to identify, evaluate and rectify problems − Continuously motivates study team members to accomplish project goals on time with a high degree of quality

Job Requirements: -Bachelor’s degree in natural or health sciences, business management or a related field. -Desirable: Postgraduate studies in a relative field or certification in Project Management Professional (PMP) or equivalent -At least 2 years of experience as a Project Manager with proven involvement in Phase II and Phase III clinical trials. Proven track record of managing multiple studies simultaneously -Desirable: Advanced knowledge of ICH GCP and regulatory requirements and / or Site monitoring and clinical quality compliance experience Desirable: Experience in managing or coordinating international multi-center trials / lab data −Excellent command / highly proficient in spoken and written English −Excellent verbal and written communication skills, strong attention to detail −Advanced user of Microsoft Office Suite of tools −Experience in using project management software −Must work well independently and be self-motivated −Strong organizational and planning skills −Willingness to travel up to 20% of time, including domestic and international travel

Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.