Project Manager - Clinical Trial Transparency Job in Xogene Services Llc

Position Overview Offering a suite of transparency services, Xogene is a leader in innovative technologies and expert services to meet global clinical trial transparency. Our team of experts provide comprehensive services to the pharmaceutical, biotechnology, and medical industries. Our consulting and strategic services help our clients navigate complex challenges and make informed decisions. As we continue to expand, we are seeking an experienced Project Manager to join our dynamic team and contribute to our ongoing growth and success. The Project Manager will be responsible for overseeing and delivering complex projects for our clients across various offerings. You will drive project success by effectively managing timelines, budgets, resources, and stakeholders. The ideal candidate has a proven track record of successfully managing complex projects and possesses excellent leadership, communication, and problem-solving skills. Key Responsibilities Develop and execute comprehensive project plans, including defining project scope, objectives, deliverables, timelines, and resource allocation. Coordinate and monitor project activities to ensure adherence to quality standards, deadlines, and budgetary constraints. Build strong relationships with clients, internal teams, and external stakeholders. Collaborate closely with clients to understand their requirements, address concerns, and provide regular project updates. Effectively manage and communicate project expectations to all stakeholders. Prepare meeting agendas, take meticulous notes and follow-up reports, manage action items and communicate all with stakeholders and management as needed. Identify and manage project risks, issues, and changes. Implement mitigation strategies and contingency plans as needed. Lead and motivate cross-functional project teams, providing clear direction, guidance, and support. Contribute to the development and enhancement of project management methodologies, tools, and best practices. Seek opportunities for process improvement and efficiency gains to drive better project outcomes. REQUIREMENTS Qualifications and Experience Bachelor's degree in a relevant field (S.T.E.M. preferred); advanced degree or certification in project management is a plus. 5 years in project management with exposure to clinical research. 1-2 of years of clinical research and/or regulatory affairs management. Demonstrated ability to prioritize and manage multiple projects concurrently while meeting deadlines and budgets. Excellent leadership and team management skills, with the ability to motivate and inspire team members. Strong analytical and problem-solving skills, with a keen attention to detail. Proficiency in project management software and tools. PMP certification or related training desired but not mandatory. Strong knowledge of clinical trials preferred.