Note: The job is a remote job and is open to candidates in USA. Signant Health is a global evidence generation company supporting clinical trials through technology, scientific expertise, and operational support. The Project Manager - Advisory plans, executes, and completes clinical trial projects while managing budgets, timelines, resources, risks, client relationships, system delivery, and project status reporting.
Responsibilities
- Manage and lead initial project delivery tasks, including the software development lifecycle (SDLC) of simple to medium complexity studies
- Ensure project systems are built and released in accordance with client expectations; lead the project system change control process
- Support implementation of complex, multi-product projects as needed
- Manage projects in accordance with established timelines, budgets, quality standards, and contractual requirements
- Review, approve, and maintain project and corporate systems and documentation
- Handle client escalations independently; work with internal and client teams to resolve issues and escalate as appropriate in a timely manner
- Serve as the primary contact for customers on assigned projects; ensure quality of communication with clients in terms of cadence, content, and audience
- Manage financial health of assigned projects, including vendor services, licensing, payments, invoicing, devices, resource assignments, and vendor management activities
- Collaborate with other functional areas to ensure project delivery meets timelines and client expectations within budget
- Identify and document Incident Reports with Quality Management; coordinate client notification and closure
- Report project status updates to internal and external stakeholders
- Demonstrated ability to lead through influence
- Capable of weighing risks and making decisions that align with Signant values and strategy
- Manage customer escalations effectively, with follow-up and closure
Skills
- Bachelor's degree or equivalent professional experience
- Proven experience in a Project Management role or equivalent
- Understanding of the software development life cycle and specification and configuration of software products
- Demonstrated ability to manage multiple projects simultaneously with excellent time management, communication (oral and written), and organizational skills
- Detail-oriented with focus on first-time quality delivery
- Proficiency with MS Office Suite (Word, Excel, MS Project, PowerPoint)
- Ability to communicate effectively with all levels of the organization; comfortable presenting to diverse and large audiences
- Proven ability to direct project activities, ensure customer satisfaction, and adhere to study budgets
- Must show initiative and be able to work independently as needed
- Background in pharmaceutical, medical device, medical education, or CRO industries
- Experience with clinical trials, pharmaceutical industry, or life sciences
- Knowledge of the clinical research environment and Good Clinical Practice (GCP) principles
- Project Management Professional (PMP) or equivalent certification
- Willingness to travel for business (overnight trips expected quarterly)
Benefits
- Opportunities to learn, take ownership, and drive meaningful innovation
- Collaborative, global environment
- Purpose-driven work
- Smart colleagues and the opportunity to help shape the future of clinical research and digital health
Company Overview
Company H1B Sponsorship