Original listing text, shown exactly as published by the company.
What You’ll Be Doing
- Define and execute project plans, including timelines, milestones, and resource requirements aligned with study objectives
- Review study protocols and response assessment criteria; partner with stakeholders to develop study start-up documentation and activities
- Establish project reporting schedules and provide timely updates to leadership, sponsors, and internal teams
- Communicate clearly with project teams, study sites, and sponsor representatives to ensure alignment and transparency
- Identify critical success factors and manage project tracking, analysis, and reporting
- Coordinate cross-functional resources and partner with departmental leaders to ensure appropriate training and delivery excellence
- Manage financial aspects of projects, including forecasting, billing, scope changes, and pass-through costs
- Maintain a thorough understanding of project contracts and support revenue reporting requirements
- Ensure adherence to SOPs; collaborate with Quality Assurance on clarifications, deviations, and documentation
- Lead and develop project teams, setting clear expectations and supporting performance consistency and quality outcomes
- Provide coaching and input on team member performance in partnership with functional managers
- Support Business Development activities, including capability presentations and participation in client and investigator meetings
- Oversee project closeout activities, including submission coordination and final deliverables
- Perform supervisory responsibilities where applicable, including hiring support, performance management, and team development
- Drive continuous improvement by reviewing and contributing to SOP updates and departmental standards
What We Look For
- Bachelor’s degree or equivalent experience in life sciences, pharmacy, nursing, or a related healthcare field
- Proven project management experience within clinical development or investigational medications
- 1–3 years of experience in clinical trials within a CRO or pharmaceutical research organization, ideally in a project management capacity
- Working knowledge of GCP/ICH guidelines and FDA regulations
- Experience in clinical adjudication strongly preferred
- Proficiency with tools such as Microsoft Word, Excel, Access, and Project
- Strong interpersonal, communication, and stakeholder management skills
- Demonstrated organizational, leadership, and problem-solving abilities
- Ability to manage multiple priorities and maintain a high level of professionalism in a fast-paced environment
- Commitment to quality, accuracy, and continuous improvement
At Clario, a part of Thermo Fisher Scientific, we put people first, always. We are united and driven by patients, committed to making a difference, and continuously innovating to shape the future of clinical trials. Join us and be part of a team that transforms lives through science and technology.
