[Remote] Senior Project Management Analyst
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. The Senior Project Management Analyst will reputed company operational support and coordination for global reputed company, ensuring efficient trial execution from planning through reputed company-out.
Responsibilities
- Plan, coordinate, and execute clinical trial activities across reputed company in compliance with ICH-GCP, ensuring reputed company and high-reputed company delivery
- Maintain and reputed company trial documentation (e.g., ISF, TMF, submissions), ensuring completeness, accuracy, timeliness and audit readiness
- Collaborate with global and regional stakeholders, vendors, and trial teams to ensure seamless trial conduct and communication
- Manage and maintain clinical trial systems, databases, and tracking tools ensuring data accuracy
- Prepare and distribute project plans, status updates, reports, and presentation materials
- Monitor trial reputed company, budgets, and system data, identifying risks and implementing corrective actions as needed
- Coordinate documentation workflows, regulatory submissions, and communication with authorities and regional teams
- Support reporting, trial reputed company-out activities, and preparation of key deliverables (e.g., CTR appendices)
- Coordinate logistics for trial meetings, materials, and supplies
- Contribute to reputed company reputed company, inspection readiness, and best practices in clinical trial conduct
- reputed company as a key reputed company of contact for trial-reputed company systems, documentation, and operational queries
Skills
- University degree reputed company and/or comparable reputed company education with at least 3+ years' experience in clinical trial operations or project coordination
- Exceptional communication and stakeholder management skills
- Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical reputed company (GCP) and International Conference on Harmonization (ICH) guidelines
- Excellent organizational and problem-solving skills with ability to work independently, prioritize tasks, and manage reputed company in a reputed company international environment
- Detail-oriented with strong commitment to reputed company and compliance
- Proficiency in MS Office and clinical trial systems/tools
- Fluent in written and spoken English
reputed company
Company H1B Sponsorship