Remote Project Manager II: Trials Leader

Premier Research Group; Northern (KY); À distance; USD 95 000 - 125 000; Plein temps

Résumé du poste

Premier Research is seeking a Project Manager II to join our Specialty team, remotely or onsite in the United States. You will lead and coordinate clinical trial activities across Regulatory, Clinical Operations, Biometrics, and Medical Affairs to deliver milestones on time and within budget.

You will manage timelines, budgets, and resources, report progress to stakeholders, and ensure adherence to Premier Research processes and training requirements.

Qualifications

• Bachelor’s degree preferably in a clinical, biological or science-related field from an accredited college or university, or equivalent combination of education and experience
• 3+ years of relevant experience preferred
• Experience leading teams
• Experience reporting to and managing internal and external stakeholders
• Experience managing timelines
• Experience managing budgets

Responsabilités

• Ensures successful management and coordination of efforts assigned to all members of the project team, including Regulatory, Clinical Operations, Biometrics, and Medical Affairs/Safety, to support milestone achievement and overall project delivery
• Ensures adherence to project budget and scope of work to realize project profitability
• Ensures all project tasks are completed in accordance with project plans and in compliance with standard Premier Research processes, policies and procedures
• Ensures effective communication is maintained and project status reports and monthly progress reports are provided both internally and externally
• Ensures compliance for project-related training
• Ensures adequate resourcing is available to meet project deliverables and milestones

Formation

Bachelor’s degree in science-related field

Description du poste

Premier Research is seeking a Project Manager II to join our Specialty team, remotely or onsite in the United States. You will lead and coordinate clinical trial activities across Regulatory, Clinical Operations, Biometrics, and Medical Affairs to deliver milestones on time and within budget.

You will manage timelines, budgets, and resources, report progress to stakeholders, and ensure adherence to Premier Research processes and training requirements.