Project Manager

Alliance For MultiSpecialty Research LLC US,

About The Position

The Project Manager is responsible for the overall coordination and management of large scale, complex multi-site clinical projects/ studies from start-up through close out of studies. To consistently embody AMR Clinical’s Core Values: United We Achieve, Celebrate Diverse Perspectives, Do the Right Thing, Adapt and Persevere.

Requirements

  • Bachelor’s degree in applicable field of study (Business, Healthcare Management, etc.)
  • Project management experience is required
  • A minimum of 5+ years of previous experience in clinical research project management and/or clinical operations, possessing the knowledge, skills and abilities to perform this job.
  • Vast knowledge of clinical trials, regulatory requirements, laws, and guidelines.
  • Prior experience working with PI’s and clinical research team.
  • Lead, motivate and coordinate teams to achieve excellent outcomes.
  • Plan and deliver a persuasive presentation.
  • Advance computer software knowledge in various programs, i.e. Word, excel, etc.
  • Excellent task management and prioritization skills.
  • Strong verbal and written skills
  • Strong listening skills
  • Great interpersonal skills
  • Keen and acute attention to detail
  • Ability to work independently and demonstrate initiative.
  • Positive, collaborative, and team-oriented.
  • Ability to work in a fast-paced environment
  • Excellent follow-up skills.
  • Exhibit good judgment.
  • Consume, interpret, and understand complex data.
  • Fluent in English.

Nice To Haves

  • Master’s degree preferred.

Responsibilities

  • Project management activities for complex and/or multi-site trials across the AMR network
  • Plan and lead internal/external meetings with applicable stakeholders.
  • Proactively monitor progress, identify hurdles, and collaboratively develop creative solutions for obstacles to complete projects on time and within budget.
  • Liaison with Sponsor/CRO throughout the study from start-up to completion to ensure seamless study operations.
  • Ensure all clinical study management and project deliverables are completed to the sponsor’s satisfaction, ensuring quality deliverables are on time and per sponsor expectations.
  • Ensure quality and timeliness on all projects.
  • Lead team by demonstrating critical thinking skills, problem-solving, and resolution.
  • Manage external vendors that will be utilized by sites by assessing feasibility, overseeing start-up, and conducting a study.
  • Collaborate with General Manager and Site managers to develop, execute, and track the progress of studies.
  • Ensure all multi-site projects are executed according to the project plan and ELT expectations.
  • Identify and mitigate fundamental issues on the project, make sound business decisions, and ensure solutions are appropriately vetted and implemented.
  • Develop accurate resource requirement projections for each project.
  • Recommend, design, develop, and implement innovative processes to impact clinical trial management.
  • Manage AMR contracted vendors that offer clinical study services.
  • Engage the Business Development team to ensure a clean handoff of awarded studies.
  • In collaboration with BD, participate in feasibility studies and planning for multi-site and complex trials.
  • Communicate regularly with Business Development and Quality Assurance.
  • Identify and address quality-related matters with QA across the projects assigned.
  • Provide timely and accurate KPI reporting to ELT.
  • Use KPI analysis to identify opportunities to improve operating results.
  • Work with site leadership to develop and implement processes to improve clinical trial execution capabilities.
  • Other duties as assigned.
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