Global Trials Optimization Specialist — Remote Project Manager I

Syneos Health; Massachusetts; On-site; USD 90,000 - 130,000; Full time

Job summary

Syneos Health is seeking a Global Trials Optimization Specialist to support feasibility, enrollment strategy, and in-life trial optimization across multiple therapeutic areas. The role emphasizes data-driven decisions to improve study performance on a global scale.

The position requires strong analytical skills, experience in feasibility and recruitment planning, and the ability to coordinate with clinical trial teams, vendors, and legal partners while working sponsor-dedicated and remote in the

Qualifications

• Experience supporting clinical trials, feasibility assessments, recruitment planning, and trial optimization.
• Strong analytical skills with ability to interpret data for decision-making.
• Experience managing timelines, deliverables, and cross-functional reviews.
• Ability to collaborate with study teams, vendors, and analytics partners.
• Excellent written and verbal communication for reports and strategic plans.
• Strong organizational skills in a fast-paced clinical-research environment.

Responsibilities

• Program Feasibility and Trial Optimization: gather data, benchmarks, and modeling inputs for feasibility and optimization planning.
• Recruitment and Retention Planning: lead early planning, draft budgets, and coordinate recruitment materials with stakeholders.
• In-Life Trial Management: monitor enrollment performance, identify risks, and support site/vendor activities.

Skills

Clinical trials

Data analysis

Project management

Cross-functional collaboration

Communication skills

Strategic planning

Job description

Syneos Health is seeking a Global Trials Optimization Specialist to support feasibility, enrollment strategy, and in-life trial optimization across multiple therapeutic areas. The role emphasizes data-driven decisions to improve study performance on a global scale.

The position requires strong analytical skills, experience in feasibility and recruitment planning, and the ability to coordinate with clinical trial teams, vendors, and legal partners while working sponsor-dedicated and remote in the