Global Trials Optimization PM I (Remote)

Syneos Health, Inc.; Alaska; Hybrid; USD 81,000 - 145,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401k match

Employee stock purchase plan

Bonus eligibility

Paid time off

Job summary

Syneos Health is recruiting for a Global Trials Optimization Specialist / Project Manager I (Sponsor Dedicated/Remote - US only). The role supports feasibility, recruitment planning, and in-life optimization across global studies, partnering with trial teams, vendors, legal, analytics, and other stakeholders.

You will translate trial goals and enrollment insights into practical strategies, author initial reports, and manage performance analyses to ensure timely study execution.

Qualifications

• Experience supporting clinical trials, feasibility, recruitment planning, enrollment strategy, or trial optimization.
• Strong ability to gather, interpret, and apply data to support planning and decision-making.
• Experience coordinating timelines, deliverables, stakeholder reviews, and cross-functional inputs.
• Ability to work with clinical trial teams, vendors, legal, analytics, and other business partners.
• Strong written communication skills, including the ability to develop clear reports, plans, updates, and study-facing materials.
• Detail-oriented approach with the ability to manage multiple priorities in a fast-paced clinical research environment.

Responsibilities

• Gather data, benchmarks, and modeling inputs to support feasibility and trial optimization planning.
• Support program review development, including content review and escalation of requirements as needed.
• Plan timelines for validation, deliverable development, stakeholder alignment, presentation preparation, and country validation requests.
• Support validation and Clinical Trials Allocation Committee activities, including scenario planning, risk table inputs, validation review, modeling updates, and final allocation requests.
• Author the initial Global Trials Optimization Report and maintain subsequent report updates throughout the trial lifecycle.
• Complete recruitment needs assessments and ensure trial-level GTO reports remain current and actionable.
• Lead early recruitment and retention planning during feasibility, including inputs for project cost estimates.
• Develop initial recruitment needs assessments and, where applicable, program-level recruitment budget estimates.
• Submit vendor requests and prepare recruitment and retention plans.
• Partner with legal on concept reviews, vendor proposal reviews, scope of work finalization, and material or tactic reviews.
• Ensure recruitment and retention plans, including enrollment support materials, are implemented effectively.
• Oversee enrollment support material development and tactic execution.
• Provide required materials to the Metrics, Analytics & Performance team to support accurate Study Optimizer plan entry.
• Request and manage appropriate system updates as trial needs evolve.
• Partner with study teams to identify enrollment challenges, assess risks, and recommend potential mitigations.
• Manage routine enrollment support materials and vendor activities.
• Monitor enrollment performance and prepare standard reporting.
• Analyze performance trends and identify opportunities for enhanced support.
• Coordinate enhanced enrollment support activities, which may include rescue site and country activities, external recruitment and retention booster meetings, and related materials.

Skills

Clinical trials

Feasibility

Enrollment planning

Cross-functional

Data interpretation

Timeline coordination

Stakeholder reviews

Reporting

Attention to detail

Job description

Syneos Health is recruiting for a Global Trials Optimization Specialist / Project Manager I (Sponsor Dedicated/Remote - US only). The role supports feasibility, recruitment planning, and in-life optimization across global studies, partnering with trial teams, vendors, legal, analytics, and other stakeholders.

You will translate trial goals and enrollment insights into practical strategies, author initial reports, and manage performance analyses to ensure timely study execution.