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Syneos Health

Syneos Health

via Remote Rocketship

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Senior Global Project Manager – Sponsor Dedicated

Anywhere
full-time
Posted 11/17/2025
Verified Source
Key Skills:
Global clinical trial planning
Phase II & III trial leadership
Therapeutic area expertise (Immunology, Metabolic, Oncology)
Clinical quality and regulatory compliance
Vendor management
Stakeholder communication and leadership

Compensation

Salary Range

$120K - 180K a year

Responsibilities

Lead and oversee global clinical trial planning, execution, vendor management, patient recruitment, and regulatory compliance to ensure successful trial delivery.

Requirements

Bachelor's degree, proven experience leading Phase II & III global clinical trials in specified therapeutic areas, strong leadership and communication skills, and ability to manage complex clinical trial operations.

Full Description

Job Description: • Lead planning and operational feasibility assessments to ensure realistic and achievable trial timelines • Oversee trial set-up and ensure team alignment across functions including Statistics, Data Management, Medical Writing, and Site Monitoring • Support country allocation and feasibility processes; provide input to optimize site selection and trial readiness • Develop and implement trial-level engagement, recruitment, and risk mitigation plans, integrating patient and site feedback to enhance trial design and participant experience • Coordinate outsourcing of vendor services, supporting vendor identification, selection, and scope-of-work development • Partner with cross-functional teams to ensure readiness across all trial processes — clinical quality, safety monitoring, investigational product management, budgeting, and site support • Facilitate and support responses to regulatory authorities, ethics committees, and other external stakeholders • Ensure all trial team members receive appropriate study-specific and standardized training • Maintain oversight of global clinical trial conduct to ensure compliance with Good Clinical Practice (GCP), internal SOPs, and all applicable regulatory requirements • Oversee patient recruitment progress, risk mitigation, and budget tracking to ensure efficient delivery • Manage amendments to study documentation and related retraining as needed • Ensure effective oversight of vendors and central labs, in collaboration with functional partners • Support ongoing communication and coordination across the clinical delivery network and stakeholders Requirements: • Bachelor’s degree (4-year undergraduate degree) in a relevant field • Proven experience leading Phase II & III global clinical trials • Therapeutic area experience in Immunology, Metabolic, or Oncology (additional TA experience is a plus) • Strong scientific and operational expertise across global clinical trial planning and execution • Exceptional leadership, communication, and stakeholder management skills in complex matrix structures • Ability to strategically plan and drive clinical trial delivery while ensuring patient-focused outcomes Benefits: • Health benefits to include Medical, Dental and Vision • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) and sick time

This job posting was last updated on 11/24/2025

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