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Syneos Health

Project Specialist, Finance, Clinical Research

Syneos Health

. Plan, direct, create, and communicate clinical study timelines, ensuring milestones are met and projects stay on track .

Posted 10/8/2026full-timeRemote • ArgentinaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical project management, including planning, executing, and monitoring clinical trials while ensuring compliance with SOP, GCP, and regulatory standards. Proficient in budget management, team collaboration, and developing recruitment strategies to meet project goals.

Highest-signal resume keywords
Clinical Project ManagementGood Clinical Practice (GCP) CertificationSOP ComplianceBudget ManagementTeam Collaboration

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ProcessesProject PlanningTimeline ManagementPerformance MonitoringRecruitment Strategy DevelopmentData ManagementRegulatory ComplianceContract NegotiationExpenditure MonitoringProblem-Solving
Soft Skills
Organizational SkillsTime ManagementCommunication SkillsInterpersonal SkillsAttention to Detail
Tools & Technologies
Microsoft Office SuiteExcelWordPowerPoint
Certifications & Qualifications
Clinical Project Management CertificationGood Clinical Practice (GCP) Certification
Industry Keywords
Clinical TrialsRegulatory StandardsClinical Study ProceduresOperational AspectsTrial Site Selection

About the role

Key responsibilities & impact
  • Plan, direct, create, and communicate clinical study timelines, ensuring milestones are met and projects stay on track
  • Gather input from clinical, regulatory, and data management teams to create comprehensive plans for timely deliverables
  • Standardize clinical study procedures and implement best practices across trials
  • Oversee and resolve operational aspects of clinical trials in compliance with SOP, GCP, and country regulations
  • Select clinical trial sites and vendors, negotiate contracts, and manage relationships
  • Prepare clinical trial budgets, monitor expenditures, and keep studies within budget
  • Monitor trial progress, track key performance indicators, and address deviations from plan
  • Implement and prepare clinical development strategies aligned with project goals
  • Develop trial recruitment strategies and monitor enrollment progress

Requirements

What you’ll need
  • High school diploma or equivalent required
  • Associate's degree or higher in a related field preferred
  • Minimum of 3 years of experience in clinical project management or a related field
  • Strong understanding of clinical trial processes and regulations
  • Experience with SOP, GCP, and country-specific regulations
  • Certification in Clinical Project Management or related field preferred
  • Good Clinical Practice (GCP) certification preferred
  • Excellent organizational and time management skills
  • Strong communication and interpersonal skills
  • Ability to work effectively in a team environment
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Attention to detail and problem-solving skills
  • Ability to adapt to changing priorities and work under pressure
  • Equivalent experience, skills, and/or education will also be considered

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition
  • Total rewards program
  • Inclusive culture
  • Reasonable accommodations, when appropriate