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Clario

Clinical Project Manager

Clario

. Lead study startup activities by reviewing protocol requirements, defining project plans, and coordinating documentation with stakeholders .

Posted 10/30/2026full-timeRemote • Costa RicaJuniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in project management within clinical trials, including project planning, financial tracking, and regulatory compliance. Proven leadership abilities in team management, communication, and cross-functional collaboration.

Highest-signal resume keywords
Project ManagementClinical Trials ExperienceRegulatory ComplianceFinancial TrackingLeadership

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
Project PlanningFinancial OversightRegulatory ComplianceClinical TrialsDocumentation Coordination
Soft Skills
LeadershipCommunicationCross-Functional CollaborationCoachingMentoring
Tools & Technologies
Microsoft WordMicrosoft ExcelMicrosoft AccessMicrosoft Project
Industry Keywords
CROGCPICHFDALife Sciences

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Lead study startup activities by reviewing protocol requirements, defining project plans, and coordinating documentation with stakeholders
  • Manage project execution through resource planning, financial oversight, and adherence to SOPs and regulatory guidelines
  • Provide team leadership by setting performance expectations, delivering training, and supporting coaching and mentoring efforts
  • Support business development by contributing to capability presentations and representing Clario at professional meetings
  • Oversee project closeout by coordinating submission activities and ensuring completion of all final deliverables

Requirements

What you’ll need
  • Bachelor’s degree in life sciences, pharmacy, nursing, or related healthcare field, or equivalent experience
  • 1–3 years of clinical trials experience within a CRO or pharmaceutical research organization, preferably in project management
  • Proven expertise in project planning, financial tracking, and regulatory compliance (GCP, ICH, FDA)
  • Strong proficiency in Microsoft Word, Excel, Access, and Project
  • Demonstrated ability in leadership, communication, and cross-functional collaboration

Benefits

Comp & perks
  • Competitive compensation
  • Medical, dental, and vision coverage
  • Flexible and paid time off
  • Remote and hybrid work options
  • Tuition reimbursement
  • Employee assistance and wellness programs