Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Worldwide Clinical Trials

Project Manager

Worldwide Clinical Trials

Project Manager coordinating Phase I–IV clinical trials for Worldwide Clinical Trials, a global CRO. Managing technical, financial, operational, and cross-functional project delivery.

Posted 8/20/2026full-timeRemote • Florida • 🇺🇸 United StatesMid-LevelSenior💰 $112,000 - $222,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates extensive experience in managing clinical trials across all phases, with a strong understanding of project management processes and ICH Guidelines. Proven ability to lead teams, coordinate resources, and ensure project deliverables meet quality and regulatory standards.

Highest-signal resume keywords
Clinical Project ManagementICH Guidelines KnowledgeGCP ComplianceTeam LeadershipDrug Development Process

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
Clinical Trial ManagementProject Management ProcessesData InterpretationContingency PlanningResource ManagementProject PlanningRegulatory RequirementsClinical DevelopmentMulti-Office Project ManagementProblem-Solving
Soft Skills
Effective TeamworkConflict ResolutionCommunication SkillsSelf-MotivationOrganizational Skills
Certifications & Qualifications
University/College Degree in Life ScienceCertification in Allied Health Profession
Industry Keywords
Clinical TrialsPharmaceutical IndustryCROHealth Care SettingClient Needs

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Manage one or more allocated Phase I through IV clinical trials that may be local, regional, or global in scope
  • Coordinate and manage clinical trials from start-up through close-out activities
  • Direct the technical, financial, and operational aspects of projects
  • Work with functional area leads to identify and evaluate fundamental project requirements
  • Interpret data on complex issues
  • Conduct contingency planning and implement rescue strategies where needed
  • Ensure solutions are implemented
  • Ensure project deliverables meet customer time, quality, cost, and contract expectations
  • Lead core project team members and facilitate their ability to lead extended or complete project teams
  • Lead cross-unit coordination, both internal and external, including subcontractors
  • Define and manage project resource needs with functional heads
  • Establish contingency plans for key resources
  • Ensure successful design, implementation, tracking, and revision of project plans
  • Promote effective teamwork and resolve conflicts as needed
  • Ensure appropriate communication on project-related matters with Project Management Management

Requirements

What you’ll need
  • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution, or equivalent combination of education and experience
  • Minimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks
  • Alternatively, more than five (5) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries
  • Proven ability and demonstration of relevant experience and skills in clinical development
  • Thorough knowledge of project management processes
  • Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements for clinical development programs
  • Available for domestic and international travel, including overnight stays
  • Valid current passport required
  • Ability to drive and have a valid driver’s license
  • Fluent in local office language and in English, both written and verbal
  • Broad knowledge of drug development process and client needs
  • Demonstrated ability to handle multiple competing priorities and utilize resources effectively
  • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system
  • Demonstrated ability to lead by example and encourage team members to seek solutions
  • Excellent communication, planning, organizational, problem-solving, and self-motivation skills
  • Experience managing projects in a multi-office environment

Benefits

Comp & perks
  • Competitive benefits package depending on location
  • Transparent compensation and pay equity