Clinical Study Manager

Worldwide Clinical Trials

. Manage one or more allocated Phase I through IV clinical trials, which may be local, regional, or global in scope .

Posted 9/23/2026full-timeSan Antonio • Texas • United StatesMid-LevelSenior💰 $60,000 - $119,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing Phase I through IV clinical trials, ensuring project deliverables meet customer expectations while promoting effective teamwork and communication. Possesses strong problem-solving abilities and experience in multi-office project management within the clinical pharmaceutical industry.

Highest-signal resume keywords

Clinical Project ManagementMulti-Office Project ManagementContingency PlanningTeam LeadershipExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementProject PlanningData InterpretationResource ManagementProject Tracking

Soft Skills

Problem-SolvingTeam MotivationConflict ResolutionOrganizational SkillsSelf-Motivation

Certifications & Qualifications

University/College DegreeNursing CertificationMedical Technology CertificationLaboratory Technology Certification

Industry Keywords

Clinical TrialsPharmaceutical IndustryProject DeliverablesCross-Unit CoordinationMatrix System

About the role

Key responsibilities & impact

Manage one or more allocated Phase I through IV clinical trials, which may be local, regional, or global in scope
Coordinate and manage clinical trials from start-up through closeout
Direct the technical, financial, and operational aspects of projects
Work with functional area leads to identify and evaluate project requirements
Interpret data on complex issues
Conduct contingency planning and implement rescue strategies when needed
Ensure solutions are implemented
Ensure project deliverables meet customer time, quality, cost, and contract expectations
Lead core project team members and facilitate leadership of extended or complete project teams
Lead internal and external cross-unit coordination, including subcontractors
Define and manage project resource needs and establish contingency plans for key resources
Ensure successful design, implementation, tracking, and revision of project plans
Promote effective teamwork and resolve conflicts
Ensure appropriate communication on project-related matters with CSM Management
Work under the direct supervision and guidance of the Site Director; does not supervise other staff

Requirements

What you’ll need

Experience in managing projects in a multi-office environment
Ability to handle multiple competing priorities and utilize resources effectively
Ability to inspire effective teamwork and motivate staff within a matrix system
Ability to lead by example and encourage team members to seek solutions
Excellent communication, planning and organizational skills
Self-motivated with excellent problem-solving skills
Required: University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology), or equivalent combination of education and experience
Preferred: Minimum of five (5) years of clinical pharmaceutical industry experience, including clinical project management tasks

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Transparent compensation and pay equity