Project Manager

CRS

. Plan, coordinate, and oversee all stages of clinical trials, including project planning, budgeting, resource allocation, execution, and closeout .

Posted 11/9/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical project management, ensuring compliance with protocols, SOPs, and regulatory requirements while effectively coordinating all stages of clinical trials. Strong communication and problem-solving abilities support collaboration with stakeholders and the successful execution of multiple projects.

Highest-signal resume keywords

Clinical Project ManagementRegulatory ComplianceProject Management Software ProficiencyStakeholder CommunicationRisk Mitigation Strategies

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trials PlanningProject BudgetingResource AllocationData ManagementProject Execution

Soft Skills

Excellent CommunicationInterpersonal SkillsProblem-Solving SkillsAdaptability

Certifications & Qualifications

Master’s DegreeRelevant Certification

Industry Keywords

Contract Research OrganizationBiotechPharmaceuticalGood Clinical PracticeSOPs

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Plan, coordinate, and oversee all stages of clinical trials, including project planning, budgeting, resource allocation, execution, and closeout
Ensure clinical trials comply with protocols, SOPs, GCP, and applicable regulatory requirements
Serve as the primary contact for sponsors, investigators, and stakeholders
Provide timely and accurate project updates
Identify project risks and develop and implement mitigation strategies
Collaborate with internal teams and external vendors to meet project goals
Oversee data management activities and ensure clinical trial data accuracy and integrity
Conduct regular project meetings and document and follow up on actions and decisions
Prepare and present project reports to senior management and stakeholders
Complete all mandatory training on time and according to company requirements

Requirements

What you’ll need

Bachelor’s degree in a life science or related field
Master’s degree or relevant certification preferred
Minimum of 5 years of experience in clinical project management within a Contract Research Organization (CRO), biotech, or pharmaceutical company
In-depth understanding of clinical trials, including planning, execution, and regulatory requirements
Strong project management skills, with the ability to manage multiple projects simultaneously
Excellent communication and interpersonal skills
Strong problem-solving skills and the ability to adapt to changing circumstances
Proficiency in project management software and other relevant tools
Must be authorized to work in the United States; employer participates in E-Verify

Benefits

Comp & perks

Fully remote position
Occasional domestic travel for company meetings, audits, etc.