Clinical Team Manager

ERGOMED

Clinical Team Manager responsible for operational project management in a mid-sized CRO focused on Oncology and Rare Diseases. Leading teams and ensuring compliance across projects in a fast-paced environment.

Posted 7/2/2026full-timeRemote • North Carolina • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical project management, including risk mitigation, team training, and document development for clinical trials. Proven ability to manage complex studies across multiple regions while ensuring compliance with GCP and SOP standards.

Highest-signal resume keywords

Clinical Research Lead ExperiencePhase 2/3 Trials ManagementRisk Identification and MitigationTeam Training and DevelopmentProject Document Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Project ManagementGCP ComplianceSOP DevelopmentClinical Monitoring Plan DevelopmentCRF Completion GuidelinesStudy Specific Operating ManualCorrective and Preventative MeasuresCo-MonitoringTraining VerificationOperational Project Management

Soft Skills

Effective CommunicationProblem SolvingAdaptabilityLeadershipCollaboration

Industry Keywords

Oncology StudiesRare Disease StudiesCRO EnvironmentClinical TrialsStudy Specific Procedures

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

The Clinical Team Manager will be responsible for operational project management
The CTM proactively identifies, resolves/mitigates, and escalates risks and/or issues to the PM/PD and Head of Clinical Operations as necessary
Verifying and ensuring that project team members (CRAs, Site Managers, CTAs) are trained (e.g., GCP, SOP, indication, protocol, study specific procedures / requirements, etc.) to perform their assignments
Developing, reviewing and revision of project documents (e.g., clinical monitoring plan, CRF completion guidelines, study specific operating manual, study specific forms etc.)
Initiating corrective / preventative measures – e.g., update of study guidance documents, performing re-training, performing co-monitoring, etc.

Requirements

What you’ll need

Extensive clinical research lead experience in multiple studies
Experience in managing Clinical part of studies in more than one region or equivalent study complexities
Experience of phase 2/3 trials, ideally complex studies such as oncology or rare disease
Able to work in a fast-paced small CRO environment and manage multiple projects
A minimum of a science-based bachelor’s degree
Able to work effectively with minimal supervision

Benefits

Comp & perks

Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly, supportive working environment
Opportunity to work with colleagues based all over the world, with English as the company language