Clinical Lead – Clinical Trial Manager

Emerald Clinical

. Oversee clinical trials from start-up to close-out .

Posted 10/6/2026full-timeRemote • United StatesSenior💰 $130,000 - $160,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in overseeing clinical trials, ensuring compliance with GCP and FDA regulations, and managing study timelines and budgets. Proven ability to lead site selection, mentor staff, and maintain data integrity throughout the trial process.

Highest-signal resume keywords

Clinical Trial ManagementGCP ComplianceFDA RegulationsRenal ExperienceCCRA Certification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial OversightSite SelectionFeasibility AssessmentProtocol AdministrationMonitoringStudy Progress ManagementBudget ManagementData IntegrityProject ManagementOncology Experience

Soft Skills

LeadershipProblem-SolvingCommunicationCollaborationMentoring

Certifications & Qualifications

CCRA CertificationCCRP Certification

Industry Keywords

Clinical TrialsGCPFDASOPsRenalOncologySite ManagementStakeholder ManagementStudy TimelinesClinical Trial Best Practices

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Oversee clinical trials from start-up to close-out
Lead site selection and feasibility assessments with CRAs and investigators
Manage study timelines, budgets, and deliverables
Provide oversight of protocol administration, site initiation, monitoring, and study progress
Collaborate with sponsors, investigators, internal stakeholders, and project teams
Ensure compliance with GCP, FDA regulations, and company SOPs
Train and mentor CRAs and site staff
Ensure protocol adherence and data integrity

Requirements

What you’ll need

Renal experience
Bachelor’s degree in a science-related field (RN preferred) with industry experience
1–2 years as a Clinical Trial Manager/Clinical Lead
Strong background in monitoring and site management
Preferably experience in oncology or other complex indications
CCRA or CCRP certification strongly preferred
Excellent knowledge of GCP, FDA regulations, and clinical trial best practices
Ability to manage multiple projects, timelines, and stakeholders efficiently
Strong leadership, problem-solving, and communication skills
Willingness to travel up to 20% as required

Benefits

Comp & perks

Competitive compensation with a tailored salary and benefits package
Hybrid or remote working arrangements, depending on location and role
Learning opportunities and access to a global network of scientific leaders
Employee wellbeing programs and initiatives supporting work-life balance, health, and team connection
Global engagement surveys
Recognition programs
Team-building events
Exposure to diverse international projects and clients