Senior Clinical Project Manager

INSIGHTEC

Clinical Project Manager leading clinical trial study teams and managing global clinical trial activities. Collaborating with multiple stakeholders to ensure compliance and high-quality data collection.

Posted 7/21/2026full-timeRemote • Florida, Texas • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing global clinical trial activities, including project management, regulatory compliance, and stakeholder engagement. Proficient in clinical study protocol development, data management, and biostatistics interpretation.

Highest-signal resume keywords

Clinical Project ManagementClinical Study Protocol AuthoringMedical Device Clinical ResearchRegulatory Authority InteractionStakeholder Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementBiostatisticsData ManagementClinical Data InterpretationMedical Writing

Soft Skills

LeadershipCommunicationPresentationOrganizational Skills

Industry Keywords

Life SciencesClinical Trial LifecycleInvestigational Review BoardsExternal Clinical VendorsPivotal Trials

About the role

Key responsibilities & impact

Responsible for independently leading the clinical trial study team
Managing global clinical trial activities on pivotal trial
Effectively communicates and guides clinical team members
Partners effectively with R&D, Regulatory, Quality, Marketing/Product stake-holders
Management of all clinical studies including developing project management plans
Identification, qualification, and training of investigators and teams
Responsible for the activities related to IRBs/ECs, and clinical study vendors
Proactively manage the data management and data lock processes
Great site relationships with the PI and coordinator

Requirements

What you’ll need

Bachelor’s degree in a Life Sciences discipline required
Exceptional proficiency in professional English, with advanced medical and scientific writing skills
Demonstrated experience authoring clinical study protocols
Strong presentation and communication skills
Comprehensive knowledge of the medical device clinical trial lifecycle
In-depth understanding of medical device clinical research
Solid understanding of biostatistics and clinical data interpretation
Minimum of 5–6 years of progressive experience in clinical project management
Experience working directly with regulatory authorities
Proven ability to manage and oversee external clinical vendors
Excellent organizational, leadership, and stakeholder-management skills

Benefits

Comp & perks

competitive perks and benefits