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4D Molecular Therapeutics

Clinical Trial Manager

4D Molecular Therapeutics

Clinical Trial Manager facilitating phase 1-3 clinical trials at 4D Molecular Therapeutics, a biotechnology company. Managing operational aspects of trials and ensuring adherence to regulations.

Posted 7/1/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $150,000 - $170,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in clinical trial management, ensuring compliance with ICH GCP guidelines and regulatory requirements. Proficient in managing study milestones, metrics tracking, and training of clinical research staff.

Highest-signal resume keywords
Clinical Trial ManagementICH GCP ComplianceRegulatory Requirements KnowledgeMicrosoft Office Suite ProficiencyMS Project Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Research ExperienceProtocol Execution ManagementStudy Milestone TrackingClinical Study Management SkillsTraining of CRO Staff
Soft Skills
Excellent Communication SkillsCreative Problem-SolvingSound Judgment
Industry Keywords
Biotech IndustryPhase 1-3 Clinical TrialsClinical Trial Activities

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Support the Company's clinical trial activities
  • Manage the day to day operations of one or more phase 1-3 clinical trials
  • Serve as the primary unmasked contact for managing protocol execution
  • Support establishment of study milestones and ensure accurate tracking of study metrics
  • Ensure clinical trials are managed in accordance with ICH GCP, regulations, and protocols
  • Conduct training of CRO study staff, monitors, investigational sites, and service providers

Requirements

What you’ll need
  • B.A./B.S. degree
  • 6+ years of clinical research experience within the Biotech or similar industry
  • At least 2 years directly supporting clinical trial management
  • Knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial management
  • Strong clinical study management skills
  • Excellent communication skills
  • Proven ability in creative problem-solving and exercising sound judgment
  • Proficient computer skills, specifically with Microsoft Office Suite
  • Working knowledge of MS Project

Benefits

Comp & perks
  • Health insurance
  • 401(k) plan
  • Paid time off
  • Professional development opportunities