Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Innovaderm Research Inc.

Project Director, Dermatology and Rheumatology

Innovaderm Research Inc.

. Oversee a portfolio or program of clinical studies and Project Managers assigned to operationalize awarded studies .

Posted 10/9/2026full-timeRemote • North Carolina • United StatesLeadWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates extensive experience in clinical project management, overseeing multinational phase III clinical trials, and ensuring compliance with GCPs, ICH guidelines, and regulatory standards. Proven ability to lead project teams, manage budgets, and drive operational efficiencies while maintaining client satisfaction.

Highest-signal resume keywords
Clinical Project ManagementRegulatory ComplianceBudget ManagementMentoring and CoachingTherapeutic Area Expertise

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Study OversightProject Budget TrackingVendor ManagementRisk Mitigation StrategiesProposal Development
Soft Skills
Effective CommunicationLeadershipPerformance Improvement
Tools & Technologies
Tracking and Analysis Tools
Certifications & Qualifications
PMP CertificationPRINCE2 Certification
Industry Keywords
Good Clinical PracticesHealth Canada RegulationsFDA RegulationsDermatology ExperienceRheumatology Experience

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Oversee a portfolio or program of clinical studies and Project Managers assigned to operationalize awarded studies
  • Ensure studies meet therapeutic or client-specific requirements
  • Represent the company to customers and maintain satisfaction levels
  • Communicate program deliverables effectively
  • Ensure studies progress according to quality standards, SOPs, GCPs, ICH guidelines, and applicable regulations
  • Oversee executed contracts and financial aspects, including study budgets and expenses
  • Maintain and evaluate project progress using timelines and tracking/analysis tools
  • Maintain in-depth therapeutic and/or client-specific knowledge for the assigned portfolio
  • Apply study-specific learning across assigned studies and clients
  • Lead contingency planning and risk mitigation strategies
  • Provide operational input to proposal development and pricing, including operations strategy
  • Drive performance improvement, operational efficiencies, and innovative strategies
  • Provide line management oversight and contribute to Project Management leadership as an operational and therapeutic area expert

Requirements

What you’ll need
  • Bachelor of Science in a relevant discipline
  • At least 15 years industry experience
  • Minimum of 5 years at a CRO
  • At least 10 years of clinical project management experience, including management of all project phases from start up to closure, management of all functional services, and vendor management
  • Experience with mid-size and large studies (>10-15 countries) in multiple regions (NA, SA, APAC, MENA, Europe) is desirable
  • Experience leading concurrent multi-centered, multinational phase III clinical trials including project budget financial tracking and forecasting
  • Substantial experience in project supervision, mentoring and coaching project managers
  • Substantial experience with business development tasks, such as development of proposals, client presentations, bid defense meetings, and the like
  • Participation in mentoring and coaching of a representative number of project managers
  • Dermatology or rheumatology experience is required
  • Good knowledge of good clinical practices
  • Knowledge of applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines
  • PMP or PRINCE2 Certification is an asset
  • A Master’s degree is an asset

Benefits

Comp & perks
  • Flexible work schedule / work schedule
  • Home-based position
  • Ongoing learning and development
  • 401k
  • Benefits
  • Bonus structure plan
  • Attractive advancement opportunities