Senior Project Manager – Dermatology/Rheumatology

Innovaderm Research Inc.

. Serve as the primary contact for the Sponsor .

Posted 9/15/2026full-timeRemote • IrelandSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates extensive experience in global clinical project management, including oversight of all project phases, vendor management, and budget control. Proficient in ensuring compliance with GCP and ICH standards while effectively leading cross-functional teams to deliver high-quality study outcomes.

Highest-signal resume keywords

Global Clinical Project ManagementMultinational Phase III Clinical TrialsPMP or PRINCE2 CertificationGCP and ICH Standards KnowledgeBudget Financial Tracking and Forecasting

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 Protocol DevelopmentECRF PreparationQuality Assurance Audit ReviewRisk ManagementStudy Start-UpRegulatory SubmissionData ManagementMedical WritingVendor ManagementRecruitment Management

Soft Skills

Effective CommunicationProblem-Solving AbilitiesTeam CollaborationRelationship BuildingAbility to Work Under Pressure

Tools & Technologies

Microsoft Office Suite

Certifications & Qualifications

PMPPRINCE2

Industry Keywords

Clinical ResearchCRODermatology TrialsOncology TrialsRegulatory Affairs

Tech Stack

Tools & technologies

Google Cloud PlatformPMP

About the role

Key responsibilities & impact

Serve as the primary contact for the Sponsor
Provide efficient and timely updates on trial progress
Lead client calls effectively
Oversee and actively participate in preparing study plans, protocols, informed consent forms, eCRFs, TLFs, and clinical study reports
Participate in planning and conducting Investigator Meetings
Ensure each site has the necessary materials, investigational products, supplies, equipment, and safety lab kits
Ensure assigned studies are audit ready at all times
Monitor the quality of study deliverables, including vendor and SubCRO deliverables, and address issues
Manage risks and control measures to assure project quality
Analyze discrepancies between planned and actual results
Review and approve responses to quality assurance audits
Control project budgets, including internal hours allocated to activities
Identify out-of-scope activities for change orders
Proactively manage trial timelines, budgets, resources, and vendors
Coordinate tasks and deliverables across functional departments
Communicate with study team members, functional departments, and senior management
Manage and report recruitment status and identify initiatives needed to meet recruitment timelines
Lead the core project team, including Associate Project Managers, Project Coordinators, and Project Assistants
Ensure all team members receive adequate project training
Collaborate with Site Selection, Regulatory Affairs, Data Management, Clinical Monitoring, Biostatistics, and Scientific Affairs teams and vendors to complete deliverables on time and according to applicable standards

Requirements

What you’ll need

At least 7 years of global clinical project management experience, including management of all project phases from start-up to closure, all functional services, and vendor management
At least 10 years of industry experience, including a minimum of 3 years in a CRO
Experience with mid-size and large studies involving more than 10–15 countries across multiple regions (NA, SA, APAC, MENA, Europe)
Experience leading multicentered, multinational Phase III clinical trials, including project budget financial tracking and forecasting
B.Sc. in a related field of study to clinical research
PMP or PRINCE2 certification is an asset
Experience in study start-up, regulatory submission, resource management, supervisory experience, CRA, data management, medical writing, or vendor management is an asset
Therapeutic experience managing dermatology, onco-dermatology, rheumatoid arthritis, or oncology trials is an asset
Excellent knowledge of GCP and ICH standards and local country regulations
Excellent knowledge of Microsoft Office suite
Fluency in English with excellent oral and written skills is required
Bilingualism in English and the local language is an asset
Ability to work in a team environment and establish good relationships with colleagues and sponsors
Good problem-solving abilities
Strong ability to carry out different projects and work under pressure while meeting timelines

Benefits

Comp & perks

Flexible schedule
Vacation
Home-based position
Ongoing learning and development opportunities
Attractive opportunities for growth and advancement