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Ctm - Atopic Dermatitis (Dermatology) Experience Required

3+ years
Not Disclosed
10 Nov. 13, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Trial Manager (CTM) – Atopic Dermatitis (Dermatology Experience Required)

📍 Location: Remote, North Carolina, USA
💼 Job ID: R-01329657
🕒 Job Type: Full-time
🏢 Category: Clinical Research
🌐 Remote: Fully Remote


About the Company

At Thermo Fisher Scientific, you’ll discover meaningful work that positively impacts global health.
Through our PPD® clinical research portfolio, we conduct clinical trials in over 100 countries — advancing drug development and enabling the delivery of life-changing therapies.

Our Clinical Operations teams provide end-to-end clinical trial support — from startup to closeout — helping clients reduce delays, optimize costs, and ensure top-quality outcomes.


About PPD Functional Service Provider (FSP) Solution

Our PPD FSP division partners with clients as an extension of their teams, providing:

  • Full-service clinical operations support

  • Consistent high-quality talent and training

  • Efficient capacity management and operational excellence

Joining the FSP group gives you the advantage of PPD’s CRO expertise while gaining dedicated client-side experience.


Position Summary

The Clinical Trial Lead (CTL) acts as a cross-functional global leader responsible for all operational deliverables from protocol development to study closeout.
This role requires strong dermatology (Atopic Dermatitis) experience, strategic oversight, and proven ability to lead global trials efficiently within timelines, budget, and quality standards.


Key Responsibilities

Clinical Trial Leadership

  • Lead all global operational aspects of clinical studies from Final Protocol Concept Sheet to Clinical Study Report (CSR).

  • Define and oversee trial timelines, budgets, milestones, and deliverables.

  • Ensure compliance with SOPs, ICH-GCP, and regulatory requirements.

  • Oversee and manage CROs, vendors, and cross-functional teams to meet contractual obligations.

  • Develop and maintain study-specific clinical documents (e.g., Monitoring Plans, Guidelines, Data Quality Plans).

Operational Excellence

  • Lead and mentor clinical teams, ensuring productivity, compliance, and alignment with project goals.

  • Track project progress using management tools and implement recovery or mitigation plans as needed.

  • Conduct or co-monitor clinical trials to assess performance and ensure deliverables are met.

  • Coordinate start-up activities (EC/regulatory submissions, ethics committee communications).

  • Ensure Trial Master File (TMF) completeness and document quality compliance.

Stakeholder Collaboration

  • Collaborate with Project Managers, Data Management, Biostatistics, and Regulatory teams.

  • Participate in client meetings, bid defenses, and kick-off sessions.

  • Communicate effectively with study sites regarding protocol adherence, data queries, and patient participation.

Financial & Resource Management

  • Support budget forecasting, resource allocation, and clinical cost tracking.

  • Evaluate workload vs. project budget and adjust resourcing as necessary.


Qualifications

Education

  • Bachelor’s degree (life sciences or equivalent).

  • Equivalent combination of education, training, and relevant experience may be accepted.

Experience

  • Minimum 3+ years of experience in clinical trial operations or site monitoring.

  • Strong background in Dermatology, specifically Atopic Dermatitis studies.

  • Prior experience in CRO, biotech, or pharmaceutical settings preferred.


Knowledge, Skills & Abilities

  • Proven leadership and team management skills.

  • Strong organizational, planning, and prioritization abilities.

  • Excellent communication and interpersonal skills.

  • Proficiency in Microsoft Office tools (Word, Excel, Outlook).

  • Sound financial acumen and understanding of budgeting and forecasting.

  • Comprehensive knowledge of ICH-GCP, FDA, and EMA guidelines.

  • Ability to adapt to complex and evolving environments.

  • Detail-oriented with excellent decision-making and problem-solving capabilities.

  • Fluent in spoken and written English.

  • Willingness to travel 10–20% domestically and internationally.


Work Schedule

  • Standard (Monday – Friday)

Work Environment

  • Office or home-based (remote setup)

  • Requires extended screen time, document handling, and occasional travel.


Why Join Thermo Fisher Scientific

  • Competitive compensation and performance bonuses

  • Comprehensive healthcare and employee benefits

  • Strong focus on career development and training

  • Work culture built on Integrity, Intensity, Innovation, and Involvement