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
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Frank Scottile Blvd |Missouri :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
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Wavre |Tipperary :
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Netherlands |Remote Australia :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Bangkok |Israel :
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Kyiv |Lima Region :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
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