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
Work Model: Fully Remote
About the Role
Thermo Fisher Scientific’s PPD® clinical research services are advancing global healthcare by driving excellence in clinical trial delivery. Our Clinical Operations teams support end-to-end clinical development across more than 100 countries, contributing directly to the creation of innovative, life-changing therapies.
We are seeking an experienced Clinical Trial Manager (CTM) with mandatory experience in Atopic Dermatitis/Dermatology clinical studies. This global leadership role oversees operational delivery of Phase I–IV clinical trials, ensuring quality, compliance, and execution excellence.
As part of the PPD Functional Service Provider (FSP) model, you will work as a client-dedicated professional while being fully integrated into our CRO network, benefiting from best-in-class support, training, and technology.
Position Overview
The CTM provides cross-functional leadership, operational direction, and strategic insight to ensure seamless trial delivery from protocol development to Clinical Study Report (CSR) completion. This role is suited for clinical research professionals with strong experience in dermatology trials, complex global operations, vendor oversight, and team leadership.
Key Responsibilities
Clinical Trial Leadership
Lead global clinical studies ensuring delivery within agreed timelines, budgets, quality standards, SOPs, and regulatory requirements.
Establish, review, and refine study timelines and budgets using internal and external benchmarks.
Oversee full trial lifecycle including start-up, execution, monitoring, and study close-out.
Vendor & CRO Oversight
Direct CROs and external vendors to ensure adherence to contractual performance metrics.
Lead development of trial tools and study-specific guidelines including Monitoring Plans and Data Quality Plans.
Operational Excellence
Support Trial Master File (TMF) set-up, maintenance, and quality review.
Contribute to CRF and informed consent form development.
Drive team alignment through regular communication, meetings, and milestone tracking.
Regulatory & Compliance
Ensure essential document quality meets global regulatory expectations, including ICH-GCP and FDA guidelines.
Oversee site communication related to protocols, enrollment, data entry, and study conduct.
Coordinate ethics and regulatory submissions where required.
Resource & Financial Management
Evaluate workload against project budgets and allocate resources accordingly.
Monitor clinical performance metrics, implement corrective actions, and ensure compliance with project financials.
Cross-Functional Collaboration
Work closely with project managers for proposal development, client presentations, and bid defense meetings.
Collaborate across clinical operations, data management, medical monitoring, safety, and quality functions.
Experience Required
Minimum Experience
3+ years of experience in clinical research with proven ability to manage global clinical trials.
Mandatory experience in Atopic Dermatitis or Dermatology clinical studies.
Hands-on experience in site monitoring and clinical operations.
Experience managing cross-functional teams in a CRO or pharmaceutical environment.
Additional Requirements
Bachelor’s degree in life sciences or relevant field (or equivalent combination of education and experience).
Strong understanding of ICH-GCP, FDA standards, and international regulatory requirements.
Ability to lead, train, and mentor clinical team members.
Proficiency in trial management systems and standard office applications.
Strong organizational, analytical, and problem-solving abilities.
Excellent English communication skills.
Willingness to travel 10–20% as needed.
Key Skills & Competencies
Leadership and team integration capabilities.
Ability to thrive in dynamic, complex environments.
Budgeting, forecasting, and financial management understanding.
Attention to detail and strong documentation discipline.
Multicultural communication and stakeholder engagement skills.
Why Join Thermo Fisher Scientific?
Thermo Fisher Scientific offers competitive compensation, comprehensive benefits, professional development pathways, and a mission-driven culture focused on improving global health. Joining the PPD FSP model allows you to contribute to impactful clinical programs while gaining client-dedicated experience and access to world-class CRO resources.
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