Clinical Team Manager – HemOnc

Thermo Fisher Scientific

Clinical Trial Manager overseeing HemOnc clinical studies for Thermo Fisher Scientific, a global science-serving company. Managing trial deliverables, monitoring, regulatory documents, resources, and global clinical teams.

Posted 8/14/2026full-timeRemote • North Carolina • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial operations, ensuring compliance with ICH GCP and FDA guidelines, while effectively leading teams and coordinating resources to achieve project deliverables within timelines. Proficient in clinical monitoring practices, financial management, and communication with study sites to facilitate successful trial execution.

Highest-signal resume keywords

Clinical Trial OperationsICH GCP ComplianceGlobal CTM ExperienceFinancial ManagementLeadership and Team Integration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical MonitoringStudy ManagementData Quality PlansTrial Master File OrganizationCRF ManagementRegulatory SubmissionsBudgeting and ForecastingTherapeutic-Area KnowledgePatient-Care ResponsibilitiesDocument Quality Assurance

Soft Skills

Interpersonal SkillsProblem-Solving SkillsPlanning and Organizational SkillsJudgment and Decision-MakingEffective Communication

Tools & Technologies

OutlookExcelWordAutomated Applications

Industry Keywords

Clinical ResearchFSO/CRO ExperienceOvarian CancerSickle Cell DiseaseNon-Hodgkins LymphomaMultiple MyelomaCell and Gene TherapyCART-TRegulatory ComplianceEthics Committee Interaction

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage all clinical operational and quality aspects of allocated low- to moderate-complexity studies in compliance with ICH GCP
Develop clinical tools and contribute to Data Quality Plans, Master Action Plans, Trial Master File organization, CRFs, informed consent templates, and protocol-specific documents
Collaborate with project managers to prepare, organize, and present client meetings, including bid defense and hand-off meetings
Collaborate with clinical and other departments, lead team meetings, and maintain project timelines, resources, interactions, and quality
Implement and train standardized clinical monitoring processes
Ensure timely archiving of study documents and materials
Achieve final clinical deliverables within contractual timelines by monitoring clinical activity timelines and metrics, providing status updates, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution
Continuously monitor or co-monitor clinical trials to assess performance and meet contractual obligations
Conduct Accompanied Field Visits in smaller regions when applicable and manage project financials
Communicate with study sites regarding protocol, patient participation, case report forms, and other study issues
Coordinate study start-up activities and ethics committee and regulatory submissions when appropriate
Ensure essential document quality meets Regulatory Compliance Review expectations and follow up on ethics committee questions
Provide input into clinical activity forecasts
Manage clinical resources, delegate clinical responsibilities, and identify additional resource requirements

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic/vocational qualification
5+ years of relevant experience in clinical research, including clinical trial operations, study management, clinical monitoring, or related clinical research activities
Transferable healthcare, nursing, medicine, or related-discipline experience may be considered in combination with clinical trial experience when significant clinical expertise, therapeutic-area knowledge, and direct patient-care responsibilities are demonstrated
FSO/CRO experience required
Global CTM experience managing global teams required
Experience in one or more listed indications: Ovarian, Sickle Cell, Non-Hodgkins Lymphoma, Multiple Myeloma, Glioma, Head and Neck, Pancreas, Prostate, Non-Small Cell Lung, Breast, Colorectal, Radiopharmaceutical, Cell and Gene Therapy, and/or CART-T
Leadership, mentoring, training, team motivation, and team integration skills
Planning and organizational skills for workload prioritization
Interpersonal and problem-solving skills in a multicultural matrix organization
Ability to work effectively in changing environments with complex or ambiguous situations
Familiarity with clinical monitoring practices, processes, and requirements
Judgment and decision-making skills
Effective oral and written communication skills, including English language proficiency
Ability to evaluate workload against project budgets and adjust resources
Financial acumen and knowledge of budgeting, forecasting, and fiscal management
Strong attention to detail
Understanding of relevant regulations, including ICH/GCP and FDA guidelines
Computer skills using Outlook, Excel, Word, and other automated/computerized applications
Frequent domestic and international travel and driving to site locations

Benefits

Comp & perks

Collaboration and development as part of the everyday experience
Reasonable accommodation for individuals with disabilities during the application/interview process and employment
Equal opportunity employment