Clinical Team Manager

Thermo Fisher Scientific

. Manage clinical operational and quality aspects of allocated low- to moderate-complexity studies in compliance with ICH GCP .

Posted 9/16/2026full-timeRemote • Texas • United StatesMid-LevelSeniorWebsite

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 cross-functional teams and maintaining project timelines and quality. Proficient in clinical monitoring practices, financial management, and developing clinical tools and documentation.

Highest-signal resume keywords

Clinical Trial OperationsICH GCP ComplianceLeadership and MentoringFinancial ManagementClinical Monitoring Practices

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchStudy ManagementData Quality ManagementCRF DesignProject Financial ManagementRegulatory SubmissionsMonitoring Plans DevelopmentTrial Master File ManagementPatient Care ResponsibilitiesTherapeutic Area Knowledge

Soft Skills

Interpersonal SkillsProblem-Solving SkillsPlanning and Organizational SkillsEffective Communication SkillsJudgment and Decision-Making Skills

Tools & Technologies

OutlookExcelWord

Industry Keywords

FSO/CRO ExperienceGlobal CTM ExperienceOvarian CancerSickle Cell DiseaseNon-Hodgkins LymphomaMultiple MyelomaGliomaCell and Gene TherapyCAR-TClinical Monitoring Practices

About the role

Key responsibilities & impact

Manage clinical operational and quality aspects of allocated low- to moderate-complexity studies in compliance with ICH GCP
Assume Clinical Study Manager responsibilities on small or less complex projects when required
Develop clinical tools, monitoring plans, monitoring guidelines, and contribute to data quality and master action plans
Set up, organize, maintain, and archive relevant Trial Master File sections and study materials
Participate in designing CRFs, CRF guidelines, informed consent templates, and protocol-specific documents
Collaborate with project managers to prepare and present client meetings, including bid defense and hand-off meetings
Lead clinical team meetings and coordinate with clinical and cross-functional teams to maintain timelines, resources, quality, and interactions
Implement and train standardized clinical monitoring processes
Monitor clinical activity timelines and metrics, provide status updates, review projects and monitoring visit reports, implement recovery actions, and manage CRF collection and query resolution
Conduct or co-monitor clinical trials and assess performance against contractual obligations
Conduct Accompanied Field Visits and manage project financials in smaller regions when required
Communicate with study sites regarding protocols, patient participation, case report forms, and study issues
Coordinate study start-up activities and ethics committee and regulatory submissions when required
Review and follow up on ethics committee questions and ensure essential document quality
Provide input into clinical activity forecasts and manage clinical resources, responsibilities, delegation, and 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 experience in healthcare, nursing, medicine, or related disciplines may be considered in combination with clinical trial experience where the candidate demonstrates significant clinical expertise, therapeutic area knowledge, and direct patient care responsibilities
FSO/CRO experience
Global CTM experience managing global teams
Indication experience in 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 CAR-T
Leadership, mentoring, and training skills
Planning and organizational skills
Interpersonal and problem-solving skills
Ability to work in multicultural matrix organizations and 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 budget and adjust resources
Financial acumen and knowledge of budgeting, forecasting, and fiscal management
Strong attention to detail
Understanding of ICH/GCP and FDA guidelines
Good computer skills, including Outlook, Excel, and Word
Frequent domestic and international travel and driving to site locations

Benefits

Comp & perks

Global team environment
Collaboration and development opportunities
Scientific excellence-focused workplace
Domestic and international travel opportunities