Clinical Team Manager – Senior

Thermo Fisher Scientific

Senior Clinical Team Manager managing clinical operational and quality aspects of studies. Working at Thermo Fisher Scientific to ensure clinical deliverables meet quality and timelines.

Posted 8/2/2026full-timeRemote • Texas • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical operations and quality aspects of studies, ensuring compliance with ICH GCP and FDA guidelines. Proficient in developing clinical tools, leading teams, and effectively communicating with stakeholders to achieve project deliverables.

Highest-signal resume keywords

Clinical Operations ManagementICH GCP ComplianceLeadership and Team IntegrationClinical Monitoring PracticesFinancial Acumen and Budget Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical MonitoringChange Management PrinciplesRegulatory ComplianceBudgeting and ForecastingRisk ManagementData Quality Plan DevelopmentMonitoring Plan DevelopmentPhase IV Studies ExperienceRWE Studies ExperienceStudy Site Communication

Soft Skills

Interpersonal SkillsProblem SolvingPlanning and Organizational SkillsAttention to DetailEffective Communication

Tools & Technologies

OutlookExcelWord

Industry Keywords

Clinical TrialsNon-Interventional StudiesMulticultural Matrix OrganizationStudy Start-Up ActivitiesContractual Deliverables

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage all clinical operational and quality aspects of allocated studies, of moderate to high complexity, in compliance with ICH GCP.
Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan.
Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
Collaborate with the clinical team and other departments as needed to meet deliverables of the project.
Responsible for the implementation and training of standardized clinical monitoring processes within the study.
Ensure achievement of the final clinical deliverable within the contractual time period specified.
Communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
May coordinate all start-up activities, and ensure that essential document quality meets the expectation of Regulatory Compliance Review.

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
Preferred experience: experience in STM role and/or previous experience in non-interventional / Phase IV studies / RWE studies.
Strong leadership skills, effective at mentoring and training, and capable of motivating and integrating teams.
Strong planning and organizational skills to enable effective prioritization of workload and workload of team members.
Strong interpersonal and problem solving skills to enable working in a multicultural matrix organization.
Solid understanding of change management principles.
Comprehensive understanding of the practices, processes, and requirements of clinical monitoring.
Strong judgment, decision making, escalation, and risk management skills.
Effective oral and written communication skills, including English language proficiency.
Capable of evaluating own and team members workload against project budget and adjust resources accordingly.
Strong financial acumen and knowledge of budgeting, forecasting and fiscal management.
Strong attention to detail.
In-depth understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
Strong computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
Capable of independently managing clinical only studies.

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work hours
Paid time off
Remote work options