Senior Clinical Team Manager – HemOnc

Thermo Fisher Scientific

. Lead all clinical operational and quality aspects of allocated moderate- to high-complexity studies in compliance with ICH GCP .

Posted 11/10/2026full-timeRemote • South KoreaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in leading clinical trials, particularly in hematology and oncology, while ensuring compliance with ICH GCP and FDA guidelines. Proficient in managing clinical operations, mentoring teams, and implementing quality systems to achieve project deliverables.

Highest-signal resume keywords

Clinical Trial ManagementHematology And Oncology ExpertiseICH/GCP ComplianceLeadership And MentoringBudgeting And Financial Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData Quality PlansTrial Master File ManagementCRF DesignMonitoring PlansRegulatory SubmissionsClinical Monitoring PracticesProject Performance MetricsRisk ManagementForecasting

Soft Skills

LeadershipMentoringProblem-SolvingCommunicationOrganizational Skills

Tools & Technologies

OutlookExcelWordComputerized Applications

Industry Keywords

Clinical OperationsClinical Study ManagerEthics CommitteePatient ParticipationStudy Protocols

About the role

Key responsibilities & impact

Lead all clinical operational and quality aspects of allocated moderate- to high-complexity studies in compliance with ICH GCP
Implement and manage clinical aspects of trials from launch to closeout
Coordinate Clinical Management members allocated to projects on a regional or country basis
Partner with Project Managers on training, tracking, quality systems, timelines, budgets, and clinical deliverables
Act as the primary contact and support for project sponsors on clinical aspects
Develop clinical tools such as Monitoring Plans and Monitoring Guidelines
Contribute to Data Quality Plans and Master Action Plans
Set up, organize, maintain, and quality-check Trial Master File sections
Participate in designing CRFs, CRF guidelines, informed consent templates, and protocol-specific documents
Prepare, organize, and present at client, bid defense, and hand-off meetings
Collaborate with clinical and cross-functional teams to meet project deliverables
Lead team meetings and implement standardized clinical monitoring processes and training
Monitor clinical activity timelines, metrics, project performance, contractual obligations, and financials
Implement recovery actions, review monitoring visit reports, and lead CRF collection and query resolution
Communicate with study sites about protocols, patient participation, CRF completion, and study issues
Coordinate start-up activities and regulatory submissions when appropriate
Review and follow up on ethics committee questions
Provide clinical activity forecast estimates and manage clinical resources, assignments, and delegation
Mentor and train junior staff
Support process improvements, complex programs, regional leadership, Clinical Study Manager responsibilities, and project coordination as needed

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
8+ years of previous experience providing the knowledge, skills, and abilities to perform the job
Minimum of 8 years in clinical research
Track record of leading global clinical teams on hematology and oncology clinical trials
Equivalent combination of appropriate education, training and/or directly related experience may be considered
Advanced degree or equivalent experience in life sciences, medicine, or a related field preferred
Experience in preferred hematology and oncology therapeutic areas and indications
Strong leadership, mentoring, training, planning, organizational, interpersonal, problem-solving, judgment, decision-making, escalation, risk management, and communication skills
English language proficiency
Strong financial competence and knowledge of budgeting, forecasting and fiscal management
In-depth understanding of relevant regulations, including ICH/GCP and FDA guidelines
Comprehensive understanding of clinical monitoring practices, processes, and requirements
Strong computer skills using Outlook, Excel, Word, and computerized applications
Ability to independently lead clinical-only studies
Ability to communicate and understand information with diverse groups
Ability to work upright and stationary for typical working hours
Ability to work in non-traditional work environments
Ability to use and learn standard office equipment and technology
Ability to perform under pressure while prioritizing and handling multiple projects or activities
Ability to travel independently up to 20% by automobile, airplane, and train

Benefits

Comp & perks

Fully remote work arrangement
Standard Monday–Friday work schedule
Health and wellbeing support
Healthy and balanced work environment
Opportunities to work on innovative projects shaping global healthcare
Mentoring and training opportunities
Global and multicultural team collaboration