Clinical Trial Manager, Dermatology

Thermo Fisher Scientific

Clinical Trial Manager overseeing clinical studies with a focus on Atopic Dermatitis. Ensuring compliance with ICH GCP and delivering results within contractual timelines.

Posted 4/23/2026full-timeRemote • 🇸🇬 SingaporeMid-LevelSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP.
Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan.
Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central).
Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained.
Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics.
Continuously monitor or co-monitors clinical trials to assess performance and ensure contractual obligations are met.
Coordinate all start-up activities and ensure that timely ethics committee and regulatory submissions are addressed.
Review and follow up on all questions raised by the ethics committees.

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 5+ years).
Therapeutic experience in Atopic Dermatitis is essential to be considered for the opportunity.
Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams.
Good planning and organizational skills to enable effective prioritization of workload.
Familiarity with the practices, processes, and requirements of clinical monitoring.
Good computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
Capable of evaluating workload against project budget and adjusting resources accordingly.
Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.

Benefits

Comp & perks

Competitive salary
Health insurance
Professional development opportunities
Flexible working hours

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical operational managementquality assuranceclinical trial monitoringdata quality planningtrial master file managementclinical activity timeline preparationregulatory submissionsethics committee reviewperformance assessmentbudget evaluation

Soft Skills

leadershipmentoringteam integrationplanningorganizational skillseffective communicationprioritizationmotivationcollaborationpresentation skills

Certifications

Bachelor's degreeICH GCP certification