About this role
The Associate Clinical Trial Manager will support Project Coordinators and Clinical Trial Managers in project management activities, ensuring timely delivery of tasks and maintaining project-specific status reports. They will also interact with internal teams, sponsors, study sites, and vendors, while overseeing regulatory filings and study supplies.
Candidates must have a PhD in Life Sciences and experience in Oncology, along with fluency in English and strong presentation skills. While prior experience in the CRO or pharmaceutical industry is advantageous, it is not required.
What they're looking for
Project ManagementCommunicationCollaborationOrganizational SkillsAnalytical SkillsPresentation SkillsRegulatory KnowledgeQuality Control
Frequently asked questions
What does a Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) at Medpace, Inc. do?
The Associate Clinical Trial Manager will support Project Coordinators and Clinical Trial Managers in project management activities, ensuring timely delivery of tasks and maintaining project-specific status reports. They will also interact with internal teams, sponsors, study sites, and vendors, whi…
What skills does this Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) role need?
Key skills for this role include Project Management, Communication, Collaboration, Organizational Skills, Analytical Skills, Presentation Skills.
How much does a Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) at Medpace, Inc. pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) role?
You can apply directly on Medpace, Inc.'s careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.