Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)

Medpace; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a full-time Associate Clinical Trial Manager to join their Clinical Trial Management team in Singapore. This role is perfect for recent PhD graduates looking to transition into the biotech industry. You will receive comprehensive training and work in a dynamic international environment, supporting project coordinators and clinical trial managers. Responsibilities include managing project timelines, ensuring quality control, and collaborating with various stakeholders. If you're eager to apply your academic skills in a practical setting and pursue a fast-tracked career in clinical trial management, this opportunity is for you.

Qualifications

• PhD in Life Sciences required with a focus on Oncology preferred.
• Strong communication and organizational skills are essential.

Responsibilities

• Collaborate on global study activities with project teams.
• Ensure timely delivery of tasks with high accuracy.

Skills

Analytical Skills

Communication Skills

Organizational Skills

Presentation Skills

Education

PhD in Life Sciences

Tools

Microsoft Excel

Word Processing Software

Databases

Job description

Job Summary

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Singapore office. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports within the clinical trial management system;
• Interact with the internal project team, Sponsor, study sites, and third-party vendors;
• Provide oversight and quality control of our internal regulatory filing system;
• Provide oversight and management of study supplies;
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality minutes.

Qualifications

• PhD in Life Sciences;
• Experienced in Oncology;
• Fluency in English with solid presentation skills;
• Ability to work in a fast-paced dynamic industry within an international team;
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
• Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.