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Join to apply for the Clinical Trial Manager (Oncology) role at Medpace

Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.

Responsibilities

The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business.

Qualifications

• Bachelor’s degree in a health related field (Master’s degree or PhD is preferred);
• At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
• Experience in Oncology studies required;
• Excellent communication skills including good written and spoken English; and
• Flexible, accountable and comfortable in working in a global environment.
  
  

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
  
  

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
  
  

• Seniority level Not Applicable

• Employment type Full-time

• Job function Research, Analyst, and Information Technology
• Industries Pharmaceutical Manufacturing

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Queenstown, Central Singapore Community Development Council, Singapore 1 month ago

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Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.

The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business.

• Bachelor’s degree in a health related field (Master’s degree or PhD is preferred);
• At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
• Experience in Oncology studies required;
• Excellent communication skills including good written and spoken English; and
• Flexible, accountable and comfortable in working in a global environment.

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets

Job Summary
Medpace is currently looking for
Clinical Trial Manager (CTM)
to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.
Responsibilities
The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business.
Qualifications
Bachelor’s degree in a health related field (Master’s degree or PhD is preferred);
At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
Experience in Oncology studies required;
Excellent communication skills including good written and spoken English; and
Flexible, accountable and comfortable in working in a global environment.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
Medpace Perks
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
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• Conduct comprehensive health assessments and create personalized care plans
• Promote continuity of care through effective communication and teamwork
• Monitor and manage acute and chronic treatment toxicity
• Educate and support patients, families, and carers throughout the care process
• Advocate for patient rights, privacy, and informed consent
• Ensure accurate documentation in compliance with legal requirements
• Follow clinical protocols, including IV preparation and cannulation, for safe care

• Possess at least Diploma in Nursing
• At least 1 year of experience in oncology nursing
• Knowledge in radiation oncology is advantageous
• Must be an SNB registered Senior/ Staff Nurse

About Us

The National Cancer Centre Singapore (NCCS) is a leading national and regional tertiary cancer centre, attending to the majority of cancer cases in Singapore's public healthcare sector. We offer world class oncology care by having the best talent, doing robust clinical and translational research and leading education efforts to improve cancer outcomes. Join us to build a meaningful career and offer patients hope for a cancer-free tomorrow.

About the Role

The Executive in the Division of Radiation Oncology plays a crucial role in providing comprehensive secretarial and administrative support for the four Heads of Department. This includes handling various clerical tasks to ensure the smooth operation of the department and supporting medical staff in delivering high-quality patient care. Additionally, the executive serves as the primary point of contact for patients undergoing proton therapy, offering comprehensive administrative support to ensure a seamless patient experience from initial consultation to follow-up care. This involves close collaboration with medical staff, insurance companies, and patients to facilitate efficient and compassionate care throughout the process.

Some of the Key Responsibilities Include

• Manages schedules, documentation, and confidentiality for HODs, including meeting minutes, information dissemination, and database backups
• Organizes and maintains documents, provides executive assistance with project tasks, and coordinates with section leads to update policies and procedures
• Offers administrative support for new hires, collaborates with colleagues, and ensures coverage of duties when necessary
• Serve as the main point of contact for patients and their families, offering information, answering questions, and coordinating appointments for consultations, treatments, and follow-up visits
• Oversee patient records and documentation in the EMR system, assist with insurance claims, pre-authorizations, and the distribution of patient information materials
• Coordinate multidisciplinary team meetings, collaborate with healthcare professionals to ensure continuity of care, and monitor patient progress while following up on necessary interventions
• Provide assistance to patients in understanding their insurance benefits and financial responsibilities, and collaborate with the billing department to address any billing issues or discrepancies

Job Requirements

• Degree in any discipline with at least 2 years of relevant experience
• Experience in healthcare administrative role will be an added advantage
• Excellent communication and interpersonal skills.
• Strong organizational and multitasking abilities.
• Compassionate and patient-centered approach to care.
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Knowledge of medical terminology and healthcare procedures is an advantage.
• Familiarity with electronic medical records (EMR) systems.
• Strong problem-solving skills and the ability to anticipate needs

Job Opportunity

• Build and maintain strong scientific relationships with oncologists, hematologists, and pathologists
• Provide expert clinical and scientific education on precision oncology solutions, including applications in MRD, MCED, and therapy selection
• Support regional KOL engagement, advisory boards, and educational initiatives
• Collaborate cross-functionally with Medical, Clinical, Commercial, and Product teams to inform strategy
• Communicate field insights and emerging trends to internal stakeholders
• Represent us at conferences and support clinical studies, including investigator-led research and real-world data

• MD, PhD, or PharmD strongly preferred in oncology, molecular biology, genetics, or a related field
• Minimum 2 years' experience in Medical Affairs, MSL, or a clinical/scientific role in oncology or diagnostics
• Expertise in NGS, liquid biopsy, and the clinical application of molecular testing
• Familiarity with MRD and MCED technologies and their clinical adoption
• Skilled at presenting complex data to HCPs and cross-functional teams
• Knowledge of Singapore and APAC healthcare systems, with ability to support U.S. engagements
• Strong communication, collaboration, and relationship-building skills
• Willingness to travel (~30-40%) across APAC and occasionally to the U.S.

About us, we're advancing cancer care through precision oncology. Our work spans treatment selection, minimal residual disease (MRD), and multi-cancer early detection (MCED). We deliver clinically actionable insights through next-generation sequencing (NGS) and liquid biopsy technology.

We are seeking a Senior Medical Science Liaison to engage healthcare professionals across oncology and hematology. You'll support the appropriate use of our NGS-based clinical assays.

Key Responsibilities:

• Establish and maintain scientific relationships with oncologists, hematologists, and pathologists
• Provide clinical and scientific education on our precision oncology solutions
• Support regional Key Opinion Leader engagement, advisory boards, and educational initiatives
• Cross-functionally collaborate with Medical, Clinical, Commercial, and Product teams
• Communicate field insights and emerging trends to internal stakeholders
• Represent us at conferences and support clinical studies

Required Skills and Qualifications

• MD, PhD, or PharmD in oncology, molecular biology, genetics, or a related field
• Minimum 5 years' experience in Medical Affairs, MSL, or a clinical/scientific role in oncology or diagnostics
• Expertise in NGS, liquid biopsy, and molecular testing
• Familiarity with MRD and MCED technologies
• Knowledge of Singapore and APAC healthcare systems

Why Join Us?

Be part of a mission-driven team shaping personalized cancer care. At Lucence, you'll help bring precision diagnostics to more patients, so clinicians can make faster, informed decisions.