24 Radiation Therapists jobs in Singapore

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

Join to apply for the Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology) role at Medpace

Join to apply for the Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology) role at Medpace

Get AI-powered advice on this job and more exclusive features.

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

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 radiopharmaceuticals . 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
• Coordinate project meetings and produce quality minutes
  
  

• PhD in Life Sciences (nuclear medicine/ radiopharmaceuticals/ radiation oncology or related)
• 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
  
  

• 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

Referrals increase your chances of interviewing at Medpace by 2x

Get notified about new Clinical Trial Manager jobs in Singapore, Singapore .

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

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

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 radiopharmaceuticals . 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).

• 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
• Coordinate project meetings and produce quality minutes

• PhD in Life Sciences (nuclear medicine/ radiopharmaceuticals/ radiation oncology or related)
• 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

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

Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)
Join to apply for the
Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)
role at
Medpace
Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)
Join to apply for the
Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)
role at
Medpace
Get AI-powered advice on this job and more exclusive features.
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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 radiopharmaceuticals . 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
Coordinate project meetings and produce quality minutes
Qualifications
PhD in Life Sciences (nuclear medicine/ radiopharmaceuticals/ radiation oncology or related)
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
Medpace Overview
Medpace is a full-service clinical contract research organisation (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.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
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.
Seniority level
Seniority level Not Applicable
Employment type
Employment type Full-time
Job function
Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Medpace by 2x
Get notified about new Clinical Trial Manager jobs in
Singapore, Singapore .
Associate Clinical Trial Manager - PhD / Post-Doc - Infectious Disease
Asst Manager/Manager, Clinical Research & Innovation Office
Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)
Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM))
Associate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (CVRM))
Research Associate (Clinical Healthy Longevity Trials)
Queenstown, Central Singapore Community Development Council, Singapore 1 month ago
Associate Clinical Research Coordinator, Ophthalmology
Clinical Research Associate / Senior Clinical Research Associate
Clinical Research Associate / Senior Clinical Research Associate
Project Coordinator (Senior Executive/ Asst Manager), Clinical Service Planning
Senior Lead Clinical Research Associate, Research Compliance Management
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Job Summary
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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 radiopharmaceuticals . 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
Coordinate project meetings and produce quality minutes
Qualifications
PhD in Life Sciences (nuclear medicine/ radiopharmaceuticals/ radiation oncology or related)
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
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
#J-18808-Ljbffr

Job Scope:

• Plan and deliver accurate radiation treatments as prescribed by the Radiation Oncologist.
• Perform CT simulations, treatment device setup, and dosimetry calculations.
• Operate radiation therapy equipment in line with SOPs and safety protocols.
• Conduct equipment quality assurance checks.
• Maintain accurate treatment records and documentation.
• Ensure high standards of patient care and manage treatment side effects.
• Carry out additional tasks as assigned by the supervisor.

Job Requirements:

• Bachelor's Degree in Medical Radiation Technology or related field.
• Competent in clinical radiation therapy, including pre-treatment and treatment delivery.
• Knowledge of radiation safety, QA procedures, and infection control.

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button

We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities.

"JobStudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties, please be aware of scams impersonating JobStudio and our employees. You may call our office directly for verification. We will not be liable for loss arising from scams."

JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Esther

EA Personnel Reg No: R

• Competitive Remuneration Package
• Accessible Working Location, Close Proximity to MRT
• Office Hours

As a Radiation Therapist (Various Setting), you will be responsible for the following duties:

• To perform CT-simulation, treatment device construction, dosimetry calculation for the delivery of radiation treatment based on department treatment protocol and plan approved by the Radiation Oncologist.
• To operate radiation therapy machine and other supportive equipment in accordance with the department standard operation protocols and radiation safety practice.
• To adhere to safe radiation practices, occupational health hazards prevention and infection control precautions.
• To perform quality assurance check on radiation therapy equipment to ensure proper operation, policies, and protocols of patient care.
• To maintain accurate record and documentation of radiation dose delivered to patient.
• To maintain high standards of patient care, clinical communication and the timely escalation of management of patients' side effects.
• To guide and mentor student Radiation Therapist assigned to unit.
• To participate in departmental / Radiation Therapists' professional development, education and research activities.
• To assume additional responsibilities assigned by supervisor.

Requirements:

• Must have a Degree in Radiation Therapy or any related qualification from recognized institutions

To apply, simply click on the ''apply'' button in the job advertisement or alternatively, you can send in your resume via email.

Email Address: .COM.SG

We regret to inform that only shortlisted candidates will be notified.

ALLIED SEARCH PTE. LTD.

EA LICENSE : 19C9777

Job Scope:

• Responsible for coordinating, planning and administering accurate radiation treatment to patient.
• To perform CT-simulation, treatment device construction, dosimetry calculation for the delivery of radiation treatment based on department treatment protocol and plan approved by the Radiation Oncologist.
• To operate radiation therapy machine and other equipment in accordance with the SOP and radiation safety practice.
• To adhere to safe radiation practices, occupational health hazards prevention and infection control precautions.
• To perform quality assurance check on radiation therapy equipment to ensure proper operation, policies, and protocols of patient care.
• Responsible for data record and documentation of radiation dose delivered to patient.
• To maintain high standards of patient care, clinical communication and the timely escalation of management of patients' side effects.
• To assume additional responsibilities assigned by supervisor.

Job Requirements:

• Bachelor Degree in Medical Radiation Technology or related fields.
• Competent in clinical radiation therapy to perform pre-treatment and treatment delivery procedures to patient.

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button

We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities.

"Jobstudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties, please be aware of scams impersonating Jobstudio and our employees, you may call our office directly at for verification. we will not be liable for loss arising from scams."

JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Choong Yi Han

EA Personnel Reg No: R

• Competitive Remuneration Package
• Accessible Working Location, Close Proximity to MRT
• Office Hours

As a Radiation Therapist, you will be responsible for the following duties:

• To perform CT-simulation, treatment device construction, dosimetry calculation for the delivery of radiation treatment based on department treatment protocol and plan approved by the Radiation Oncologist.
• To operate radiation therapy machine and other supportive equipment in accordance with the department standard operation protocols and radiation safety practice.
• To adhere to safe radiation practices, occupational health hazards prevention and infection control precautions.
• To perform quality assurance check on radiation therapy equipment to ensure proper operation, policies, and protocols of patient care.
• To maintain accurate record and documentation of radiation dose delivered to patient.
• To maintain high standards of patient care, clinical communication and the timely escalation of management of patients' side effects.
• To guide and mentor student Radiation Therapist assigned to unit.
• To participate in departmental / Radiation Therapists' professional development, education and research activities.
• To assume additional responsibilities assigned by supervisor.

Requirements:

• Must have a Degree in Radiation Therapy or any related qualification from recognized institutions

To apply, simply click on the ''apply'' button in the job advertisement or alternatively, you can send in your resume via email.

Email Address: .COM.SG

We regret to inform that only shortlisted candidates will be notified.

ALLIED SEARCH PTE. LTD.

EA LICENSE : 19C9777