What Jobs are available for Clinical Assistant in Malaysia?

Nurse, Medical Assistant & Clinical Assistant

We are seeking a talented and dedicated Nurse, Medical Assistant & Clinical Assistant to join our team at POLIKLINIK SHAIK SDN. BHD. in Kota Kemuning, Selangor. This full-time position is a crucial role within our organisation, supporting our mission to provide high-quality medical care to our patients. What you'll be doing

Providing nursing care and assistance to patients, including administering medication, monitoring vital signs, and assisting with daily living activities Collaborating with physicians and other healthcare professionals to develop and implement patient treatment plans Maintaining accurate and detailed patient records and documentation Assisting with medical procedures, such as minor surgeries and diagnostic tests Ensuring a clean, safe, and well-stocked clinical environment Providing excellent customer service and support to patients and their families What we’re looking for

Registered nurse or medical assistant qualification, with a minimum of 1-2 years of experience in a similar role Strong clinical skills and knowledge of nursing practices and procedures Excellent communication and interpersonal abilities, with a patient-centred approach Ability to work well in a team and under pressure Proficient in using medical equipment and technology Commitment to continuing professional development and staying up-to-date with industry best practices What we offer

At POLIKLINIK SHAIK SDN. BHD., we are committed to providing our employees with a supportive and rewarding work environment. We offer competitive salaries, opportunities for career advancement, and a range of benefits, including comprehensive health insurance and a generous leave policy. About us

POLIKLINIK SHAIK SDN. BHD. is a leading provider of healthcare services in the Kota Kemuning region. Our mission is to deliver exceptional, patient-centred care that improves the health and well-being of our community. We are a dynamic and growing organisation, with a strong focus on innovation and continuous improvement.

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Patient Care Assistant

MAHSA Specialist Hospital is seeking caring and dedicated Patient Care Assistants to join our nursing team. As a Patient Care Assistant, you will play an integral role in providing essential care and support to our patients. Key Responsibilities: Assist patients with daily living activities, such as bathing, dressing, and eating Monitor and record vital signs and report any changes to the nursing staff Assist in patient mobility and transfer Maintain a clean and safe patient environment Provide emotional support and companionship to patients Qualifications: Certificate or diploma in Nursing or Healthcare Assistance Previous experience as a Patient Care Assistant or Nursing Assistant is a plus Strong communication and interpersonal skills Empathetic and patientfocused with a caring attitude Willingness to work in shifts, including nights and weekends Join our compassionate nursing team at MAHSA Specialist Hospital as a Patient Care Assistant. Apply now and be a part of our mission to provide excellent patient care and support.

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Position Overview We are looking for compassionate and committed healthcare professionals including Registered Nurses, Healthcare Assistants, or Medical Assistants to join our Lucenxia Patient Care Team. The role focuses on supporting patients using Lucenxia PD systems, coordinating with hospital PD units, and ensuring safe, high‑quality care delivery.

Key Responsibilities

Manage and support patients on Lucenxia Peritoneal Dialysis systems.

Conduct home visits for assessments, training, and follow‑up care.

Monitor and report patient well‑being and clinical outcomes.

Collaborate with hospital PD Unit teams, doctors, and nephrologists.

Recruit and assist new patients referred for Peritoneal Dialysis.

Support PD machine installation, inventory checks, and emergency deliveries.

Maintain accurate documentation and reports via electronic systems.

Participate in patient education and awareness activities.

Provide training or assist in training when required.

Perform other tasks as assigned by supervisors or management.

Requirements

Registered Nurse (RN) with valid APC, or qualified Healthcare Assistant / Medical Assistant.

Fresh graduates are welcome; training and support will be provided.

Strong interest in renal care, home‑based nursing, or community health.

Good communication and interpersonal skills.

Must possess own transport and be willing to travel.

Able to work independently, responsibly, and with compassion.

About Lucenxia (M) Sdn Bhd Lucenxia (M) Sdn Bhd started its operation in Malaysia in 2011 with a vision to provide the best and most affordable home dialysis care treatment for renal patients. Lucenxia is associated with Lucenxia Prescience AG, a Swiss company at the forefront of dialysis technology. It is part of an international group of dialysis service providers. Since then, the company has expanded to all states, including Sabah & Sarawak.

To achieve this, we introduced the Automated Peritoneal Dialysis equipment called the Intellis. The Intellis is designed to make home dialysis treatment simple, easy and allows treatment at almost any home in the country. As a night treatment, this option minimizes any daytime disruptions to daily life, working or retirement.

Our team is trained to care for and assist dialysis patients in their treatment and to extend help whenever possible to their caregivers. We believe dialysis is not just a clinical treatment but a long‑term care program that can help a patient lead a better life. We strategically locate our team of experienced patient‑care nurses, clinicians and technical specialists to care for our patients and their needs 24 hours a day.

Driving this is the Innovation Team of clinicians and specialists working closely with our global teams to continuously research and develop new options that can enhance the quality of life for our patients.

As part of our continuous expansion in Malaysia and overseas, we have challenging careers for proactive candidates. If you are ambitious, aggressive and willing to go the extra mile to succeed, we would like to invite you to join our team.

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JR Clinical Associate
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
**What you will be doing**
+ Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
+ Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
+ Support the preparation of study-related materials, such as informed consent forms and case report forms.
+ Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
+ Contribute to the tracking and reporting of clinical trial metrics and milestones.
**Your profile**
+ Bachelor's degree in a scientific or healthcare-related field.
+ Prior experience or strong interest in clinical research.
+ KNwledge of clinical trial processes, regulations, and guidelines.
+ Excellent organizational and communication skills.
+ Ability to work collaboratively in a fast-paced environment with attention to detail.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

JR Clinical Associate

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

Support the preparation of study-related materials, such as informed consent forms and case report forms.

Work with cross-functional teams to facilitate communication and ensure smooth trial execution.

Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your profile

Bachelor's degree in a scientific or healthcare-related field.

Prior experience or strong interest in clinical research.

KNwledge of clinical trial processes, regulations, and guidelines.

Excellent organizational and communication skills.

Ability to work collaboratively in a fast-paced environment with attention to detail.

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

Life assurance

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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JR Clinical Associate

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

Support the preparation of study-related materials, such as informed consent forms and case report forms.

Work with cross‑functional teams to facilitate communication and ensure smooth trial execution.

Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your profile

Bachelor's degree in a scientific or healthcare‑related field.

Prior experience or strong interest in clinical research.

KNwledge of clinical trial processes, regulations, and guidelines.

Excellent organizational and communication skills.

Ability to work collaboratively in a fast‑paced environment with attention to detail.

What ICON can offer you Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work life balance opportunities for you and your family.

Our benefits examples include

Various annual leave entitlements

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.

Life assurance

Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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JR Clinical Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What You Will Be Doing

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

Support the preparation of study-related materials, such as informed consent forms and case report forms.

Work with cross-functional teams to facilitate communication and ensure smooth trial execution.

Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your Profile

Bachelor's degree in a scientific or healthcare-related field.

Prior experience or strong interest in clinical research.

Knowledge of clinical trial processes, regulations, and guidelines.

Excellent organizational and communication skills.

Ability to work collaboratively in a fast-paced environment with attention to detail.

What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include

Various annual leave entitlements

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

Life assurance

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply.

Seniority level Entry level

Employment type Full-time

Job function Research, Analyst, and Information Technology

Industries Pharmaceutical Manufacturing

Location: Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia

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JR Clinical Associate

ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

Support the preparation of study‑related materials, such as informed consent forms and case report forms.

Work with cross‑functional teams to facilitate communication and ensure smooth trial execution.

Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your profile

Bachelor’s degree in a scientific or healthcare‑related field.

Prior experience or strong interest in clinical research.

Knowledge of clinical trial processes, regulations, and guidelines.

Excellent organizational and communication skills.

Ability to work collaboratively in a fast‑paced environment with attention to detail.

What ICON can offer you: In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.

Various annual leave entitlements.

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well‑being.

Life assurance.

Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply.

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Clinical Technical Support Specialist page is loaded Clinical Technical Support Specialist Apply locations Thailand Pakistan Kuala Lumpur Vietnam Indonesia time type Full time posted on Posted 2 Days Ago job requisition id R-

Please submit your application as soon as possible, as we reserve the right to close this advertisement at any time.

Cochlear is the global market leader in implant hearing solutions. Cochlear's mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear Implant is an electronic device that is surgically implanted under the skin near the ear that restores hearing to those who suffer from severe hearing loss. It’s an incredible piece of engineering and the only product in the world that restores a sense through technology. Imagine using your experience to help people around the world to hear again. We can offer a unique opportunity to join Cochlear, an iconic Australian company, leading the world in implantable hearing solutions. Our mission is to help more people to hear. Job Overview & Purpose The Clinical Technical Support Specialist role is responsible for ensuring clinical excellence in everyday cochlear implant management and clinical operations across AGM countries, primarily in Pakistan and Sri Lanka. This role conducts comprehensive training sessions for distributor teams, ensuring strict adherence to established clinical and technical protocols, offering both clinical and technical support throughout the implant lifecycle—from candidacy evaluation through post-operative care. It is tasked with remotely providing support and troubleshooting clinical issues, managing escalated clinical and technical concerns, and supporting integrity tests. In addition, the role support country teams in complaints processes and collaborates with clinical leadership to continuously update and implement training materials and clinical protocols. This is a remote position with the requirement to travel for on-site training sessions and direct distributor engagements regularly preferably based out of Thailand. Accountabilities

Accountability 1 Develops and maintains tools and training materials to assist field teams with troubleshooting and management of cases. Conducts and performs product integrity tests for difficult case management in countries. Key Responsibilities: Clinical & Technical Support: Provide clinical support for cochlear implant management, including candidacy evaluations, surgical preparation, and post-operative care. Troubleshoot clinical technical issues remotely, guiding distributors through problem resolution. Assist with complaints management by accurately documenting issues and contributing to root cause analyses. Serve as the primary contact for handling escalated clinical issues, ensuring timely and effective resolution. Coordinate with the customer services team to maintain consistency and excellence in service delivery. Support integrity testing processes. Training & Education:

Deliver regular training sessions to distributor audiologists/mapping clinicians, ensuring they are well-versed in both the clinical aspects of cochlear implants and Cochlear’s product portfolio. Work with the AGM Clinical Affairs Manager and APAC Clinical to develop and update training materials and protocols to support distributor education. Team Job

Individual contributor: Work safely, complying with all safety procedures, rules, and instructions; and reporting workplace hazards, incidents, or injuries to manager.

Minimum Key Incumbent Requirements

Required Skills Proven experience in clinical technical support and troubleshooting within the cochlear implant or related healthcare field is an asset.

Solid understanding of cochlear implant technology and clinical protocols—from initial candidacy assessments to post-operative support.

Familiarity with troubleshooting clinical equipment and implant-related software.

Strong ability to meet tight timelines and manage high-demand situations effectively.

Advanced analytical skills with keen attention to detail, along with excellent problem-solving and case management abilities.

Ability to follow established protocols and enforce requirements effectively. Excellent communication skills, with the ability to explain complex

technical information clearly and concisely.

Demonstrated problem-solving capabilities and a proactive approach to addressing challenges.

Familiarity with Cochlear’s implant portfolio is a bonus.

Candidates must have no travel restrictions to Asia Growth Market countries (including Pakistan and Sri Lanka)

Education Bachelor of Audiology or above Languages English - Fluent (Required) Urdu - Fluent (Preferred) Work Experience 3 years hands-on experience managing cochlear implant patients preferred. Previous experience in customer support or technical support roles is a bonus. Cochlear’s mission is to help people hear and be heard. As the global leader in implantable hearing solutions, Cochlear is dedicated to helping people with moderate to profound hearing loss experience a life full of hearing. We aim to give people the best lifelong hearing experience and access to innovative future technologies. We collaborate with the industry’s best clinical, research and support networks. That’s why more people choose Cochlear than any other hearing implant company. Learn and grow with us as we tackle the most complex challenges in helping more people to hear and experience life’s opportunities. If you feel that you have the skills and experience to be successful in this role and take on new challenges to build your career with Cochlear, please start your application by clicking the apply button below. #CochlearCareers How we recognise your contribution We want Cochlear to be a place where our people truly enjoy coming to work. Through our internal programs and employee benefits, we aim to create an environment where our people will feel value and supported. Whether your focus is on continuous learning, professional development or simply finding an environment which enables you to thrive whilst balancing family or personal life commitments, then we have several programs in place to support you. For more information about Life at Cochlear, visit At Cochlear we value and welcome the unique contributions, perspectives, experiences, and backgrounds of our employees and aim to build a culture that celebrates and leverages these differences, creating a sense of belonging and enabling our people to realise their full potential. We offer flexible working arrangements, and we understand flexibility is not the same for everyone. We're open to a conversation about what flexibility means for you.

Welcome!

Our growth is creating great opportunities! Our team is expanding and we want to hire the most talented people we can. Continued success depends on it. So once you've had a chance to explore our current open positions, apply to the ones you feel suit you best and keep track of both your progress in the selection process, and new postings that might interest you! We're the global leader in implantable hearing solutions. We have provided more than 600,000 implantable devices, helping people of all ages to lead full and active lives. Our Mission

We help people hear and be heard. We empower people to connect with others and live a full life. We help transform the way people understand and treat hearing loss. We innovate and bring to market a range of implantable hearing solutions that deliver a lifetime of hearing outcomes.

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