663 Medical Research Assistant jobs in Singapore

Medical Research Assistant (Govt Hospital)

Location: Queenstown

Working Hours: Mon-Fri, 8.00am-4.30pm

Saturdays, 8.00am - 12.30pm

Duration: 6 Months Renewable contract

Salary: Up to $3400

Benefits:

• Government Hospital - Stable industry
• AWS + 2-3 months performance bonus + yearly salary increment
• Good leave policy + medical benefits

You will be responsible for the following:

1) Subject Recruitment and follow up

2) Research Documentation / Administrative duties

· Conduct research study activities like patient recruitment, data collection and data management.

· Assist in data collection from electronic health records.

· Set up and maintain study investigator files, including records of consent taken and blood collection.

· Maintain study records in databases such as Redcap and in electronic health record systems.

· Responsible for maintaining strict adherence to research protocols i.e., HBRA.

· Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.

· Prepare necessary documentation for audit purposes.

· Coordinate the submission of new IRB applications, study amendments and annual reports.

· Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements and local regulations.

· Assist with any other duties of a similar nature that are delegated by the PI.

Requirements

· Bachelor Degree in Science/ Public Health/ Social Science

· Able to adapt in a fast-paced environment.

· Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)

Please submit your updated resume in MS Words format by using the APPLY NOW BUTTON.

**We regret to inform that only shortlisted candidates would be notified.

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by company relating to this job application.

Kenneth Isaac Peter

Registration Number: R

MCI Consulting Pte Ltd (EA Licence: 13C6730)

Our team is seeking an individual with the following responsibilities:

Key Responsibilities:

• Screen patients for study eligibility and communicate the study aims to potential participants.
• Obtain consent and administer study questionnaires.
• Follow up with study participants and maintain accurate records.
• Collaborate with research teams, clinicians and clinic staff to ensure research study needs are met.
• Achieve research deliverables within tight timelines.
• Conduct patient recruitment, data collection and management activities.
• Assist in collecting data from electronic health records.
• Maintain investigator files and study records in databases.
• Adhere to research protocols and maintain a high standard of professionalism.
• Liaise with investigators, clinicians and laboratory teams to set up clinical workflows.
• Prepare documentation for audit purposes.
• Coordinate IRB applications and annual reports.

Requirements:

• A minimum degree in a relevant science or medical field.
• Comfortable working at least half days.

Contact Information:

Please send your updated resume to the email address provided.

Clinical Research Associate

The role of Clinical Research Coordinator involves supporting the implementation and management of clinical trials.

• Recruitment, scheduling, and data entry are key responsibilities in this position.
• Patient screening and consent taking are also crucial tasks that require effective communication skills.
• Study questionnaires and participant follow-up activities will be carried out as part of the job duties.

Key Responsibilities:

• Collaborate with research teams, clinicians, and other relevant departments to ensure study requirements are met.
• Ability to work under tight timelines, set realistic targets, and achieve project deliverables is essential.
• Data collection, management, and analysis will be performed as part of the job.

Job Requirements:

• A minimum degree in a relevant science or medical field is required.
• Able to work flexible hours with at least half days per week.

Maintain the highest professional conduct and record-keeping standards in accordance with local regulations and hospital policies.

• Conduct subject recruitment, screening, scheduling, and data entry.
• Communicate study objectives to participants.
• Administer study questionnaires and manage follow-up.
• Collaborate with clinicians and internal departments.
• Perform data collection and maintain documentation.

• Bachelor's degree in Science, Public Health, or Social Science.
• No prior experience required.
• Strong interpersonal and communication skills.

Job Description

We are seeking a highly motivated and detail-oriented Research Coordinator to join our team. As a key member of the research team, you will be responsible for assisting the Principal Investigator with collection of clinical data and data management for Lymphoma and Sarcoma research.

The successful candidate will have excellent organizational and communication skills, with the ability to work independently and as part of a team. They will also have strong problem-solving skills, with the ability to think critically and make sound judgments.

In this role, you will assist with:

• Collection of clinical data and data management
• Implementation and coordination of research projects
• Screening, recruitment, incident event reporting, data entry, biological specimen collection and processing

You will also be responsible for adhering to Good Clinical Practice (GCP) guidelines, protocols, and regulatory compliances.

To be successful in this role, you will need:

• Degree/Diploma in Life Science or its equivalent
• No prior research experience is required, although it will be an added advantage
• Proficient in Microsoft Office applications
• Good interpersonal and communication skills; and comfortable interacting with patients, doctors, nurses, and other healthcare professionals
• Meticulous, a good team player, independent and self-motivated with good time management abilities

This role offers:

• A dynamic and supportive work environment
• Opportunities for professional growth and development
• Competitive salary and benefits package

If you are a motivated and detail-oriented individual with a passion for research, we encourage you to apply for this exciting opportunity.

Clinical Research Coordinator (Govt Hospital)

Location: Queenstown

Working Hours: Mon-Fri, 8.00am-4.30pm

Saturdays, 8.00am - 12.30pm

Duration: 6 Months Renewable contract

Salary: Up to $3400

Benefits:

• Government Hospital - Stable industry
• AWS + 2-3 months performance bonus + yearly salary increment
• Good leave policy + medical benefits

You will be responsible for the following:

1) Subject Recruitment and follow up

2) Research Documentation / Administrative duties

· Conduct research study activities like patient recruitment, data collection and data management.

· Assist in data collection from electronic health records.

· Set up and maintain study investigator files, including records of consent taken and blood collection.

· Maintain study records in databases such as Redcap and in electronic health record systems.

· Responsible for maintaining strict adherence to research protocols i.e., HBRA.

· Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.

· Prepare necessary documentation for audit purposes.

· Coordinate the submission of new IRB applications, study amendments and annual reports.

· Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements and local regulations.

· Assist with any other duties of a similar nature that are delegated by the PI.

Requirements

· Bachelor Degree in Science/ Public Health/ Social Science

· Able to adapt in a fast-paced environment.

· Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)

Please submit your updated resume in MS Words format by using the APPLY NOW BUTTON.

**We regret to inform that only shortlisted candidates would be notified.

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by company relating to this job application.

Kenneth Isaac Peter

Registration Number: R

MCI Consulting Pte Ltd (EA Licence: 13C6730)

Highlights:

• West and Central Area
• Includes AWS, Performance Bonus, & Variable Bonus
• Great Medical Benefits
• Office Hours
• Near MRT

Job Description:

• Managing data and database
• To assist in screening and recruiting eligible patients for research purposes.
• Be involved in writing and reviewing of literature and research papers, to present findings and assist in developing collaborations.
• To assist in project management and providing guidance to juniors.
• To perform administrative and related duties such as data entry and analysis (both qualitative and quantitative), manuscript writing and submission, literature reviews, grants/ethics applications etc.

Job Requirements

• Min. Degree Holder in Sciences/Public Health/Social Sciences.
• Preferably with 1-2 years of experience in healthcare.
• Experienced in research trails and with nursing background will be advantageous.
• Good proficiency with MS Office applications (Excel) and expertise in data analysis (including R, Python, SPSS, STATA) .
• Open to candidates with internship experience

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.*

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JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Avena Esther

EA Personnel Reg No: R

Responsibilities

You will assist the principal investigator to develop and implementation:

· To prepare documents for and facilitate regulatory Approvals

· To facilitate the signing of project agreements with external collaborators.

· To implement and monitor programme activities and workflow.

· To facilitate programme-related outreach events and training sessions.

· Subject's consent taking

· Scheduling study-related appointments for research subjects

· Completing data collection forms

· Conducting surveys or questionnaires

· Managing the study-related equipment

· Handling queries by research subjects

Requirements

· Degree in Nursing, Biological Science, Pharmacy or other healthcare related discipline.

· Able to work independently

· Able to adapt in a fast-paced environment

Interested candidates please send in your resume to:

EA Personnel: Valerie Yong Kian Fung

CEI No.: R

Recruit Express Pte Ltd, EA License No.: 99C4599

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Job Category: Research

Posting Date: 27 Mar 2025

Job Description:

You will provide research support service for clinical research, in accordance to the applicable regulatory, Good Clinical Practice and protocol requirements. You will work closely with the Principal Investigators (PIs), to assist them with organisation of study initiation meetings, IRB submission, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.

You will support and participate in the SGH mission of providing quality patient care, education, and research.

Job Requirements:

1. Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management
2. Fresh graduate or with at least one year of relevant experience
3. Proficient in using MS Office software
4. Effectively bilingual
5. Excellent oral and written communication skills