395 Medical Project jobs in Singapore

Location: Buona Vista
Salary: $30/hr
Working hours: Mon-fri, Office hours

Responsibilities:

• Provides assistance to the research team

• Screens and recruits suitable patients to participate in the research project

• Briefs patients on research background and rationale and to obtain their consent of participation

• Collects data from patients' medical records and research statistics

• Helps document adverse events / reactions that arise

• Performs phlebotomy and venepuncture when required

Requirements:

• Minimum Degree/ Diploma in Nursing

• Min 3 years' experience in Hospital

If interested, please send me your most updated resume to WA: or email me at:

All candidates' information will be treated with the strictest confidence

Katherine Carlen

CEI.No: R

Recruit Express Pte Ltd

EA Licence No: 99C4599

We are currently seeking clinicians to fill a Medical Research Doctor role.
You will work with our Global team of research and clinical professionals to facilitate the translation of research data and quality improvement programs into clinical practice and improvement of patient care. The role includes assisting with drafting and reviewing documentation and publications, project coordination and liaison with project teams, as well as presentation to external stakeholders and conference participation.
This is a fantastic opportunity to become involved in medical management and quality improvement projects with an internationally recognised research organisation.
This role offers home-based working from Singapore or hybrid working from our offices in Cambridge and Norwich, UK, on a full or part-time basis, with flexible working hours that can fit alongside caring arrangements or other clinical/research commitments.
Primary Responsibilities
To contribute to medical quality improvement programs.
To continually assess the benefit of our quality improvement programs to patients, and tailor the programs to maximise their real-life application in a clinical setting.
Review and contribute to scientific documents and publications (including proposals and reports).
To independently develop ethics applications for projects.
To contribute to new and existing projects with respect to considering practical medical issues and clinical application; and to understand EMR data and coding systems and give guidance on the application of data to projects.
Review and complete presentations, abstracts, and posters.
Communication and liaison with internal teams across various global locations.
Liaison with study sponsors and steering committee experts.
Presentations and calls with external stakeholders.
Participation and presentations at international medical/scientific conferences.
Qualifications
Doctor of medicine.
Minimum of 3 years of clinical experience ideally gained within the UK.
Clinical experience or scientific study in the field of respiratory medicine is an advantage.
Experience and Key Skills
UK clinical experience is preferred, ideally within NHS Primary Care.
An interest in research and scientific studies.
Experience in scientific writing, publication of peer-review journal publications is preferred.
Client relations, liaising with external parties internationally, strong leadership and presentation skills.
Excellent written and verbal English communication skills.
Salary
is dependent on experience.
Contact Us
Please send your CV with a covering letter summarising your suitability for the role to All candidates will be required to undertake a remote skills test prior to interview. We look forward to hearing from you.
#J-18808-Ljbffr

Job Description

Oversight of engineering projects for contract manufacturing in medical devices, from conception to completion involves identifying and mitigating potential risks and issues. Closely working with cross-functional teams enables the prompt resolution of manufacturing problems.

Establishing process flow and inspection criteria for all processing steps ensures compliance with quality standards. Improving production requires excellent project management skills to ensure timely completion within budget and quality requirements.

To excel in this role, candidates must possess a Bachelor's degree or diploma in mechanical engineering, electrical electronic & engineering, or a related field. A minimum of 2 years' experience in project coordination/management or a related field is also essential. Strong understanding of medical device regulations and standards is crucial for success.

Candidates should demonstrate strong written and verbal communication skills in English. Technical skills, including knowledge of engineering principles and practices, are also required.

Responsibilities
Provides assistance to the research team
Screens and recruits suitable patients to participate in the research project
Briefs patients on research background and rationale and to obtain their consent of participation
Collects data from patients' medical records and research statistics
Helps document adverse events / reactions that arise
Performs phlebotomy and venepuncture when required
Requirements
Minimum Degree/ Diploma in Nursing
Min 3 years’ experience in Hospital
Only Nurses with SNB license NEED APPLY
Interested candidates please send a copy of your resume in MS Word to

Cameron Tan
Outsourcing Team
Company Reg. No. W
EA Licence No. 99C4599
#J-18808-Ljbffr

Responsibilities:

• Provides assistance to the research team

• Screens and recruits suitable patients to participate in the research project

• Briefs patients on research background and rationale and to obtain their consent of participation

• Collects data from patients' medical records and research statistics

• Helps document adverse events / reactions that arise

• Performs phlebotomy and venepuncture when required

Requirements:

• Minimum Degree/ Diploma in Nursing

• Min 3 years’ experience in Hospital

Only Nurses with SNB license NEED APPLY

Interested candidates please send a copy of your resume in MS Word to

Cameron Tan

Outsourcing Team

Company Reg. No. W

EA Licence No. 99C4599

Location: Buona Vista
Salary: $30/hr
Working hours: Mon-fri, Office hours

Responsibilities:
• Provides assistance to the research team
• Screens and recruits suitable patients to participate in the research project
• Briefs patients on research background and rationale and to obtain their consent of participation
• Collects data from patients' medical records and research statistics
• Helps document adverse events / reactions that arise
• Performs phlebotomy and venepuncture when required

Requirements:
• Minimum Degree/ Diploma in Nursing
• Min 3 years’ experience in Hospital

If interested, please send me your most updated resume to WA: or email me at:

All candidates’ information will be treated with the strictest confidence

Katherine Carlen

CEI.No: R

Recruit Express Pte Ltd

EA Licence No: 99C4599

Job Overview

This is an exciting opportunity to join a research team as a Clinical Research Coordinator. In this role, you will be responsible for providing critical support to the research team in the conduct of clinical trials.

Key Responsibilities:

• Assist the research team in coordinating and implementing clinical trial protocols.

• Screen and recruit suitable patients to participate in clinical trials.

• Brief patients on the research background and rationale and obtain their consent for participation.

• Collect data from patient medical records and research statistics.

• Document adverse events or reactions that arise during the trial.

• Perform phlebotomy and venepuncture when required.

Requirements:

• A minimum degree or diploma in nursing.

• A minimum of 3 years' experience in a hospital setting.

Why This Role?

This is an excellent opportunity for a dedicated and detail-oriented individual to make a real difference in the lives of patients participating in clinical trials.

What We Offer:

• A competitive salary package.

• Ongoing training and development opportunities.

• A dynamic and supportive work environment.

Location: West/ Central
Salary: Up to $3,400/month
Duration: Project basis - 6 months (renewable)
Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM

Job scope:
- Recruit and screen patients based on study eligibility, explaining study goals clearly.
- Obtain consent, administer questionnaires, and follow up with participants.
- Coordinate closely with research teams, clinicians, and clinic staff to meet study needs.
- Manage tight deadlines and achieve research targets.
- Conduct patient recruitment, data collection, and data management.
- Use databases like Redcap and hospital systems to keep accurate records.
- Ensure strict compliance with research protocols and regulations.
- Work with investigators and labs to set up clinical workflows for recruitment.
- Prepare documents for audits and assist with IRB submissions and reports.
- Maintain professional standards and adhere to hospital policies and ethics.
- Perform other related duties as assigned by the Principal Investigator (PI).

Job Requirements:
- Min. Degree in Science/ Public Health/ Social Science or any relevant field
- Adaptable, strong communication and interpersonal skills
- No experience as training will be provided

For interested applicants, please send your updated resume to:
All candidates' information will be treated with the strictest confidence
Melissa Zhang Zhiqi (Mezzo)
R
Recruit Express Pte Ltd
99C4599

Clinical Research Coordinator Role Summary:

• This role involves coordinating research activities to support the success of clinical studies.

About the Job:

The selected candidate will be responsible for recruiting and screening patients, obtaining consent, administering questionnaires, and following up with participants. They will also coordinate closely with research teams, clinicians, and clinic staff to meet study needs.

Key Responsibilities:

• Recruit and screen patients based on study eligibility, explaining study goals clearly.
• Obtain consent, administer questionnaires, and follow up with participants.
• Coordinate closely with research teams, clinicians, and clinic staff to meet study needs.
• Manage tight deadlines and achieve research targets.
• Conduct patient recruitment, data collection, and data management.
• Use databases like Redcap and hospital systems to keep accurate records.
• Ensure strict compliance with research protocols and regulations.
• Work with investigators and labs to set up clinical workflows for recruitment.
• Prepare documents for audits and assist with IRB submissions and reports.

Requirements:

• Min. Degree in Science/ Public Health/ Social Science or any relevant field.
• Adaptable, strong communication and interpersonal skills.
• No experience as training will be provided.

About You:

This is a project-based role that requires flexibility and adaptability. The selected candidate will work closely with the research team to ensure the successful execution of studies.