23 Clinical Testing jobs in Singapore

Responsibilities:

• Identify and develop new business opportunities within the medical solutions industry in the West region.
• Build and maintain strong relationships with existing clients to ensure customer satisfaction and repeat business.
• Deliver technical presentations and demonstrations to potential clients to showcase the features and benefits of the company's medical solutions.
• Understand customer requirements and provide tailored solutions to meet their needs.
• Prepare sales proposals and negotiate contracts with clients.
• Collaborate with internal teams to ensure timely and accurate delivery of products and services to clients.
• Stay up-to-date with industry trends and competitors' offerings to effectively position the company's products and services in the market.
• Attend industry trade shows and exhibitions to network and generate leads.
• Meet or exceed sales targets and contribute to the growth of the company's revenue.
• Provide excellent customer service and support throughout the sales process.

Minimum Requirements:

• Bachelor's degree in Engineering or a related field.
• Prior experience in business development or sales roles within the medical solutions industry.
• Strong understanding of medical solutions and the healthcare industry.
• Excellent communication, negotiation, and presentation skills.
• Proven track record of meeting or exceeding sales targets.
• Ability to build and maintain strong relationships with clients.
• Self-motivated and driven to achieve business growth.
• Willingness to travel within the West region for client meetings and industry events.

Interested candidates who wish to apply for the advertised position, please click 'APPLY' to send in your resume.

This is an exciting opportunity for a Freelance Clinical Trial Nurse to join our research team. As a key member of our team, you will play a vital role in ensuring the success of clinical trials.

• Assist the research team in various tasks related to clinical trials.
• Ensure the smooth execution of trial procedures and protocols.
• Maintain accurate and detailed records of trial progress.

Required Skills and Qualifications:

We are looking for individuals with the following skills and qualifications:

• Strong knowledge of clinical trial procedures and protocols.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.

Benefits:

As a Freelance Clinical Trial Nurse, you will have the opportunity to work on a variety of projects and develop your skills and expertise. You will also have access to ongoing training and professional development opportunities.

Other Opportunities:

Working as a Freelance Clinical Trial Nurse offers many opportunities for career advancement and personal growth. You will have the chance to work with a dynamic team and contribute to the success of clinical trials.

This is a full-time contract position with 5.5 days of office hours per week.

We are looking for a highly motivated and organized individual with a passion for clinical research to join our team as a Research Coordinator.

The selected candidate will be responsible for coordinating studies, managing budgets, and working closely with the Principal Investigator (PI) to achieve project goals.

The ideal candidate will have strong interpersonal skills, experience in clinical research, and knowledge of healthcare administration.

We offer a dynamic and supportive work environment with opportunities for professional growth and development.

The successful candidate will have opportunities for career growth and personal development.

• Coordinate with the team and clinics to set up study sites, including making logistics arrangements and preparing for studies and meetings.
• Manage study budget, tracking expenses, and making financial payments.
• Coordinate studies across multiple sites and collaborate with other teams as needed.
• Monitor study progress and coordinate regular reviews with the study team.
• Assist in preparing study-related presentations and materials.
• Evaluate research results and provide feedback.

• Possess a relevant Diploma or Degree.

• This role is ideal for individuals with a strong understanding of research protocols.
• We are looking for a motivated individual who is passionate about clinical trials.

Job Summary

   We are seeking a skilled Clinical Research Pharmacist to join our team. In this role, you will be responsible for ensuring the proper management of Investigational Product Controlled Drug Therapeutic Product.

   Key Responsibilities:

• Source, receive, store, prepare, dispense, label, and inventory manage Investigational Products.

• Perform extemporaneous preparation, aseptic compounding, and other dispensing activities as required.

• Manage pharmacy operational activities, including inventory control, maintaining cleanliness of pharmacy areas, and environmental monitoring.

• Ensure compliance with regulations regarding randomization and unblinding procedures for clinical trials.

• Maintain equipment in the pharmacy and perform cross-functional duties as needed.

Qualification Requirements

• Registered Pharmacist license in Singapore.

• Experience in compounding or working in a cleanroom or manufacturing setting is preferred.

Job Overview

The Senior Research Nurse Executive plays a pivotal role in ensuring the safety and well-being of study subjects while maintaining the integrity of clinical trial data. This position involves close monitoring of research participants in early phase clinical trials, with a focus on preparing accurate research metrics and reports.

Responsibilities:

• Deliver high-quality nursing care to patients participating in research studies
• Implement and enforce standards of care and professional codes of conduct
• Guarantee the safety and well-being of study subjects and the reliability of clinical trial data
• Identify and respond to emergency situations, providing assistance as needed
• Prepare comprehensive research metrics and reports for submission
• Conduct intensive monitoring of research participants in early phase clinical trials

Requirements:

• Bachelor's Degree in Nursing or relevant field
• Registered nursing qualification and registration with the relevant nursing board, accompanied by a valid BCLS certificate
• Minimum 5 years' experience in clinical nursing, preferably in clinical trials

This is an exciting opportunity to contribute to groundbreaking research in nursing. If you are a motivated and experienced nurse looking for a new challenge, we encourage you to apply.

Key Performance Indicators (KPIs):

• Ensure accurate and timely preparation of research metrics and reports
• Maintain high standards of patient care and safety
• Collaborate effectively with cross-functional teams to achieve research objectives

Benefits:

• Opportunity to work in a dynamic environment and contribute to cutting-edge research
• Chance to develop skills and expertise in clinical trial management
• Competitive compensation and benefits package

Why Join Us:

We offer a supportive and collaborative work environment that fosters growth and development. Our team is dedicated to advancing research in nursing and improving patient outcomes.

We are representing a confidential, fast-growing company at the forefront of dental AI innovation. The company is developing a revolutionary AI-powered screening device/software aimed at transforming early detection and diagnosis in oral healthcare.

To support product validation and global market entry, we are seeking a Clinical Trials Project Manager to lead and manage clinical studies from initiation to close-out.

• Lead and manage end-to-end clinical trial activities (planning, execution, monitoring, and reporting) in alignment with GCP, regulatory requirements, and project timelines
• Collaborate with cross-functional teams including R&D, regulatory affairs, QA, and data science to ensure study objectives are met
• Oversee the selection, initiation, and coordination of clinical trial sites, investigators, and vendors
• Prepare and maintain all clinical trial documentation (protocols, informed consent forms, CRFs, study reports)
• Monitor trial progress, manage budgets and timelines, and mitigate risks proactively
• Ensure compliance with all applicable ethical and regulatory standards including IRB/IEC submissions
• Coordinate data collection and validation in conjunction with the AI/tech team for real-world performance benchmarking
• Report trial milestones and results to internal leadership and external regulatory bodies

• Bachelor's degree or higher in Life Sciences, Biomedical Engineering, Dentistry, Public Health, or a related field
• 3–5 years' experience managing clinical trials, preferably in medical/dental devices or digital health/AI
• Strong understanding of GCP and relevant regulatory frameworks
• Experience with investigator-initiated trials, device/software validations, or real-world data studies is a plus
• Excellent project management and stakeholder coordination skills
• Strong written and verbal communication, especially in technical and regulatory documentation
• Familiarity with dental or radiology clinical environments is advantageous
• Ability to manage multiple priorities in a fast-paced, startup-like environment

Job Overview:

• We are seeking a highly motivated Clinical Project Associate to join our team.
• This role will be responsible for planning and executing study management activities, including timeline development, risk assessment, budget control, and communication with internal and external partners.
• As the focal point of study-level communication, you will ensure seamless collaboration between functional personnel and keep all stakeholders informed of timelines, unanticipated issues, and solutions.

Key Responsibilities:

• Develop and negotiate detailed clinical study budgets in partnership with cross-functional personnel.
• Lead study development in collaboration with internal and external partners.
• Determine and communicate Clinical Trial submission and approval requirements.

Requirements:

• Bachelor's degree in a Science-related field.
• Preferred experience in clinical trial administration.

We are representing a confidential, fast-growing company at the forefront of dental AI innovation . The company is developing a revolutionary AI-powered screening device/software aimed at transforming early detection and diagnosis in oral healthcare.

To support product validation and global market entry, we are seeking a Clinical Trials Project Manager to lead and manage clinical studies from initiation to close-out.

• Lead and manage end-to-end clinical trial activities (planning, execution, monitoring, and reporting) in alignment with GCP, regulatory requirements, and project timelines
• Collaborate with cross-functional teams including R&D, regulatory affairs, QA, and data science to ensure study objectives are met
• Oversee the selection, initiation, and coordination of clinical trial sites, investigators, and vendors
• Prepare and maintain all clinical trial documentation (protocols, informed consent forms, CRFs, study reports)
• Monitor trial progress, manage budgets and timelines, and mitigate risks proactively
• Ensure compliance with all applicable ethical and regulatory standards including IRB/IEC submissions
• Coordinate data collection and validation in conjunction with the AI/tech team for real-world performance benchmarking
• Report trial milestones and results to internal leadership and external regulatory bodies

• Bachelor’s degree or higher in Life Sciences, Biomedical Engineering, Dentistry, Public Health, or a related field
• 3–5 years’ experience managing clinical trials, preferably in medical/dental devices or digital health/AI
• Strong understanding of GCP and relevant regulatory frameworks
• Experience with investigator-initiated trials, device/software validations, or real-world data studies is a plus
• Excellent project management and stakeholder coordination skills
• Strong written and verbal communication, especially in technical and regulatory documentation
• Familiarity with dental or radiology clinical environments is advantageous
• Ability to manage multiple priorities in a fast-paced, startup-like environment

National Cancer Centre of Singapore Pte Ltd

Job Category: Research

Posting Date: 20 Mar 2025

We are looking for an Assistant Manager OR Manager with sufficient professional experience and skills to fulfill a specialist role that can contribute to the development of the clinical trial program within National Cancer Centre Singapore (NCCS). The role will mainly assist our Clinical Trials Office to review and finalize contracts related to clinical trials for the Division of Clinical Trials & Epidemiological Sciences (CTE).

Main Duties:

1. Assist to review clinical trial contracts and work closely with the SingHealth Legal Department to negotiate agreement terms with commercial sponsors, CROs, academic institutions or international trial groups.
2. Assist in checking hard copy contract documents and obtaining signatures from the NCCS’s signatories.
3. Keep track of agreement timelines and chase for replies if a party has not replied for the past two weeks.
4. Supervise and provide advice to the executives of the Feasibility Team in NDA negotiation and to act as back-up for such review and negotiation during manpower shortage.
5. Assist in approving online payments in APIMS, training applications in PeopleConnexion (SuccessFactors) and any other online applications assigned.
6. Help to oversee financial and insurance reporting to CTCC as well as annual NMRC reporting.
7. Assist in submission and updating of the clinicaltrials.gov, check and approve archiving costs and payment to archiving company and MRO.
8. File and maintain executed contracts and ensure these are stored securely to maintain confidentiality and prevent loss or damage.
9. Perform any other duties assigned by the supervisors or the Clinical Trials Office higher management staff.

Main Requirements:

1. A recognised degree, with at least 6 to 8 years of relevant experience in negotiating clinical trial contracts or research study contracts as well as experience in staff supervision.
2. Preference for individuals with good knowledge of clinical trial conduct procedures.
3. Well versed in relevant laws and regulations applicable to trial conduct including HBRA, Health Products and Medicines Act, Health Product (Clinical Trial) Regulation, PDPA and ICH GCP.
4. Strong communication and writing skills, good command of language, good people skills and strong ability to be a good team player.
5. Strong leadership and management skills.