What Clinical Research Associates Jobs are in Singapore?

Job Description

• Ensures proper investigational product (IP) management which includes sourcing, receipt, storage, preparation, dispensing, labelling, inventory accountability, reconciliation, retention, destruction and documentation according to the study protocol

• Assists Clinical Research Technologists in maintaining proper functioning of all pharmacy equipment.

• Reviews and provides feedback during protocol development where applicable

• Reviews and updates Pharmacy local standard operation procedures as appropriate

• Provides coaching to Locum Pharmacists and Pharmacy Technicians/Assistants as needed on IP management and aseptic compounding

Requirements

• Singapore Registered Pharmacist

• Previous Hospital Pharmacy Experience

• Experience in working in cleanroom or manufacturing setting

• General GMP and GDP knowledge

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

PURPOSE OF THE ROLE

In this role, you will drive both business development andoperational excellence for our Clinical Trial Projects. Your keyresponsibilities will include:

•   Managing Requests for Information (RFIs) andRequests for Proposals (RFPs)

•   Maintaining and refining costing models

•   Overseeing contracting activities

•   Supporting capacity and resource planning

•   Conducting data analysis to enhance projectperformance

REQUIREDQUALIFICATIONS AND EXPERIENCE

•   A diploma or degree in a science orhealth-related field

•   Prior experience in early-phase clinicalresearch is preferred

Interested candidates please send in your resume to:

Anthea Lim

Outsourcing Team

Company Reg. No. W

EA Licence No. 99C4599

The upcoming Eastern General Hospital (EGH) aims to provide excellent healthcare and promote healing centered around each person. When operational, EGH will provide a comprehensive range of inpatient and outpatient clinical specialties and healthcare services, covering emergency, acute and secondary care. EGH’s vision is to be a hospital for the community and a great workplace for staff. It seeks to do so by harnessing innovative technologies in patient care, journeying closely with patients and the community to lead healthier and more fulfilling lives, and being an employer of choice that empowers staff in their careers.

In this role, you will support the department and Medical Board through comprehensive data analytics and policy implementation. Your responsibilities include developing standardised analytical frameworks, performing data extraction, cleaning, analysis and reporting of clinical and non-clinical datasets, conducting manpower projections, as well as undertaking population health analytics involving quantitative, qualitative and geospatial data.

You will also support the planning, development and implementation of licensing, quality, safety, and clinical policy initiatives. You will coordinate licensing related matters and preparation of the hospital for audits; support the Quality Audit Committees and Clinical Committees with meetings, follow-up actions and incident monitoring; and contributing to the development, implementation and monitoring of institutional-level clinical policies. Additionally, you will organise stakeholder engagement sessions and performing other duties as assigned to ensure effective operational support across quality, safety and regulatory functions.

Requirements

• Bachelor’s Degree in any discipline with at least 4 years of relevant working experience or Diploma in any discipline with at least 10 years’ relevant working experience
• Experience in healthcare sector (hospital or community setting) is an advantage
• Prior experience with basic data analytics and is keen to concurrently work on clinical policies and governance OR experience with clinical governance, and is keen to concurrently work on data analytics projects would be ideal
• Knowledge of relevant International Statistical Classification of Diseases & Related Health Problems and Classification of Health Interventions/Surgeries would be an advantage
• Proficient with Microsoft Office applications (Word, Excel, PowerPoint)
• Team player with the ability to manage cross-functional and institutional relationships
• Possess strong communication and interpersonal skills and the ability to engage various stakeholders in a fluid environment and a growing organisation
• Good analytical, presentation and writing skills as well as ability to work under tight deadlines
• Ability to handle complex, ambiguous and challenging situations under fast-paced and evolving conditions

Asian Thoracic Oncology Research Group (ATORG) is the coordinating platform for translational research in Asia. Its mission is to advance medical knowledge of lung cancer and improve health outcomes of patients through clinical studies and scientific events. ATORG operates under National Cancer Centre Singapore.

We are looking for a Research Fellow who will provide critical support in the design, writing, and operational documentation of multi-country investigator-initiated trials (IITs) and translational oncology studies under the ATORG platform. This includes drafting study protocols, scientific reports, stakeholder materials, and contributing to consensus meetings and academic outputs.

This role is ideal for a motivated and detail-oriented individual with strong scientific writing skills and an interest in driving precision oncology research across Asia.

Main Responsibilities:

1. Study Design and Protocol Development (40%)

• Draft and refine clinical and translational protocols, including Synopsis, Study flow diagrams, Schedules of assessments (SoA), and biomarker sections
• Coordinate protocol input from PIs, Statisticians, Clinicians, and vendors
• Adapt study designs to site capabilities, operational constraints, and scientific objectives

2. Scientific & Grant Writing (30%)

• Develop Abstracts, poster presentations, and manuscripts for submission to Scientific conferences and journals
• Prepare Grant applications, Letters of Intent (LOIs), and scientific reports for academic and industry sponsors
• Draft meeting materials for advisory boards, working groups, and regulatory discussions

3. Stakeholder Engagement & Meeting Support (20%)

• Support scientific communications with local and regional collaborators, including meeting minutes, presentation decks, and briefing materials
• Liaise with site investigators, pharma sponsors, CROs, and academic partners to support scientific alignment across projects
• Contribute to preparation and documentation of region

4. Strategic Input & Innovation (10%)

• Provide input into vendor evaluations, consensus statement writing, and research planning documents
• Assist with the development of SOPs, training materials, and collaborative frameworks to improve ATORG’s scientific processes

Key Requirements:

• Master’s degree in biomedical sciences, cancer biology, molecular medicine, public health, or related field
• At least 2–3 years of relevant research or clinical trial experience, particularly in scientific documentation or study design
• PhD in a related field OR equivalent track record of scientific output (e.g., peer-reviewed publications, lead authorship on abstracts)
• Familiarity with clinical trial protocol writing, GCP principles, or ethics submissions
• Prior experience in oncology research, translational studies, or regional research collaborations

Advantageous Skills to Have:

• Scientific Writing & Communication: Excellent ability to translate complex scientific and clinical data into clear, accurate protocols, manuscripts, and presentations.
• Analytical & Problem-Solving: Strong capability to evaluate scientific feasibility, identify risks, and propose practical solutions.
• Stakeholder Engagement: Skilled in managing relationships with investigators, sponsors, vendors, and internal teams across different cultures and geographies.
• Organisational & Project Management: Ability to manage multiple projects concurrently, meet deadlines, and maintain attention to detail.
• Regulatory & Compliance Awareness: Competence in ensuring study design, documentation, and publications comply with international and local regulations, SOPs, and ethical standards.
• Technical proficiency with MS Office, reference management software, and clinical trial management systems (CTMS) is desirable.

Job Description

•   Ensures proper investigational product (IP)management which includes sourcing, receipt, storage, preparation, dispensing,labelling, inventory accountability, reconciliation, retention, destruction anddocumentation according to the study protocol

•   Assists Clinical Research Technologists inmaintaining proper functioning of all pharmacy equipment.

•   Reviews and provides feedback during protocoldevelopment where applicable

•   Reviews and updates Pharmacy local standardoperation procedures as appropriate

•   Provides coaching to Locum Pharmacists andPharmacy Technicians/Assistants as needed on IP management and asepticcompounding

Requirements

•   Singapore Registered Pharmacist

•   Previous Hospital Pharmacy Experience

•   Experience in working in cleanroom ormanufacturing setting

•   General GMP and GDP knowledge

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

Join a dynamic clinical research team where you will play a key role in supporting clinical studies that contribute to advancing healthcare. If you have a keen eye for detail, enjoy working in a fast-paced environment, and are passionate about research excellence, this opportunity could be the perfect fit.

Key Responsibilities

• Coordinate and support patient recruitment, screening, enrolment, and follow-up activities in accordance with study protocols.
• Work closely with investigators and the research team to achieve study enrolment targets.
• Explain study procedures and eligibility criteria to participants while ensuring informed consent is obtained and documented appropriately.
• Maintain compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Review source documents and ensure timely, accurate, and complete data entry into case report forms and electronic data capture systems.
• Prepare and maintain essential study documentation, regulatory files, and research records for audits and inspections.
• Monitor study progress, track protocol deviations, adverse events, and follow up on required reporting.
• Coordinate study materials, investigational products, and research supplies where applicable.
• Liaise with investigators, study sponsors, and internal stakeholders to ensure smooth study operations.
• Attend study meetings, investigator meetings, and research discussions as required.
• Uphold patient confidentiality and maintain the highest standards of ethical clinical research practices.

Requirements

• Degree in Science, Life Sciences, Public Health, Health Sciences, Pharmacy, Medicine, Nursing, or a related discipline.
• Prior experience in clinical research, study coordination, research administration, or related healthcare research environments is advantageous.
• Familiarity with Good Clinical Practice (GCP), clinical research regulations, and ethical guidelines is an advantage.
• Meticulous with strong organisational and analytical skills.
• Able to work independently while collaborating effectively within a multidisciplinary team.
• Strong communication and interpersonal skills with the ability to manage multiple priorities.

Interested applicants are invited to submit their updated resume to with the subject header "Clinical Research Coordinator" .

Leon Leong De Cong
R
Recruit Express Pte Ltd
EA License No. 99C4599

Responsibilities

·   Provide and coordinate nursing care to patientswho participate in research studies

·   Enforce standards of care and professional codesof conduct.

·   Ensure safety and well-being of study subjects,and all clinical trial data are reliable

·   Recognise emergency situations and assist intreatment procedures

·   Prepare research metrics and reports forsubmission

·   Perform intensive monitoring of researchsubjects in early phase clinical trials

Job requirements

·   Diploma / Bachelor’s Degree in Nursing

·   Registered nursing qualification and registered withSingapore Nursing Board (SNB) with valid BCLS certificate

·   At least 5 years' clinical nursing experience inClinical Trial

Interested candidates please send in your resume to:

Anthea Yeo

Outsourcing Team

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

Key Responsibilities

• Manage daily inventory activities, including cycle counts, stock reconciliation and inventory adjustments.
• Monitor inventory accuracy and investigate discrepancies to ensure data integrity.
• Manage inventory scrap and prepare reports for expired, damaged or obsolete inventory.
• Support inventory audits and ensure compliance with internal policies and regulatory requirements.
• Analyse inventory and operational data to monitor inventory health, stock levels and key performance indicators (KPIs).
• Prepare reports and dashboards to provide insights on inventory performance and operational trends.
• Identify process gaps and recommend improvements to enhance inventory accuracy and operational efficiency.
• Develop, maintain and improve inventory management SOPs and operational processes.
• Support SAP system enhancements, testing and implementation of new features when required.
• Participate in inventory-related projects and continuous improvement initiatives.
• Work closely with Warehouse Operations, Planning, Customer Service, Quality, Finance and IT teams to ensure efficient inventory management.
• Provide inventory reports and documentation to support internal audits, compliance reviews and management reporting.

Requirements

• Bachelor's Degree in Supply Chain Management, Engineering (Industrial, Mechanical, Materials) or a related discipline.
• Minimum 2 years of experience in inventory control, warehouse operations, logistics or supply chain within the Life Sciences, Medical Device, Clinical Diagnostics or Pharmaceutical industry.
• Experience with SAP EWM, SAP ECC or other Warehouse Management Systems (WMS).
• Proficient in Microsoft Excel and Microsoft Office applications.
• Experience with data analysis, reporting and dashboard tools (e.g. Power BI, Tableau) will be an advantage.
  

All qualified applicants, please send in your resume to:

Tricia Celestine Goh (R )

Recruit Express Pte Ltd | Company Reg. No. W | EA License Number: 99C4599

PURPOSE OF THE ROLE

In this role, you will drive both business development and operational excellence for our Clinical Trial Projects. Your key responsibilities will include:

•⁠ ⁠Managing Requests for Information (RFIs) and Requests for Proposals (RFPs)

•⁠ ⁠Maintaining and refining costing models

•⁠ ⁠Overseeing contracting activities

•⁠ ⁠Supporting capacity and resource planning

•⁠ ⁠Conducting data analysis to enhance project performance

REQUIRED QUALIFICATIONS AND EXPERIENCE

•⁠ ⁠A diploma or degree in a science or health-related field

•⁠ ⁠Prior experience in early-phase clinical research is preferred

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