793 Clinical Research jobs in Singapore

The Division of Allergy & Immunology is seeking a Research Assistant to join their team. The successful candidate will be responsible for conducting various research projects in Paediatric Allergy & Immunology, ensuring the timely completion of study measures and achieving high-quality deliverables.

The RA's primary role will involve performing clinical research-related procedures such as subject screening, recruitment, follow-ups, collection and processing of biological samples, data collection, management, and analysis.

1. Assist with subject screening and recruitment, conduct study visits, perform study procedures, and collect data sets in accordance with approved study protocols;
2. Assist with biological sample processing, storage, and analysis;
3. Maintain and organize investigator site files, prepare and submit documents and/or reports to the ethics committee;
4. Assist with grant status reports and preparation of study progress slides during regular meetings with Co-Is and Collaborators;

The ideal candidate will possess:

1. A Bachelors in Biomedical science, Allied Health or related field;
2. Basic laboratory skills, including pipetting and centrifugation;
3. Ability to work independently and in a team, with an investigative nature, attention to detail, and self-motivation;
4. Outstanding organizational skills and interpersonal communication skills;
5. Basic computer literacy in applications such as MS office, PowerPoint, and Adobe.

Remuneration will be commensurate with the candidate's qualifications and experience. Informal enquiries are welcome and should be made to Alicia Kang at NUS Career Portal.

Formal application: Please submit your application, indicating current/expected salary, supported by a detailed CV (including personal particulars, academic and employment history, complete list of publications/oral presentations, and full contacts of three referees) to the NUS Career Portal.

We are seeking a highly skilled Clinical Research Associate to join our research team. The ideal candidate will be responsible for subject recruitment and follow-up, as well as research documentation and administrative duties.

• Recruit and screen patients for clinical trials, communicating study objectives in layman terms.
• Obtain informed consent from participants and administer study questionnaires.
• Work closely with research teams, clinicians, and clinic staff to ensure research needs are met.
• Manage data collection and entry, including electronic health records.
• Maintain study records and investigator files, adhering to research protocols.
• Liaise with investigators and laboratory teams to set up clinical workflows.
• Prepare documentation for audits and submit new IRB applications and annual reports.

• Bachelor's degree in Science or a related field is required.
• Prior experience in research coordination is an asset.

Clinical Research Coordinator

We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team. The successful candidate will be responsible for conducting research study activities, data collection and management, and ensuring the highest standard of professional conduct.

• Conduct patient recruitment, data collection and data management according to established protocols.
• Assist in data collection from electronic health records and maintain accurate records.
• Set up and maintain investigator files, including consent forms and blood collection records.
• Maintain strict adherence to research protocols and local regulations.
• Liaise with investigators, clinicians and laboratory teams to set up clinical workflows.
• Prepare documentation for audit purposes and coordinate submission of new IRB applications.

• Bachelor's degree in Science, Public Health or Social Science.
• Knowledge of Good Clinical Practice guidelines and the Human Biomedical Research Act.
• Able to adapt in a fast-paced environment and prioritize tasks effectively.

• Opportunity to work in a government hospital setting.
• Chance to develop skills in clinical research coordination.
• Collaborative and dynamic work environment.

• Competitive salary and benefits package.
• Professional development opportunities.
• Supportive team environment.

1. Submit your application, including your resume and cover letter.
2. Attach any relevant certifications or qualifications.
3. Apply now to take the first step towards an exciting career opportunity!

The role of a Clinical Research Coordinator is crucial in the research process, ensuring that studies are conducted efficiently and effectively.

Key responsibilities include:

• Conducting research study activities such as patient recruitment, data collection, and data management.
• Assisting in data collection from electronic health records.
• Setting up and maintaining study investigator files, including records of consent taken and blood collection.
• Maintaining study records in databases and electronic health record systems.
• Ensuring strict adherence to research protocols, including HBRA compliance.
• Liaising with investigators, clinicians, and laboratory teams to set up clinical workflows for research recruitment.
• Preparing necessary documentation for audit purposes.
• Coordinating the submission of new IRB applications, study amendments, and annual reports.

Requirements include:

• A Bachelor's Degree in Science, Public Health, or Social Science.

This position offers a unique opportunity to make a meaningful contribution to the field of clinical research. The successful candidate will have excellent organizational and communication skills, and be able to work independently and collaboratively as part of a team. If you are motivated by the challenge of working in a fast-paced environment and have a passion for research, we encourage you to apply for this exciting opportunity.

The National University Health System (NUHS) offers a prestigious fellowship program in vascular surgery, providing candidates with the opportunity to work alongside a talented team of surgeons and researchers.

As a Clinical Fellow, you will be part of a dynamic department equipped with state-of-the-art facilities and offering a comprehensive range of vascular surgery services. Our team is committed to advancing the field of vascular surgery through research and education.

To qualify for this role, applicants must possess a basic medical degree and be proficient in the English language. This fellowship is recognized by the Singapore Medical Council (SMC), and applicants are subject to registration requirements.

• Key Responsibilities:
• Participate in research projects related to vascular surgery
• Contribute to teaching and educational activities within the department
• Collaborate with healthcare professionals to deliver high-quality patient care

Benefits:

The NUHS offers a supportive work environment, opportunities for professional growth, and access to cutting-edge technology. As a fellow, you will have the chance to enhance your skills and contribute to the development of innovative solutions in vascular surgery.

This is an exceptional opportunity for motivated individuals to take their career to the next level and make a meaningful contribution to the field of vascular surgery.

We are seeking a highly skilled and organized individual to coordinate and conduct clinical research studies in a healthcare setting.

This role involves recruiting and scheduling study participants, screening for eligibility, explaining study objectives, and obtaining informed consent. You will also be responsible for administering study questionnaires, conducting follow-ups, and maintaining accurate records.

The ideal candidate will possess strong interpersonal and communication skills, with the ability to work effectively with patients, clinicians, and multidisciplinary teams. A minimum degree in any related field is required, with prior experience in clinical research or healthcare settings preferred.

• Subject Recruitment & Follow-Up: Recruit and schedule study participants, screen for eligibility, explain study objectives, and obtain informed consent.
• Research Documentation & Administrative Duties: Conduct study procedures, including patient recruitment, data collection, and entry. Maintain study databases, extract data from electronic health records, and ensure compliance with study protocols and regulations.
• Collaborate with Clinicians & Research Teams: Work closely with investigators, clinicians, and lab staff to set up workflows for recruitment across departments.

• Minimum Degree in Any Related Field
• Prior Experience in Clinical Research or Healthcare Setting (Preferred)
• Strong Interpersonal and Communication Skills
• Familiarity with Research Systems and Ethical Guidelines

• Ongoing Training and Professional Development Opportunities
• A Collaborative and Supportive Work Environment
• The Chance to Make a Real Difference in Patient Care

Clinical Research Coordinator Job

The Clinical Research Coordinator will work closely with investigators to conduct clinical trials. This role requires the ability to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials Operations' Standard Operating Procedures.

• Key Responsibilities include:
• Accomplishing the study's target enrolment as per agreed study timelines or shorter through effective recruitment strategies.
• Regular discussion or follow-up with study team on subject screening & recruitment rates e.g. email communication or team meetings with Drs.
• Timely response/followup to email enquiries within 10 working days or less.
• Fostering good working relationships and collaborating effectively across all streams to promote operational efficiency
• Invoicing is carried out on time and payment can be received with minimal delays.

Required Skills and Qualifications:

• Degree in Nursing, Degree in Medicine, Pharmacy or Healthcare / biological sciences, preferably with experience in clinical trials or clinical research.
• 1-2 years experience in the conduct of clinical trials, specializing in Haematology / Oncology interventional trials, governed under Health Product Act.
• Must have knowledge of setting up cell therapy trials.
• Must already been trained in ICH GCP.
• Meticulous and possesses good organizational and time management skills.
• Good communication and interpersonal skills.
• Independent learner, Meticulous and possesses good organizational and time management skills.
• Team player and work well with external collaborators and partners.
• Proactive in learning and helping other CRCs in issues with trial management

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