180 Clinical Trials jobs in Singapore

Job Opportunity: Clinical Trial Assistant

• Schedule appointments and manage study-related tasks for research subjects.
• Conduct surveys and gather data through questionnaires.
• Manage equipment and supplies necessary for the study.
• Handle queries from research participants in a professional manner.

• Able to work independently with minimal supervision.
• Adapt quickly to changing environments and priorities.

Interested applicants may send their resume in MS Word format to Cameron in the Outsourcing Team at Recruit Express Pte Ltd, EA License No. 99C4599.

Clinical Research Coordinator Role Overview:

The successful candidate will provide administrative support for clinical trials and research projects in accordance with international standards and protocols.

Key Responsibilities include:

• Coordinating clinical trial activities including data management, monitoring, and study close-out
• Communicating effectively with Principal Investigators (PIs), sponsors, and other stakeholders
• Preparing and submitting regulatory documents such as CIRB & HSA applications
• Assisting with subject recruitment and retention strategies
• Maintaining accurate records of study equipment and investigational products
• Contributing to quality control and assurance processes
• Providing administrative support to the PI and sponsor companies

Requirements:

• Degree in Life Sciences or related field
• Fluent written and spoken English language skills
• Intermediate computer skills (MS Office)
• Strong team player with excellent communication skills

Key Skills: Quality Control, Clinical Research, Quality Assurance, Healthcare, Administration, Data Entry, MS Office, Clinical Trials

Clinical Research Nurse

The successful candidate will be responsible for screening study participants according to regulatory guidelines and ethical standards.

• Conduct informed consent discussions and ensure participants understand the study's requirements.
• Monitor patient progress and collect data during clinical trials, ensuring accurate documentation.
• Administer study-related interventions as per protocol, including medications and treatments.
• Conduct assessments and follow-ups with participants, addressing any concerns and providing education.

Key Responsibilities Include:

• Screening and enrollment of patients in accordance with protocol.
• Collection of data from patients during their participation in studies.
• Monitoring of patients' responses to treatment and collection of relevant data.
• Assessment of patient safety and reporting of any adverse events or reactions.

• Diploma/Degree in Nursing
• Valid SNB & BCLS required
• Able to perform IV Cannulation and Phlebotomy

This role offers a unique opportunity to work on cutting-edge research projects while developing your clinical skills and knowledge.

Study Coordinator Role

This position is responsible for coordinating various aspects of a clinical trial, including scheduling appointments and managing data collection forms. In addition to these key responsibilities, the role also involves conducting surveys or questionnaires and overseeing study-related equipment.

About this Job

• The ideal candidate will have excellent organizational and communication skills.
• They must be able to work effectively in a fast-paced environment.

Key Responsibilities

Scheduling appointments for research subjects and completing data collection forms are fundamental tasks in this role. Furthermore, conducting surveys or questionnaires and managing study-related equipment are essential duties.

Qualifications and Skills

• Independence and self-motivation are crucial qualities for this position.
• Able to adapt quickly in a dynamic environment.

What We Offer

This role provides an opportunity to work on a critical aspect of a clinical trial, contributing to the advancement of medical research. The successful candidate will have the chance to develop their skills and gain valuable experience in a dynamic field.

The Senior Manager/ Manager assumes responsibility to support Director for all administrative and operational functions of the Clinical Trials and Research Centre (CTRC). He/She is responsible for assisting in supervising and developing the staff at CTRC in providing quality clinical research related services to the hospital, investigators, and sponsors/ clinical research organisations (CRO).

The job responsibilities include:

• Ensure that all trials managed by CTRC are conducted in strict adherence to regulatory, ethical, Good Clinical Practice and protocols.
• Oversee the effective allocation and management of resources to support the execution of trials within CTRC.
• Design and implement a comprehensive training program for CTRC staff to maintain compliance with latest regulations and guidelines and conduct periodic review on staff performance.
• Oversee talent retention and succession planning.
• Building a strong pipeline to meet CTRC manpower needs.
• Provide operational oversight for CTRC's day-to-day activities and ensuring a seamless and effective workflow.
• Oversee and manage the CTRC's budget and ensure accurate financial planning, timely billing, and effective accounts management processes.
• Monitor expenditures to maintain alignment with departmental financial goals.
• Lead quality assurance and quality control initiatives to enhance CTRC's compliance, service quality and competitiveness.
• Develop and monitor CTRC's key performance indicators (KPIs), i.e. study start-up timelines, budget, staff performance etc. for continuous improvement.
• Collaborate with the Director to develop and implement business strategies aimed at expanding the CTRC's reach and impact.
• Build and strengthen partnerships to enhance clinical trials/ clinical research opportunities and drive growth initiatives that align with the CTRC's goals.
• Participate in departmental activities, contribute to institutional initiatives, and fulfil additional duties as required by management

Job Requirements:

• Possess a good general degree, preferably in healthcare related fields.
• Minimum of 8-10 years relevant clinical trial/research work experiences, with at least 4 years in a supervisory/management capacity.
• Possess a strong track record of performance and leadership/ people developer.
• Possess excellent interpersonal, communication, coordination and time management skills.
• Extensive experience in clinical trials operations and management
• Able to work independently and meticulously.
• Effective presentation and organisational skills

Job description

• To closely involved in patient/volunteer recruitment, coordination and follow‐up for clinical studies.
• To liaise and communicate with all team members of the research projects to ensure smooth running of the project.
• To provide administrative and secretarial support to research projects, such as organizing regular meetings to maintain regular communication with other members of the research team and procurement of materials.
• To assist clinical study database formation, data collection.

Interested candidates please send in your resume to:



Cameron

Outsourcing Team

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

Job Description

• Scheduling study-related appointments for research subjectsCompleting data collection forms
• Conducting surveys or questionnaires
• Managing the study-related equipment
• Handling queries by research subjects

Requirements
Able to work independently
Able to adapt in a fast-paced environment

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

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

Job Description

• Scheduling study-related appointments for research subjectsCompleting data collection forms
• Conducting surveys or questionnaires
• Managing the study-related equipment
• Handling queries by research subjects

Requirements
Able to work independently
Able to adapt in a fast-paced environment

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

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

Job Description

• 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

• Able to work independently
• Able to adapt in a fast-paced environment

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



Cameron

Outsourcing Team

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