Clinical Research Coordinator (1 yr contract) - up to $4k/GOVT/ENTRY LEVEL #HAO

Recruit Express Pte Ltd.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A healthcare staffing agency in Singapore is seeking a Clinical Research Coordinator for a 1-year contract. Responsibilities include overseeing study operations, ensuring regulatory compliance, managing data collection, and recruiting participants. Candidates should hold a degree in Life Sciences. Interested individuals can submit their resume to the provided email.

Qualifications

• Degree in Life Sciences or a related field.
• Ability to oversee clinical trial operations.
• Familiarity with data management in clinical research.

Responsibilities

• Oversee daily trial operations and ensure compliance.
• Act as the primary contact for participants.
• Recruit and screen participants based on criteria.

Skills

Study management

Regulatory compliance

Data collection

Participant recruitment

Team coordination

Safety monitoring

Education

Min Degree in Life Sciences or similar

Job description

Clinical Research Coordinator (1 yr contract) - up to $4k/GOVT/ENTRY LEVEL #HAO

Salary: up to $4000
Duration: 1 year direct contract

Working Days & Hours: Mon-Fri Office Hours

Location: Novena

Job Description:
Study Management:

o Oversee the daily operations of the trial and ensure that the study procedures are conducted in accordance with the approved study protocol.

o Act as the primary contact for participants, including but not limited to scheduling and coordinating study visits, addressing concerns, assisting with app navigation.

o Maintain timely documentation of informed consent, data collection forms (e.g. PHQ-4, PHQ-9, GAD-7, WHODAS 2.0), participant information, study progress, communications, and regulatory affairs.

o Appropriate data management in compliance with necessary regulatory requirements.

Regulatory Compliance:

o Ensure compliance of the trial in adherence to Singapore Guideline for Good Clinical Practice (SGGCP), data protection, and ethical requirements.

Data Collection:

o Administer data collection forms, such as PHQ-4, PHQ-9, GAD-7, WHODAS 2.0, and trial demographics, etc.

Participant Recruitment:

o Conduct screening of potential participants to assess their eligibility based on the inclusion-exclusion criteria.

o Provide study information and obtained informed consent.

o Register participant for enrolment into the research programme.

o Introduce the research programme and app navigation.

Team Coordination:

o Act as the liaison between the relevant organisations for study-related matters.

Safety Monitoring:

o Assist in tracking and reporting adverse events, non-compliance, and protocol deviation.

Job Requirements: Min Degree in Life Sciences or similar

Interested candidates, please submit your resume to: [e-mail]

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)