Research Project Coordinator

1 week ago

Singapore beBeeResearch Full time $52,000 - $67,000

Job Title: Research Project Associate

About the Role

We are seeking a highly organized and detail-oriented Research Project Associate to assist principal investigators in the development and implementation of clinical research and clinical trial protocols.

Key Responsibilities
  • Prepare documents for regulatory approvals by ensuring all necessary information is accurate and complete.
  • Design and develop informed consent forms and data collection forms that meet ICH-GCP and HBRA requirements.
  • Purchase and maintain research supplies, including equipment and materials needed for studies.
  • Execute approved clinical research and clinical trial protocols as directed by principal investigators.
  • Handle queries from research subjects in a timely and professional manner.
  • Take consent from research subjects, ensuring they fully understand the study and its risks.
  • Schedule clinic appointments for research subjects, coordinating with staff and investigators as needed.
  • Complete data collection forms accurately and efficiently, ensuring high-quality data is collected.
  • Set up and enter research data into study databases, maintaining accurate records throughout the study.
  • Administer surveys or questionnaires as required by the study protocol.
  • Manage investigational drugs/devices, following established procedures to ensure safety and efficacy.
  • Set up and maintain investigator study files, organizing and tracking all relevant documentation.
  • Coordinate meetings between investigators and study team members, facilitating communication and collaboration.
  • Ensure timely preparation and submission of study progress reports, meeting regulatory requirements.
  • Prepare for study audits by regulatory authorities, assembling necessary documentation and ensuring compliance.
Requirements
  • Bachelor's degree in a related field, such as life sciences or public health.
  • At least 2 years of experience in research coordination or a related field.
  • Strong organizational and communication skills, with ability to work independently and as part of a team.
  • Attention to detail and accuracy in preparing documents and collecting data.
  • Familiarity with ICH-GCP and HBRA regulations, as well as other applicable laws and guidelines.
  • Ability to learn and adapt to new systems and technologies.
Benefits

This role offers a competitive salary and benefits package, including medical, dental, and vision coverage, as well as opportunities for professional growth and development.

The ideal candidate will be highly motivated and dedicated to delivering high-quality results in a fast-paced environment.

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