Haematology Clinical Trial Coordinator - Part-Time

Barwon Health

Geelong

Presencial

AUD 64.000 - 80.000

A tiempo parcial

Hace 9 días
Generador de candidaturas

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Ventajas ofrecidas por este puesto de trabajo

Staff wellbeing program
24/7 Employee Assistance Program
Salary packaging benefits
Living expenses cap $9,010
Meals and entertainment cap $2,650

Descripción de la vacante

Barwon Health's Andrew Love Cancer Centre seeks aClinical Trial Coordinator to support current and upcoming haematology trials. You'll work with a multidisciplinary team to ensure high-quality data collection and successful trial management.

You will coordinate the delivery of trials, assist with participant education, and manage documentation in line with study protocols and ethical standards. This is a temporary part-time role supporting parental leave coverage.

Formación

  • Relevant degree in Nursing, Science, Health Science or related discipline.
  • Clinical trials experience is highly desirable.
  • Strong time management and communication skills are required.

Responsabilidades

  • Coordinate and deliver clinical trials at Andrew Love Cancer Centre, supporting recruitment, screening, enrolment, treatment and follow-up according to protocols.
  • Maintain high-quality trial data and documentation, including schedules, databases, adverse event reporting and data queries, adhering to ALCOA+ principles.
  • Build relationships with participants, families, investigators, sponsors and teams, providing clear trial information and education for participant safety and engagement.

Conocimientos

Time management
Attention to detail
Interpersonal skills
Communication skills
Data management

Educación

Nursing/Science/Health Science degree

Descripción del empleo

Barwon Health's Andrew Love Cancer Centre seeks aClinical Trial Coordinator to support current and upcoming haematology trials. You'll work with a multidisciplinary team to ensure high-quality data collection and successful trial management.

You will coordinate the delivery of trials, assist with participant education, and manage documentation in line with study protocols and ethical standards. This is a temporary part-time role supporting parental leave coverage.

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