Senior Clinical Trials Site Lead – Growth & Impact

i-Pharm Consulting; Sydney; Presencial; AUD 70.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary and benefits

Professional development opportunities

Collaborative work environment

Contribution to cutting-edge clinicalp

Descripción de la vacante

i-Pharm Consulting is seeking an experienced Clinical Trials Site Study Coordinator to oversee day-to-day operations of clinical trials in the Illawarra region. You will ensure regulatory compliance and deliver high-quality care to study participants, coordinating activities from initiation to completion.

The role requires a Life Sciences degree and at least 2 years of experience in clinical trials coordination, with strong knowledge of GCP and excellent communication skills to liaise with

Formación

• Bachelor's degree in Life Sciences or related field is required.
• Minimum 2 years of experience in clinical trials coordination or similar role.
• Strong understanding of clinical trial processes and regulations (GCP).
• Excellent communication and interpersonal skills; able to work independently and in a team.

Responsabilidades

• Coordinate and manage clinical trial activities from initiation to completion.
• Obtain informed consent from study participants and safeguard their rights and well-being.
• Schedule and conduct study visits and document data accurately.
• Maintain study records and databases with up-to-date information.
• Communicate effectively with investigators, sponsors, and regulatory bodies.
• Ensure compliance with GCP and regulatory guidelines; assist in protocol and report preparation; provide training as needed.

Conocimientos

CTMS

EDC systems

GCP knowledge

Communication

Teamwork

Educación

Bachelor's degree in Life Sciences

Herramientas

CTMS

EDC

Descripción del empleo

i-Pharm Consulting is seeking an experienced Clinical Trials Site Study Coordinator to oversee day-to-day operations of clinical trials in the Illawarra region. You will ensure regulatory compliance and deliver high-quality care to study participants, coordinating activities from initiation to completion.

The role requires a Life Sciences degree and at least 2 years of experience in clinical trials coordination, with strong knowledge of GCP and excellent communication skills to liaise with