Senior Clinical Trial Study Coordinator

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

How refreshing it is to hear of an organisation that will prioritise working on the best studies, with the best sponsors first?

How does it make you feel that an organisation wants to mentor and prepare you for developing within a business that is experiencing exponential growth?

This leading Clinical Research Site based in the major regional hub in the Illawarra area conducting innovative and impactful clinical trials to improve patient outcomes. The collaborative environment offers the perfect setting for professionals passionate about making a difference in healthcare.

We are seeking an experienced and motivated Clinical Trials Site Study Coordinators to oversee the day-to-day management of these clinical trials. You will play a crucial role in ensuring the smooth operation of the studies, maintaining compliance with regulatory requirements, and providing exceptional care to study participants.

• Coordinate and manage clinical trial activities from initiation to completion.
• Obtain informed consent from study participants and ensure their rights and well-being are protected.
• Schedule and conduct study visits, including the collection and documentation of data.
• Maintain accurate and up-to-date study records and databases.
• Communicate effectively with study investigators, sponsors, and regulatory bodies.
• Ensure compliance with Good Clinical Practice (GCP), ethical standards, and regulatory guidelines.
• Assist in the preparation of study protocols, reports, and other documentation. Provide training and support to study staff and participants as needed.

Required

• Bachelor's degree in a related field (e.g., Nursing, Life Sciences, or equivalent)
• Minimum of 2 years of experience in clinical trials coordination or a similar role
• Strong understanding of clinical trial processes
• Effective communication and interpersonal skills
• Ability to work independently and as part of a team
• Proficiency in using CTMS and EDC systems

On offer

• Competitive salary and benefits package
• Opportunities for professional development and career advancement
• A supportive and collaborative work environment
• The chance to contribute to cutting-edge clinical research and improve patient outcomes.