Clinical Research Coordinator - Nurse / Pharmacist

Paratus Clinical; Brisbane; On-site; AUD 55,000 - 69,000; Full time

Job summary

Paratus Clinical Research Brisbane is seeking a Clinical Research Coordinator (Nurse or Pharmacist) to join our team on a casual onsite basis from January to March with the opportunity to continue beyond this period. The role balances clinical tasks with administration across multiple trials and offers a flexible, collaborative team environment.

Successful candidates will be AHPRA registered or a licensed Pharmacist, vaccinated for COVID-19 and influenza, and comfortable using EMR systems and

Qualifications

• AHPRA Registered Nurse or licensed Pharmacist.
• Vaccination experience and eligible for COVID-19/Influenza vaccination.
• Ability to work independently and within a collaborative team, with strong time management.
• Experience with clinical trials and GCP is desirable.

Responsibilities

• Adhere to protocols, ethical and regulatory requirements and GCP guidelines for trials.
• Manage and coordinate participants throughout the study.
• Preparation, dispensing and administration of investigational product.
• Study-related data entry - source, CRF and site file management.
• Work with the study team, including ethics, recruitment, coordinators and Investigators.

Skills

Excellent communication

Strong organisational skills

Team player

Education

AHPRA Registered Nurse

Registered Pharmacist

Tools

EMR systems

Clinical databases

Job description

Clinical Research Coordinator (Nurse or Pharmacist) - Casual

Availability required from January to March, with the opportunity to continue in an ongoing casual role beyond this period.

Tired of shift work and looking for a change? Interested in gaining experience working in Clinical Trials? Paratus Clinical Research Brisbane is looking for a Clinical Research Coordinator (Nurse or Pharmacist) to join our team on a casual basis. The role provides a great balance between clinical and administrative tasks in a variety of clinical research studies. You will be part of a collaborative team that offers flexibility and opportunities to rapidly develop skills and experience.

Paratus Clinical is a network of high-quality private clinical trial sites, established to meet the increasing need for efficient, cost-effective and quality delivery of clinical trials within Australia particularly in the primary care setting. Sitting outside of the Public Health system, we pride ourselves on our responsiveness to client needs with the speed and quality of the delivery of our client's clinical trials.
Our mission is to become the provider of choice for many pharmaceutical companies around the world to deliver their clinical trial for new and novel therapies in areas such as vaccine research, dermatology, rheumatology, haematology, asthma, diabetes, pain, high cholesterol, obesity and many more therapeutic areas.

The Role:

The role is casual and is onsite.

The role includes, but is not limited to the following:

• Adhere to protocols, ethical and regulatory requirements and GCP guidelines at all times for assigned trials
• Manage and coordinate participants throughout the study
• Preparation, dispensing and administration of the investigatory product
• Study-related data entry - source, CRF and site file management
• Work with the study team, including ethics, recruitment, coordinators and Investigators

About you:

You are a team-oriented professional with excellent communication skills and a strong background in health sciences or relevant clinical research experience. You are confident using a variety of software applications, databases, and electronic medical records. Most importantly, you embody our values: Resilience, Quality, Responsibility, and Collaboration.

Essential Criteria

• AHPRA Registered Nurse / Pharmacist
• Vaccination experience
• Ability to work both independently and within a collaborative team
• Strong organisational skills and high attention to detail
• Effective time management, with the ability to prioritise and meet deadlines
• Flexible, adaptable, and strong problem-solving abilities
• Vaccinated for COVID-19 and seasonal Influenza

Desirable Criteria

• Knowledge of GCP, regulatory requirements, ethics, privacy, and other relevant guidelines
• Experience as a Coordinator on commercially sponsored clinical trials
• Venepuncture experience