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Who are we?
We’re Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980’s. If you already work in this industry you’ll know that we are experts in our field.

Why should you join Avance Clinical?
We appreciate that our most important asset is our people. We offer a fun, friendly work environment and a culture that values honesty and respect. We have a strong sense of team. We genuinely appreciate each individual but recognise the collective when achieving success.
We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.

Broad Purpose 
Avance Clinical is a Contract Research Organisation which offers specialised services supporting drug development for the pharmaceutical and biotechnology industry. 
 
The Clinical Research Associate III (CRA III) performs activities associated with the evaluation, initiation, monitoring and close out of clinical trials to ensure the trial is conducted in accordance with the protocol; company Standard Operating Procedures (SOPs), ICH GCP guidelines and other applicable regulatory requirements. 
 
Core Responsibilities  

• Conduct site and investigator feasibility activities. 
• Develop study-related documents or plans under the supervision of the study Project Manager.  
• For a multi-site study, oversee and lead the operations of the clinical team as the Lead CRA including development of Clinical Monitoring Plan, study-specific annotated report, reviewing Visit Reports.  
• Perform all activities (preparation, execution and follow-up) associated with onsite or remote Pre-Study Visits (PSV), Study Initiation Visits (SIV), Dose Witness Visits (DWV), Interim Monitoring Visits (IMV) and Close-out Visits (COV).  
• Generate and maintain high quality confirmation letters, site visit reports, follow-up letters and other documentation related site monitoring and management to ensure compliance with ICH GCP, study protocol and regulatory requirements.  
• Monitor participant source data, review Investigator Site Files (ISF), perform Investigational Product accountability, meet with site personnel and ensure procedures are conducted in accordance with the protocol and ICH GCP.  
• Perform protocol review as requested.  
• Raise data queries in the Case Report Form (CRF) where discrepancies are identified and work with site staff to ensure timely and accurate resolution.  
• Collect TMF documentation from site and ensure accurate and timely filing as per SOP requirements.  
• Maintain effective site communication to proactively manage on-going study expectations and issues.  
• Participate in study-specific or vendor audits conducted by sponsors or regulatory agencies, and respond to audit observations, as required.  
• Ensure Serious Adverse Events are reported (initial and follow-up) as per protocol requirements.  
• Provide guidance and mentoring to less experienced staff during co-monitoring visits and facilitating accompanied site visits.  
• Other duties as directed by Line Management or delegate in line with skills, experience and/or qualifications 

 
Departmental Responsibilities  

• Foster the on-going commitment to maintaining a healthy team culture and promoting good morale, by actively participating in regular Clinical Operations Team meetings.  
• Maintain effective communication with other members of the department.  
• Proactively identify risks related to departmental service provision and assist in their mitigation and resolution.  
• Manage and track business related expenses as per company policy. 
• Assist with the development of departmental SOPs as required. 
• Participate in internal Quality Assurance activities as required, including responding to internal audit findings. 

 
Qualifications, Skills and Experience 

• Bachelor's level degree in life sciences, pharmacy, nursing or equivalent field.  
• Previous experience as a CRA in a CRO or Pharma Company for at least 2 years. 
• Formal ICH GCP training and a working knowledge of ICH GCP Guidelines and other applicable regulatory requirements.  
• Clear understanding of the requirement to adhere strictly to client confidentiality.  
• Effective written and oral communications skills, including the ability to keep clients, senior management and other stakeholders informed of project updates and other pertinent information.  
• Demonstrated ability to take initiative in problem solving and in exercising. good judgment.  
• Awareness of Privacy Legislation as it applies to the Clinical Trial environment.  
• Ability to work under pressure in a multi-disciplinary team environment.  
• Willingness to work in, and be supportive of, a positive and dynamic team culture.  
• Ability to travel. Moderate level of interstate travel may be required (up to 50%).  

What we offer

• Stimulating work
• Project diversity
• An intellectual challenge
• An agile & flexible workplace
• Opportunity to progress
• Stability
• Sense of community
• A leadership team that are working together on a common goal
• Flexible work options
• Great tools / tech to do your job

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