Senior Clinical Research Associate at ProPharma

Melbourne, Victoria, Australia -

Full Time

Start Date

Immediate

Expiry Date

03 Aug, 26

Salary

0.0

Posted On

05 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Monitoring, Source Data Verification, ICH-GCP, Regulatory Compliance, Trial Master File Maintenance, Clinical Trial Processes, Communication, Organization

Industry

Business Consulting and Services

Description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. Job Title: Clinical Research Associate (CRA) – 0.2 FTE Location: New South Wales (NSW) or Melbourne, Australia About the Role We are seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join our team on a 0.2 FTE (one day per week equivalent) basis. This is an excellent opportunity for an experienced CRA looking for flexible, part-time work while contributing to high-quality clinical research projects. Key Responsibilities Conduct site monitoring visits (remote and on-site as required) in accordance with study protocols, ICH-GCP, and regulatory requirements Ensure data integrity and compliance through source data verification (SDV) Build and maintain strong relationships with investigational sites Support site initiation, monitoring, and close-out activities Identify and escalate risks or issues impacting study delivery Assist with regulatory document review and maintenance of Trial Master Files (TMF) Collaborate with cross-functional teams to ensure smooth study execution About You Previous experience as a Clinical Research Associate (or similar role) Strong understanding of ICH-GCP guidelines and clinical trial processes Excellent communication and organisational skills Ability to work independently with minimal supervision Located in NSW or Melbourne, with willingness to travel occasionally if required Relevant degree in life sciences, nursing, or a related field preferred #LI-LH1 We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Don’t see an open opportunity that matches your qualifications? Join our talent community to stay connected for potential future opportunities. Upload your resume/CV and contact details for our Talent Acquisition team to review and match for potential future opportunities. While you are here, sign up for Job Alerts to receive alerts of future opportunities that match your selected interests. To change the language, click on "English" at the top right corner of the screen and select your preferred language. If you are already signed in, click the cloud icon and go to Change Language. ProPharma will never ask you for any bank account information, financial information, or another form of payment to be considered for a role. Additionally, the ProPharma talent acquisition team will only use their work email addresses (domain@propharmagroup.com). If you receive recruiting communications from anyone with a yahoo.com, gmail.com, live.com, propharmagroupjobs.com, or any other email account, it’s likely a fraud. Are you currently a ProPharma colleague? To be considered for an opportunity, please apply through the Jobs Hub in Workday.

Responsibilities

The role involves conducting remote and on-site monitoring visits to ensure data integrity and compliance with study protocols. Responsibilities include managing site relationships and supporting initiation, monitoring, and close-out activities.