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Senior Clinical Research Associate -Australia

Synchron Inc. -
Melbourne VIC

Quick Apply

Job Details

Full-time
$120,000 - $140,000 a year

Benefits

Commuter assistance
Health insurance
Unlimited annual leave
Dental insurance
Annual leave
Life insurance

Qualifications

Patient monitoring
Microsoft Office
Master's degree
Bachelor's degree
Organisational skills
Communication skills

Full Job Description

About Synchron

Synchron’s vision is to build non-surgical brain–computer interfaces at global scale that protect the fundamental human rights of freedom of expression and autonomy. Our first mission is to develop motor decoders that restore the ability of 15 million people with paralysis to interact with the digital world. Our second mission is to develop whole-brain cognitive decoders that enable hundreds of millions of people with cognitive decline to preserve and expand their agency as cognition changes over time. In pursuing these goals, we aim not only to help humans flourish, but also to drive fundamental discoveries in human intelligence. Our team operates at the intersection of healthcare and technology, translating breakthrough research into real-world, safety-critical systems.

Senior Clinical Research Associate -Australia

Location: Melbourne, Australia
Work Arrangement: In the field
Type: Full-time

About the Role

The Senior Clinical Research Associate will play a crucial role in the set-up and execution of groundbreaking studies. This position will be a self-starter, reporting to the Sr. Director Clinical Operations, focusing on the study start-up and in-country infrastructure from the initial phases of study set-up to hands-on clinical monitoring and site management.

Key Responsibilities

Conduct qualification, initiation, monitoring, and closeout visits at research sites in accordance with approved protocol(s), GCP, SOPs, and applicable regulatory requirements.
Complete monitoring visit reports and visit letters that includes complete summaries and accounts of onsite activities.
Verify medical record and source documentation against case report form (CRF) data, including informing the site staff of any entry errors, ensuring good documentation practices (GDP) are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory regulations.
Ensure RGO submissions and approvals are in place, to include applicable regulatory documentation with proactive follow-through to ensure site readiness and study progress.
Follow-up with clinical sites on all open action items, collection of essential records, RGO submissions/approvals, and subject status
Serve as the primary operational liaison between Synchron and investigative sites, focused on study conduct, protocol execution, data integrity, and patient safety.
Verify adequate investigator qualifications, training resources, sufficient study staff, and appropriate investigator oversight.
Contribute to the development of case report forms , informed consent documents, and other essential trial documentation.
Support tracking and reporting study progress including site performance and data collection.
Assist with ensuring proper documentation, audit readiness, and inspection compliance
Ensure adherence to GCP-ICH guidelines and applicable regulatory requirements.
Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement as well as helping with Sponsor recruitment activities.

Required Qualifications

Bachelor’s or Master’s degree in Life Sciences or related field.

Minimum 6 years of clinical research experience, with at least 4 years of onsite monitoring.
Strong understanding of local clinical research regulations, GCP-ICH guidelines, regulations, and compliance requirements (e.g. 21 CFR 812, ISO14155).
Requires exceptional self-direction and initiative! Must independently identify, prioritize, and execute on opportunities without prompting.
Proven ability to multi-task, prioritize workload effectively, and meet deadlines in a fast-paced environment.
Excellent interpersonal, communication, and organizational skills with a high affinity for collaboration.
Results driven and effective at working at all levels of an organization.
Clear and concise in verbal and written communication.
Ability to travel domestically, as required, >60% during peak times

Preferred Qualifications

Experience with medical devices, neurology, neuromodulation or Brain Computer Interface (BCI) trials.
Experience monitoring a Class III implantable device
Proficiency in Microsoft Office Suite
Familiarity with EDC, TMF and CTMS systems.
Experience working in a fast-paced medical device startup environment (preferred)

Compensation

The base salary range for this role is $120,000 – $140,000AUD depending on experience, skills, and qualifications.

In addition to base salary, this role may be eligible for discretionary bonuses and/or equity grants, subject to board approval and company policy.

Visa Sponsorship

We are unable to offer visa sponsorship for this position at this time.

Benefits (for W-2, full-time, exempt employees in the US only) ***Intern positions not eligible

Subsidized medical and dental insurance coverage for you and your dependent(s)
Life insurance, short-term disability, long-term disability
401k
Discretionary unlimited PTO
Flexible Spending Account for you and your dependent(s), with eligible plan elections
Commuter benefits for NY employees

Equal Employment Opportunity (EEO)

Synchron is an equal opportunity employer. We are committed to creating an inclusive environment for all employees and applicants and provide equal employment opportunities without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable law.

If you need a reasonable accommodation during the application or interview process, please let us know.

Join Us

At Synchron, you will be part of a transformative mission and you will work alongside driven people who believe in the power of collaboration and innovation to make a lasting impact. If you are excited to stretch your skills and contribute to something meaningful, apply and now and build the future with us.

Quick Apply

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