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