×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Research Project Manager - Project

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Senseye
Full Time position
Listed on 2026-07-10
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 123000 - 149000 USD Yearly USD 123000.00 149000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Project Manager - Project Hire

About Us

Senseye is a Neuro Technology Company in Austin, TX, on the cusp of revolutionizing Mental Health. Over the past six years, we have invested millions of dollars in R&D to build our platform, allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases, we are now focused on building the world’s first Objective Mental Health Diagnostics on top of our core technology.

Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform that gives clinicians a safe and objective, accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for millions of sufferers.

The Senseye platform could be the technology that drives this change. This is an excellent opportunity to shape the future of digital medicine and address unmet medical needs that affect billions of people worldwide.

What we are looking for:

This is a fixed-term project role through the completion of our Phase III tirial. Strong performers may be considered for permanent positions as the team grows. This role will be responsible for managing Senseye as a virtual site in the Phase III study. Experience in site management, particularly in a virtual or decentralized model is required. The anticipated duration of the project is expected to be between 6-12 months.

The Clinical Research Project Manager is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

By performing these duties, the CRC works with the PI and internal teams to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

Responsibilities
  • Oversee all aspects of Senseye's virtual site for the Phase III trial
  • Schedule, screen and perform study visits
  • Implement, and manage clinical trials from start to finish, including providing input to protocol development, patient enrollment, and data analysis.
  • Serve as the primary liaison between the company, clinical investigators, and regulatory agencies to ensure compliance with all federal, state, and institutional regulations.
  • Develop and maintain trial timelines, budgets, and resources, adjusting as necessary to meet project milestones.
  • Train and supervise junior clinical research staff, ensuring adherence to study protocols and regulatory requirements.
  • Prepare and submit regulatory documents, such as IRB applications, informed consents, and progress reports, ensuring timely approval and compliance.
  • Collaborate with cross-functional teams, including R&D, Quality Assurance, and Product, to ensure seamless integration of clinical research findings into product development and marketing strategies.
  • Analyze and interpret clinical data, preparing detailed reports and presentations for internal and external stakeholders.
  • Stay abreast of industry trends, regulatory updates, and emerging technologies in software as a medical device (SaMD) research, applying best practices to enhance trial efficiency and effectiveness.
To succeed in this role, you should have the following skills and experience
  • Bachelor’s degree in a life sciences or related field
  • Minimum of 5 years of experience in clinical research coordination, preferably in the medical device industry, with a proven track record of successful trial management.
  • Experience managing a clinical research site(s), particularly in a virtual or decentralized trial model
  • Comprehensive understanding of FDA regulations, ICH GCP guidelines, and other applicable regulatory requirements.
  • Exceptional organizational, leadership, and problem-solving skills.
  • Strong…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary