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Clinical Research Associate Bridge Program Jobs in Texas

Neuralink

Clinical Research Associate

Austin, TX

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies. Your work will directly contribute to the planning, execution, and success of innovative ...

Neuralink

Clinical Research Associate

Austin, TX · On-site

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies. Your work will directly contribute to the planning, execution, and success of innovative ...

Becton, Dickinson and Company

Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ... Total Rewards program. We are committed to attracting and retaining high quality talent by ...

Neuralink

Clinical Research Associate

Austin, TX · On-site

$89K - $148K/yr

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies. Your work will directly contribute to the planning, execution, and success of innovative ...

Ascension

Clinical Research Associate

Austin, TX · On-site

... research records, including informed consents, case reports, clinical notes, and medical data ... disabilityEmployee assistance programs (EAP)Parental leave & adoption assistanceTuition ...

DiaSorin

Clinical Research Associate

Austin, TX

Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work associated with analytical and clinical studies conducted by Luminex, A DiaSorin Company for inclusion in ...

DiaSorin

Clinical Research Associate

Austin, TX · On-site

Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work associated with analytical and clinical studies conducted by Luminex, A DiaSorin Company for inclusion in ...

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All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Texas

Clinical Research Associate Bridge Program information

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How much do clinical research associate bridge program jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical research associate bridge program in Texas is $38.31, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $49.04 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate in a bridge program?

To thrive as a Clinical Research Associate in a bridge program, you need a foundational understanding of clinical trials, regulatory compliance, and data management, usually supported by a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, effective communication, and organizational skills help you manage study protocols and collaborate with diverse teams. These competencies are crucial for ensuring clinical trial integrity, regulatory adherence, and the successful execution of research studies.

What types of mentorship and training can I expect in a Clinical Research Associate Bridge Program?

Participants in a Clinical Research Associate (CRA) Bridge Program typically receive structured mentorship from experienced CRAs and clinical research professionals. The program often includes hands-on training in protocol review, site monitoring, regulatory compliance, and data management, combined with classroom or online learning modules. You'll work closely with cross-functional teams, such as clinical project managers and regulatory specialists, gaining exposure to industry-standard processes and tools. This supportive environment is designed to accelerate your transition into a CRA role and help you build a strong professional network within clinical research.

What is a Clinical Research Associate Bridge Program?

A Clinical Research Associate (CRA) Bridge Program is a specialized training course designed to help individuals transition into the role of a CRA, especially those with related experience in healthcare, life sciences, or clinical research support. These programs typically combine classroom instruction with practical training, focusing on topics such as clinical trial monitoring, regulatory compliance, and Good Clinical Practice (GCP) guidelines. The goal is to equip participants with the necessary knowledge and skills to begin a career as a CRA, often including job placement assistance or internships. Bridge programs are ideal for those who want to move into clinical research from a related field but lack direct CRA experience.

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Clinical Research Associate Bridge Program jobs near you
Infographic showing various Clinical Research Associate Bridge Program job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $79,695 per year, or $38.3 per hour.

Clinical Research Associate

Neuralink

Austin, TX

Full-time

Posted 17 days ago

Job description

Team Description:

The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what's possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink's BCI technology for use in people!

Job Description and Responsibilities:

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies. Your work will directly contribute to the planning, execution, and success of innovative trials, from the initial phases of study setup to hands-on clinical monitoring and site management. You'll be visiting sites both in-person and remotely to ensure protocol and regulatory compliance, tackle safety event management, and maintain essential documentation. Collaborating closely with a passionate, cross-functional team, as well as external partners, you'll be at the forefront of Neuralink's mission to push the boundaries of what's possible in clinical research. Additional job responsibilities will include:

  • Conduct site initiation, interim monitoring, and close-out visits (remote and on-site)
  • Ensure clinical studies are conducted in accordance with protocol, GCP, ISO 14155, and applicable regulatory requirements (e.g., 21 CFR Part 812)
  • Verify the accuracy, completeness, and consistency of clinical trial data through source data verification (SDV) and source data review (SDR)
  • Monitor participant safety by reviewing adverse events (AEs), serious adverse events (SAEs), and device deficiencies for completeness and timeliness
  • Ensure sites maintain adequate regulatory documentation, including Investigator Site Files (ISF), informed consent forms, and essential documents
  • Track site performance, enrollment, and data quality metrics; proactively identify risks and implement mitigation strategies
  • Support site training on protocol, investigational device use, and study procedures
  • Collaborate cross-functionally with Clinical Operations, Data Management, Regulatory, and Quality teams
  • Ensure timely resolution of data queries and protocol deviations
  • Prepare and maintain monitoring reports and follow-up letters in accordance with timelines
  • Support audit and inspection readiness at the site level

Required Qualifications:

  • Bachelor's degree in life sciences, engineering, or related field
  • 5+ years of clinical research experience (device experience strongly preferred)
  • Working knowledge of GCP (ICH E6), ISO 14155, and applicable FDA regulations
  • Experience with electronic data capture (EDC) systems and clinical trial documentation
  • Strong understanding of clinical trial processes, including monitoring and site management
  • Excellent communication, organization, and problem-solving skills
  • Ability to work independently in a fast-paced, evolving environment
  • Up to 30% travel (domestic and occasional international)

Preferred Qualifications:

  • Experience in neuromodulation, implantable devices, or other Class III medical devices
  • Experience supporting IDE or PMA clinical studies
  • Familiarity with risk-based monitoring approaches
  • Exposure to early feasibility or first-in-human studies
  • Exposure to market approval studies
  • Willingness and ability to travel up to 30-50% (domestic and occasional international)

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