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Internship Preclinical Study Monitor Jobs (NOW HIRING)

RPM ReSearch

Study Coordinator, Manager

Birmingham, AL · On-site

$80K - $110K/yr

... preclinical studies. You will play an instrumental role in optimizing workflows, monitoring financial impact, enhancing cross-functional processes, and elevating the quality of deliverables. This is ...

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How much do internship preclinical study monitor jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for internship preclinical study monitor in the United States is $15.54, according to ZipRecruiter salary data. Most workers in this role earn between $12.50 and $17.55 per hour, depending on experience, location, and employer.

What is an Internship Preclinical Study Monitor?

An Internship Preclinical Study Monitor is a trainee or entry-level professional who assists in overseeing preclinical studies, which are research experiments conducted before clinical trials in humans. Their responsibilities often include ensuring that laboratory procedures follow protocols, collecting and analyzing data, and maintaining accurate records. They work closely with research scientists and regulatory teams to ensure studies comply with ethical standards and regulatory requirements. This internship provides valuable hands-on experience in the field of biomedical research and drug development.

What are some typical responsibilities and learning opportunities for an Internship Preclinical Study Monitor?

As an Internship Preclinical Study Monitor, you will assist in overseeing preclinical studies to ensure they comply with regulatory standards and study protocols. Typical responsibilities include monitoring study progress, verifying data accuracy, coordinating with laboratory staff, and helping with documentation and reporting. This role offers valuable learning opportunities in Good Laboratory Practice (GLP) compliance, data management, and cross-functional collaboration with research scientists and quality assurance teams. Interns often gain hands-on experience in study monitoring and develop a deeper understanding of the drug development process, which can be beneficial for future roles in clinical research or regulatory affairs.

What are the key skills and qualifications needed to thrive as an Internship Preclinical Study Monitor, and why are they important?

To thrive as an Internship Preclinical Study Monitor, you need a foundational understanding of laboratory animal science, research methodologies, and data collection, often supported by coursework in biology or related fields. Familiarity with laboratory information management systems (LIMS), basic statistical software, and adherence to Good Laboratory Practice (GLP) guidelines are typically required. Attention to detail, strong organizational skills, and effective communication help interns excel in documenting results and collaborating with research teams. These competencies are vital for ensuring data integrity, regulatory compliance, and the successful completion of preclinical studies.

What is the difference between Internship Preclinical Study Monitor vs Clinical Research Coordinator?

AspectInternship Preclinical Study MonitorClinical Research Coordinator
CredentialsTypically pursuing or holding a degree in life sciences or related fieldOften holds a degree in health sciences, nursing, or related fields
Work EnvironmentLaboratories, preclinical research facilitiesClinical trial sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, biotech firms, research institutionsHospitals, clinical research organizations, academic medical centers
Search & Comparison IntentUnderstanding roles in preclinical research, internships, entry-level positionsManaging clinical trials, patient coordination, regulatory compliance

The Internship Preclinical Study Monitor focuses on overseeing preclinical experiments in labs, while a Clinical Research Coordinator manages clinical trials involving human participants. Both roles require related scientific credentials but differ in work environment and responsibilities, with the former centered on laboratory research and the latter on clinical trial management.

More about Internship Preclinical Study Monitor jobs
What cities are hiring for Internship Preclinical Study Monitor jobs? Cities with the most Internship Preclinical Study Monitor job openings:
What are the most commonly searched types of Preclinical Study Monitor jobs? The most popular types of Preclinical Study Monitor jobs are:
What states have the most Internship Preclinical Study Monitor jobs? States with the most job openings for Internship Preclinical Study Monitor jobs include:
Internship Preclinical Study Monitor jobs near you
Infographic showing various Internship Preclinical Study Monitor job openings in the United States as of July 2026, with employment types broken down into 3% Internship, 73% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $32,333 per year, or $15.5 per hour.

Preclinical Study Coordinator

Neuralink

Austin, TX • On-site

$31 - $53/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 29 days ago

Job description

About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Preclinical Team is responsible for designing, conducting, documenting, analyzing, and reporting preclinical studies. Our team provides a means for ensuring the safe, effective, and robust implantation of Neuralink devices into animals and, ultimately, humans.
Job Description and Responsibilities:
The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of day-to-day coordination, scheduling, data compilation, and administrative tasks, enabling the Study Director to focus on scientific oversight, data interpretation, and regulatory compliance. The Study Coordinator acts as a key liaison across the preclinical team, technical staff, and cross-functional groups to ensure studies progress smoothly, on time, and in compliance with protocols and SOPs. The Study Coordinator will:
  • Support the Study Director in developing study protocols, amendments, and related documentation.
  • Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings.
  • Identify and help eliminate roadblocks that could delay study progress.
  • Assist with implementation of test methods and practices described in the study protocol and SOPs.
  • Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified.
  • Manage the study schedule, alerting the Study Director and team to critical data collection points or deadlines.
  • Support the documentation and addressing of self-reported or QAU-generated deviations that may affect study quality.
  • Compile data, organize contributing scientist reports, and assist in preparing the final study report so it accurately reflects study results.
  • Maintain organized study files, track communications, and support archiving of data, documentation, protocols, specimens, and reports per GLP.
  • Coordinate day-to-day study activities with technical staff, veterinary teams, and external partners (e.g., CROs if applicable).
  • Contribute to internal tracking systems, meeting minutes, and status updates for the Preclinical Team.

Required Qualifications:
  • Bachelor's degree in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • Minimum 1 year of experience in preclinical research support, study coordination, or project management (academic experience applies).
  • Solid understanding of GLP regulations (21 CFR Part 58), basic knowledge of ISO 10993, and familiarity with in vivo animal studies.
  • Strong organizational and project management skills with proven ability to manage timelines and multiple priorities.
  • Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft Office (or equivalent) tools.
  • Experience working in or supporting animal research facilities with IACUC protocols.

Preferred Qualifications:
  • Master's degree in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • Direct experience with neural device implantation studies or neurosurgical models.
  • Background in a CRO or medical device preclinical setting.
  • Familiarity with electronic data capture systems or GLP-compliant documentation platforms.

Additional Requirements and Competencies:
  • Willingness to work in an animal research facility environment (with required training and PPE).
  • Flexibility in schedule to support critical study timepoints.

Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees' success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$31-$53 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
  • An opportunity to change the world and work with some of the smartest and most talented experts from different fields
  • Growth potential; we rapidly advance team members who have an outsized impact
  • Excellent medical, dental, and vision insurance through a PPO plan
  • Paid holidays
  • Commuter benefits
  • Meals provided
  • Equity (RSUs) *Temporary Employees & Interns excluded
  • 401(k) plan *Interns initially excluded until they work 1,000 hours
  • Parental leave *Temporary Employees & Interns excluded
  • Flexible time off *Temporary Employees & Interns excluded

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