Top 17042 Study coordinator Jobs

Preclinical Study Coordinator
Neuralink —Austin, TX
- $31 - $53 an hour
- Full-time
- Master's degree
- Bachelor's degree
- 1 year
- Commuter assistance
- Paid holidays
Clinical Study Coordinator
City of Hope —Duarte, CA
- $44.90 - $69.60 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
Central Study Coordinator- Retention
Care Access —Boston, MA
- $65,000 - $75,000 a year
- Remote
- Spanish
- Computer literacy
- Writing skills
- Health savings account
- Paid holidays
Study Coordinator - CSTS
Henry M. Jackson Foundation —Bethesda, MD
- $25.38 - $30.00 an hour
- Full-time
- Hybrid work
- Psychiatry
- Mid-level
- Leadership
- Health insurance
- Dental insurance
Study Coordinator
Franklin Bio Lab —King of Prussia, PA
- Full-time
- Current TB test
- Writing skills
- Mid-level
- Health savings account
- AD&D insurance
Quick Apply
Study Coordinator
Howard University —Washington, DC
- $50,000 - $60,000 a year
- Full-time
- Word processing
- Bachelor of Science
- English
- 403(b) matching
- Commuter assistance
Study Coordinator
INOTIV BOULDER LLC —Boulder, CO
- $27 - $34 an hour
- Overtime
- Microsoft Outlook
- Mid-level
- Math
- Paid parental leave
- Disability insurance
Quick Apply
11d
Research Assistant (Remote with travel)
Centricity Research —Remote
- Full-time
- Mid-level
- Travel
- In-person
- Continuing education credits
- Paid holidays
Quick Apply
Clinical Research Coordinator I - Medicine
Henry M. Jackson Foundation —Bethesda, MD
- Full-time
- University
- Entry level
- Health insurance
- Dental insurance
Assistant Clinical Research Coordinator - Pediatrics
UCLA Health —Los Angeles, CA
- $29.28 - $47.10 an hour
- Word processing
- Computer literacy
- University
- Flexible schedule
Study Coordinator
Rocky Mountain Cancer Centers —Denver, CO
- $60,000 - $75,000 a year
- Background check
- Pass drug screening
- Mid-level
- Wellness program
- Health savings account
Regulatory Coordinator I - Study Activation
Johns Hopkins All Children's Hospital —Saint Petersburg, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Research Recruitment Coordinator
Betting Hero —Remote
- Remote
- Google Workspace
- Administrative experience
- Continuous improvement
Quick Apply
14d
Clinical Research Coordinator
Oura —Remote
- $65,450 - $90,000 a year
- Remote
- Mid-level
- Office
- 1 year
- Paid holidays
- Health insurance
3d
Contractor (6 Months) Study Coordinator (equivalent level to RA)
Editas Medicine —Cambridge, MA
- $40 - $45 an hour
- Contract
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
Research Coordinator
Catholic Health —Roslyn, NY
- $32 - $50 an hour
- Medicine
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Tuition reimbursement
Clinical Study Coordinator
Milestone One —Cleveland, TN
- Full-time
- CPR Certification
- BLS Certification
- Mid-level
Quick Apply
R-112413 Clinical Research Recruitment Coordinator
Carbon Health Technologies Inc —California
- $0 a year
- Part-time
- Remote
- Mid-level
- Fair chance
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Mid-level
- High school diploma or GED
- University
PRODUCT/DRUG SAFETY COORDINATOR AND CODING SPECIALIST
Zenith LifeScience —South Plainfield, NJ
- $60,000 - $70,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- 1 year

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Preclinical Study Coordinator

Neuralink -
Austin, TX

Apply Now

Job Details

Full-time
$31 - $53 an hour

Benefits

Commuter assistance
Paid holidays
Health insurance
Dental insurance
401(k)
RSU
Parental leave
Vision insurance

Qualifications

Research project management
Institutional Animal Care and Use Committees (IACUCs) guidelines compliance
Bachelor's degree
Biomedical regulatory compliance
Managing projects
Research regulatory compliance
Productivity software
Personal Protective Equipment (PPE)
FDA regulations

Full 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.

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

Apply Now

Refine Your Search

study coordinator jobs

Preclinical Study Coordinator

Clinical Study Coordinator

Central Study Coordinator- Retention

Study Coordinator - CSTS

Study Coordinator

Study Coordinator

Study Coordinator

Research Assistant (Remote with travel)

Clinical Research Coordinator I - Medicine

Assistant Clinical Research Coordinator - Pediatrics

Study Coordinator

Regulatory Coordinator I - Study Activation

Research Recruitment Coordinator

Clinical Research Coordinator

Contractor (6 Months) Study Coordinator (equivalent level to RA)

Research Coordinator

Clinical Study Coordinator

R-112413 Clinical Research Recruitment Coordinator

Clinical Research Coordinator

PRODUCT/DRUG SAFETY COORDINATOR AND CODING SPECIALIST

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