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Research Staff Jobs (NOW HIRING)

Brown University Health

Research Supv PD

Providence, RI · On-site

$35.90 - $59.23/hr

Selects, orients, schedules, assigns work and evaluates performance of subordinate research staff. Ensures implementation of approved research program, adherence to research protocols, development ...

Brownhealth

Research Supv PD

Providence, RI · On-site

Selects, orients, schedules, assigns work and evaluates performance of subordinate research staff. Ensures implementation of approved research program, adherence to research protocols, development ...

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

... research staff communication. Responsibilities include managing study documentation, overseeing site-specific trial activities, and ensuring adherence to regulatory and sponsor requirements.

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Research Staff information

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$22K

$64.1K

$93.5K

How much do research staff jobs pay per year?

As of Sep 8, 2026, the average yearly pay for research staff in the United States is $64,055.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $83,000.00 per year, depending on experience, location, and employer.

What is research staff?

Research staff are professionals who support and conduct research projects within organizations such as universities, research institutes, or private companies. Their roles can include designing experiments, collecting and analyzing data, managing laboratory equipment, and assisting principal investigators with grant writing and publications. Research staff may hold titles such as research assistant, research associate, or laboratory technician. They play a crucial role in advancing scientific knowledge and ensuring that research projects are carried out efficiently and ethically.

What are the key skills and qualifications needed to thrive as research staff?

To thrive as Research Staff, you typically need strong analytical abilities, attention to detail, and a relevant academic background such as a bachelor's or master's degree in the field. Familiarity with data analysis software (e.g., SPSS, R, or Python), laboratory equipment, or research management systems is often required. Excellent organization, effective communication, and critical thinking are standout soft skills for this role. These competencies ensure rigorous research processes, high-quality data, and successful collaboration within research teams.

What are some common challenges faced by research staff when managing multiple projects simultaneously?

Research Staff often juggle several projects at different stages, which can make prioritizing tasks and meeting deadlines challenging. Effective time management and clear communication with team members and supervisors are crucial to ensure progress on all fronts. Utilizing project management tools and regularly updating stakeholders helps balance responsibilities, reduce stress, and maintain high-quality research outputs.

What is the difference between Research Staff vs Research Associate?

AspectResearch StaffResearch Associate
Required CredentialsBachelor's or Master's degree, sometimes PhD for senior rolesBachelor's or Master's degree, often entry-level
Work EnvironmentLaboratories, research centers, academic institutionsLaboratories, academic settings, industry research teams
Employer & Industry UsageUniversities, government agencies, private R&DUniversities, research institutes, corporate labs
Common Search & Comparison IntentUnderstanding roles, qualifications, career pathEntry-level research roles, job responsibilities

Research Staff typically hold more advanced degrees and may have more responsibilities in project management or specialized research. Research Associates are often entry-level or early-career roles focused on supporting research activities. Both roles are common in academic and industry research settings, but Research Staff generally require more experience or qualifications.

What are popular job titles related to Research Staff jobs?

For Research Staff jobs, the most frequently searched job titles are:

Research Staff jobs near you
Infographic showing various Research Staff job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, and 5% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $64,055 per year, or $30.8 per hour.

Senior Clinical Research Coordinator

Tekton Research Inc

Austin, TX • On-site

$100 - $125/hr

Other

Posted 26 days ago

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Senior Clinical Research Coordinator

Full Time Austin, TX, US

7 days ago Requisition ID: 1133

Senior Clinical Research Coordinator - Austin, Texas

Full-Time/Non-Exempt/On-Site

Position Summary

The Senior Clinical Research Coordinator (Senior CRC) is an experienced clinical research professional responsible for managing multiple clinical trials from study start-up through close-out. This role ensures protocol compliance, participant safety, data integrity, regulatory compliance, and successful study execution.

The Senior CRC serves as a key liaison between investigators, sponsors, monitors, participants, and research staff while providing guidance and mentorship to junior coordinators. The ideal candidate is highly organized, proactive, detail-oriented, and able to effectively manage multiple priorities.

Key Responsibilities
  • Independently coordinate and manage multiple clinical trials from start-up through close-out.
  • Serve as a primary site contact for investigators, sponsors, monitors, vendors, and study teams.
  • Recruit, screen, consent, enroll, and retain study participants according to protocol requirements.
  • Conduct study visits and perform pediatric and adult phlebotomy and specimen processing as required.
  • Monitor participant safety and appropriately document and report adverse events and protocol deviations.
  • Maintain accurate source documentation, regulatory files, and essential study records in compliance with GCP, FDA regulations, and ICH guidelines.
  • Prepare and submit IRB and regulatory documents, including amendments and continuing reviews.
  • Maintain accurate study data in EDC and CTMS systems and resolve data queries within required timelines.
  • Prepare for and support monitoring visits, sponsor audits, and regulatory inspections.
  • Identify and resolve study issues proactively to maintain timelines, quality, and compliance.
  • Mentor and provide guidance to Clinical Research Coordinators and other research staff.
  • Contribute to process improvement and overall site quality and performance.
Required Qualifications
  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, Clinical Research, or related field preferred.
  • 3-5+ years of clinical research experience, with demonstrated ability to independently coordinate clinical trials.
  • Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical research processes.
  • Experience managing multiple clinical trials and competing priorities.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with EDC systems, CTMS, and Microsoft Office.
  • Strong organizational, problem-solving, and communication skills.
  • Ability to work independently, exercise sound judgment, and collaborate effectively with multidisciplinary teams.
  • Commitment to participant safety, data integrity, and research quality.
Preferred Qualifications
  • Current ACRP orCCRC, or equivalent certification.
  • Bachelor's or advanced degree in a healthcare, public health, or clinical research field.
  • Experience with industry-sponsored and/or multi-center clinical trials.
  • Experience mentoring junior research staff.
  • Experience supporting sponsor audits, regulatory inspections, or complex monitoring activities.
  • Experience with participant recruitment and retention strategies.
Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We value professional development, collaboration, accountability, and meaningful contributions.

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