ZipRecruiter

Log In

1

Research Study Jobs (NOW HIRING)

CARTI, Inc.

Research Study Coordinator II

Little Rock, AR · On-site

$23.25 - $31/hr

Description The Clinical Research Study Coordinator executes and coordinates daily clinical research activities according to Good Clinical Practice (GCP) and FDA/ICH guidelines; completes ...

CARTI, Inc.

Research Study Coordinator II

Little Rock, AR

$23.25 - $31/hr

The Clinical Research Study Coordinator executes and coordinates daily clinical research activities according to Good Clinical Practice (GCP) and FDA/ICH guidelines; completes International ...

next page

Showing results 1-20

People also search for

All JobsResearch Study Jobs

Research Study information

See salary details

$8

$34

$85

How much do research study jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for research study in the United States is $34.40, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $39.66 per hour, depending on experience, location, and employer.

What is a Research Study job?

A Research Study job involves conducting investigations to gather, analyze, and interpret data on a specific topic. Professionals in this role design experiments, collect information from various sources, and summarize findings to contribute to scientific or academic knowledge. They may work in universities, healthcare, corporate research, or government agencies. Responsibilities can include literature reviews, data collection, statistical analysis, and report writing.

What are the key skills and qualifications needed to thrive in the Research Study position, and why are they important?

To succeed in a Research Study position, you typically need strong analytical skills, attention to detail, and a background in scientific or social science research methodology—usually supported by a relevant degree. Familiarity with data analysis software like SPSS, R, or Python, as well as experience with survey tools and ethics certifications (such as CITI training), is frequently required. Excellent written and verbal communication, organization, and collaboration skills set top candidates apart. These competencies are crucial for accurately collecting, analyzing, and presenting data while working effectively within multidisciplinary research teams.

What are the typical daily responsibilities of someone working in a Research Study role?

Daily responsibilities in a Research Study role often include collecting and managing data, recruiting and coordinating with study participants, and maintaining accurate documentation of research activities. You may also be involved in designing study protocols alongside lead researchers, analyzing results using statistical software, and preparing progress reports or manuscripts for publication. Collaboration is common, as you'll work closely with principal investigators, research assistants, and sometimes external partners. Attention to detail and strict adherence to ethical standards are important in ensuring reliable and valid study outcomes.
More about Research Study jobs
What cities are hiring for Research Study jobs? Cities with the most Research Study job openings:
What are the most commonly searched types of Research Study jobs? The most popular types of Research Study jobs are:
What states have the most Research Study jobs? States with the most job openings for Research Study jobs include:
What job categories do people searching Research Study jobs look for? The top searched job categories for Research Study jobs are:
Research Study jobs near you
Infographic showing various Research Study job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 92% Full Time, 6% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $71,549 per year, or $34.4 per hour.
Clinical Research Study Manager

Clinical Research Study Manager

DM Clinical Research

Jersey City, NJ

Full-time

Posted 23 days ago

Job description

Clinical Research Study Manager
A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. In addition, ensure study enrollment meets or exceed Sponsors' expectations and company goals are achieved on a timely basis.
DUTIES amp; RESPONSIBILITIES
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA certifications on a timely basis.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
  • Adherence and compliance to the assigned protocols at their respective site(s).
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to
  • Sponsor-provided and IRB-approved Protocol Training
  • All relevant Protocol Amendments Training
  • Any study-specific Manuals Training as applicable
  • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate and timely follow-up on the action items, at their respective site(s).
  • Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocols at their respective site(s).
  • Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
  • Creating and or Reviewing Source Documents for their assigned protocol(s) at their respective site(s) in a timely manner.
  • Responsible for training the site teams and supporting the adequate conduct of study subject visits, and all other relevant protocol required procedures and documenting these in a timely manner.
  • Responsible for enforcing ALCOA-C Standards with all the relevant clinical trial documentation.
  • Responsible for enforcing all Adverse and Serious Adverse Events reporting and any other relevant Safety Information reporting to the appropriate authorities per internal company guidelines, Sponsor, IRB and ICH-GCP Guidelines.
  • Ensuring data quality, subject retention and compliance, and timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
  • Working with the cross-functional team(s) and site team(s) to ensure study start readiness on all the aspects and adequate training completed by all the relevant site staff prior to FPFV and continue working with the cross-functional team(s) for the successful execution and completion of the clinical trial.
  • Responsible for clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs and guidance documents.
  • Working closely with the Associate Site Director/Site Director to achieve strategic goals for the site.
  • Assist the Associate Site Director/Site Director with staff training and any other relevant tasks assigned.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Strive to ensure weekly, monthly and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
  • Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
  • Facilitate effective communication between patients, healthcare providers, and research staff
  • Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
  • Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
  • Facilitate effective communication between patients, healthcare providers, and research staff
  • Any other matters as assigned by management.
KNOWLEDGE amp; EXPERIENCE
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree preferred
  • Foreign Medical Graduates preferred
Experience:
  • Minimum of 5 years experience in Clinical Research
  • Supervisory experience preferred
  • Wide therapeutic range of clinical trials experience preferred
  • Regulatory research experience is a plus
Credentials:
  • ACRP or equivalent certification is preferred
Knowledge and Skills:
  • Goals-driven while continuously maintaining quality.
  • Must be detailed-oriented, proactive, and able to take initiative.
  • Must have strong written and communication skills.
  • Must have excellent customer service skills.
  • Proficient communication and comprehension skills both verbal and written in the English language are required.
  • Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.

Apply