20 Best Research Assistant jobs (Hiring Now!)

Research Assistant
Ophthalmology Specialists of Texas —Abilene, TX
Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all…
Estimated: $32.4K - $41K a year
Quick Apply
Associate Director of Laboratory Finance
Vanderbilt University Medical Center —Nashville, TN
Supports VUMC initiatives impacting lab including proforma financial analysis, development of internal pricing models, supporting managed care rate negotiations…
Bilingual Research Assistant/Community Health Worker
Matthew Walker Comprehensive Health Center —Nashville, TN
Bachelors’ degree from an accredited college or university in Marketing, Health Promotions/Outreach, Health Education, health administration or related field,…
Estimated: $34.1K - $43.2K a year
Quick Apply
Clinical Research Assistant
NEXTSTAGE CLINICAL RESEARCH LLC —Eau Claire, WI
The working environment consists of an indoor and climate-controlled setting the majority of the time, and with frequent exposure to a healthcare clinical…
From $15 an hour
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11d
Quality Laboratory Technician
Grassland Dairy Products, Inc. —Greenwood, WI
Our Grassland Lab Technicians are responsible for the designated analysis of any environmental and/or incoming/outgoing product to ensure that specification is…
From $21 an hour
Research Assistant (Division of Research) 24D
Women & Infants Hospital —Providence, RI
Clinical or technical research experience, including data collection, chart abstraction and data entry into MS Access desired.
Estimated: $65.9K - $83.4K a year
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8h
Research & Development Tech for Baked Goods
The Raymond Hadley Corporation —Spencer, NY
The R&D Technician is responsible for driving product innovation through the research and development of products that align our capabilities with new and…
$16 - $18 an hour
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RN Cardiac Cath Lab Tech
Cone Health —Greensboro, NC
In addition, personnel are expected to function and provide high quality, safe, culturally competent cost effective patient care in all areas of operations by…
Estimated: $69.7K - $88.3K a year
Metallurgical Laboratory Technician
United Technical —Whitmore Lake, MI
Our certified laboratory staff consists of AWS CWI and Welding Engineers which work with all materials and welding processes. Must be able to lift 50 lbs.
Estimated: $37.4K - $47.4K a year
Quick Apply
Clinical Research Assistant
Essentia Health —Duluth, MN
2 years of post high school education including completion of college level curriculum in a healthcare related field. Over 1 year computer database experience.
Estimated: $44.3K - $56.2K a year
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11h
Clinical Research Coordinator
CenExel iResearch —Decatur, GA
Bachelor's Degree or equivalent experience in Clinical Research or related field. O Responsible for timely data entry and query resolution.
Estimated: $45.8K - $58K a year
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Research Assistant I
DLH —Durham, NC
Supports study team in receiving and responding to participant communications through telephone calls, mailings, and emails.
$58,000 - $68,000 a year
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20h
Cath Lab Tech Hiring Event
HCA Florida Sarasota Doctors Hospital —Sarasota, FL
One (1) to three (3) years’ experience in licensed field and one (1) year cardiac cath lab interventional experience preferred.
Research Assistant
Pandemic Relief Supply —San Francisco, CA
The ideal candidate will assist in various research projects and experiments, contributing to the advancement of scientific knowledge.
$25 - $40 an hour
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6d
Research Assistant
Children's Minnesota —Minneapolis, MN
Proficiency in Microsoft Office tools (Word, Excel, PowerPoint, Teams); including database and mainframe software and research measurement tools.
$32,864 - $54,288 a year
Quick Apply
6d
Dental Lab Technician
Aspen Dental —Thomaston, ME
Our best-in-class training program, competitive compensation, and flexible scheduling will help you thrive in your career. Paid time off and holidays.
$32 - $36 an hour
11d
Research Associate / Compensation Analyst -- Part Time & Remote
SmithPilot Inc. —Remote
Preparing exhibits of data/research for client delivery. This is a part-time, remote, contract position, approximately 10 to 20 hours per week (generally…
$50 - $75 an hour
Quick Apply
6d
Cardiac Catheterization Laboratory Tech
Grand View Health —Sellersville, PA
Vocational diploma from an accredited school of Cardiovascular Science required, or vocational diploma from an AMA-approved radiologic technology program and…
Estimated: $72.8K - $92.1K a year
Research Assistant II
CenExel IResearch LLC —Decatur, GA
Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks. Timely completion of data entry and query resolution for all CRFs, based on…
Estimated: $31.3K - $39.6K a year
Quick Apply
13d
Data Research Assistant
Panum Aviation Consulting LLC —Bethesda, MD
Proficient in data entry and typing. Knowledge of pivot tables, vlookups and sumifs for data manipulation and analysis. Shows creativity in problem solving.
$20 - $23 an hour
Quick Apply

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Research Assistant

Ophthalmology Specialists of Texas - Abilene, TX

Quick Apply

Job Details

Full-time Estimated: $32.4K - $41K a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

English
High school diploma or GED
Organizational skills
Clinical trials
Good Clinical Practice
Associate's degree
Medical terminology
FDA regulations
Time management

Full Job Description

POSITION SUMMARY

The Research Assistant is responsible for helping the Study Coordinator in the coordination and implementation of clinical protocols from pre-study planning through the successful completion of patient visits and documentation.

ESSENTIAL FUNCTIONS

Practices with ethical and legal guidelines

Assist the Research Coordinate in the coordination of studies according to ICH and GCP guidelines as specified in the protocol

Assists in the daily clinical trial activities and plays a critical role in the conduct of the study.

Assists in the Scheduling of study participant appointments and serves as the patient liaison to the PI and other participating physicians.

Reviews and comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.

Working closely with the PI, participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols open to enrollment. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.

Coordinates and facilitates monitoring and auditing visits. Notifies appropriate ICR officials of external audits by IRB’s, Regulatory agencies, CRO’s and sponsors.

Collaborates with PI and ICR to respond to any audit findings and implement-approved recommendations.

Coordinates and attends sponsor prequalification visits, monitor visits, study termination visits.

Completes case report forms. Extracts data from patient charts in a timely manner

Responds to data clarification requests in a timely manner.

May attend Investigator meetings requiring travel and report pertinent information back to research team members.

Coordinates with PIs to help ensure that clinical research and related activities are performed in accordance with Federal regulations, ICR and sponsoring agency policies and procedures.

Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains records and other documentation of training.

Maintains subject screening logs and protocol deviation logs.

Completes documentation on each study visit that is used to track all study related activities so that time, effort and materials can be accounted for on a monthly basis.

Ensures that all materials for each clinical trial protocol are available for subject enrollment.

Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data.

Performs specimen processing and shipment of biological specimen duties.

Assists with study materials including but not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.

Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required.

Assists the Principal Investigator in submission of accurate and timely closeout documents to applicable Federal agencies, and the sponsoring agency in accordance with Federal regulations and institutional policies and procedures.

Arranges secure storage of study documents that will be maintained according to SCRG institutional policy or for the contracted length of time, whichever is longer.

Promotes the ethical conduct of research by reporting good faith suspicions of misconduct in research to the Director of Research

May perform other job related duties as requested or required

REQUIRED SKILLS

Ability to work with other research team members and have strong organizational and time management skills

Strong critical thinking and problem solving skills

Ability to work under pressure

Dependable

Exercises safe judgment in decision making

Demonstrates tact and understanding when dealing with patients, team members, members of other disciplines, and the public

Must possess honesty, integrity, and accountability

Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors.

Knowledge of medical terminology.

Knowledge of good clinical practice, FDA, OHRP, HIPAA policies.

Previous work with CRFs and EDC.

Excellent organizational skills to independently manage work flow.

Ability to prioritize quickly and appropriately.

Ability to multi-task.

Meticulous attention to detail

WORK ENVIRONMENT

The Research Study Coordinator will work primarily in an office setting; some travel required to satellite locations and outside meetings (see TRAVEL).

PHYSICAL DEMANDS

Must be able to move intermittently throughout the workday

Must be able to speak and write the English language in an understandable manner

Requires repetitive hand motion

Minimal lifting and carrying requirements

TRAVEL

Minimal travel to satellite locations and outside meetings

DIRECT REPORTS

None

REQUIRED EDUCATION/EXPERIENCE

High school diploma or GED

PREFERRED EDUCATION/EXPERIENCE

Associate Degree in Science.

CERTIFICATIONS

COA preferred

Job Type: Full-time

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Schedule:

Monday to Friday

Experience:

relevant: 1 year (Preferred)

Work Location: In person

Quick Apply

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Clinical Research Assistant

Clinical Research Coordinator

Research Assistant I

Cath Lab Tech Hiring Event

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Research Assistant

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Research Associate / Compensation Analyst -- Part Time & Remote

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