20 Best Research Scientist 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: $29.6K - $37.5K a year
Quick Apply
Research Scientist
SOLAREA BIO, INC —Waltham, MA
The research scientist should detect consequential knowledge gaps, formulate comprehensive research strategies, and then execute rigorous methodological and…
Estimated: $96.1K - $122K a year
Quick Apply
2d
Research Audiologist
Boys Town —Omaha, NE
Have or be eligible for appropriate state licensing. Engaging in efforts to educate the community about science.
Estimated: $58.5K - $74K a year
Scientist - BioPharma LC-MS/MS
KCAS Bio —Olathe, KS
Bachelor’s degree in Chemistry, Biochemistry or chemical/biochemical engineering, or related field with at least 3 years of experience with LC-MS/MS OR.
$70,000 - $110,000 a year
Quick Apply
RN Clinical Compliance Manager
BrightStar Care of Santa Barbara County —Santa Barbara, CA
Registered Nurse (RN) with a valid state license. Online trainings available that qualify for license renewal requirements. Assist with skilled nursing intake.
$114,400 - $124,000 a year
Quick Apply
Research and Development Manager
Ahead Human Resources —Louisville, KY
Assist in budgeting product development and field trial efforts. The employee will also assist with multiple field trials and the subsequent management and…
$80,000 - $100,000 a year
Quick Apply
Mobile Clinical Research Phlebotomist - Douglas, AZ
ViTalent, LLC —Douglas, AZ
Must have previous blood draw experience. Minimum of two years of blood draw experience. Specimen collection, processing, packaging, and shipping.
Estimated: $53K - $67.2K a year
Quick Apply
12d
Psychometrician
Yvonne B. Reedy, Ph.D Psychological and Counseling Associates —Philipsburg, PA
Masters Degree in Psychology or related field. The Psychometric Technician will manage psychological testing inventories and materials and will administer and…
Estimated: $38.2K - $48.3K a year
Quick Apply
6d
Computational Scientist
ADNET Systems, Inc. —Hampton, VA
FUN3D is a CFD suite of tools developed by NASA to study and develop new algorithms for unstructured grid fluid dynamic simulations spanning incompressible flow…
Estimated: $118K - $149K a year
Quick Apply
Medical Lab Scientist I
Sonora Quest —Fallon, NV
Where no certification is available from a certifying agency, a bachelor’s degree with one year of experience in that discipline is required.
Senior Toxicologist
Battelle —West Jefferson, OH
Diplomate of the American Board of Toxicology certified OR DABT eligible - if not already certified, candidate will be required to become board certified within…
Estimated: $110K - $139K a year
Laboratory Technician
GenoTyping Center of America —Waterville, ME
We use the latest technological innovations in genetic analysis to provide laboratory tests that have a significant impact on the progress of basic and…
From $14.15 an hour
Quick Apply
13d
ANALYTICAL LABORATORY RESEARCH SCIENTIST
Prosolus, Inc. —Miami, FL
You will be responsible for the design and development of brand-new analytical testing methodologies and improvements to existing test methods and processes…
Estimated: $79.9K - $101K a year
Quick Apply
R&D Formulation Manager
American Regent, Inc. —Brea, CA
Provide technical leadership for the design and execution of Quality-by-Design (QbD) product development studies and development of scalable manufacturing…
$132,800 - $145,000 a year
Scientist 3 - Clinical Research
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
Responsible for the translation and implementation of (non-medical) scientific concepts into the study design and/or program across planning, execution, and…
Estimated: $102K - $129K a year
Quick Apply
11d
Research Assistant
Foundation for Law and International Affairs —Remote
Summarize key academic work and practical information in the field; Completion of bachelor’s degree or current enrollment in a master’s program required, master…
Estimated: $46.1K - $58.4K a year
Quick Apply
Applications Scientist
SciAps, Inc. —Andover, MA
Provide feedback to R&D and Product Management to further develop and optimize these approaches to produce higher performing instrumentation that exceeds our…
$60,000 - $90,000 a year
Quick Apply
Business Attraction and Investment Manager, CRA
City of Dania Beach —Dania Beach, FL
If the driver’s license is out of state, must be able to obtain a Florida driver’s license within thirty (30) days of the hire date.
$66,181.32 - $102,580.95 a year
General Research Science
Heirloom Carbon —Brisbane, CA
Experience using basic hand and power tools safely. Position may require working at heights including; climbing ladders/equipment, stairs, elevators, and…
$95,000 - $195,000 a year
Quick Apply
Beamline Scientist
Brookhaven National Laboratory —Upton, NY
Ph.D. in materials science, chemistry, physics, environmental science or a related field. Develop an independent science program and work as member of a team to…
$101,200 - $184,000 a year
3d

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Research Assistant

Ophthalmology Specialists of Texas - Abilene, TX

Quick Apply

Job Details

Full-time Estimated: $29.6K - $37.5K 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

Research Scientist jobs

Research Assistant

Research Scientist

Research Audiologist

Scientist - BioPharma LC-MS/MS

RN Clinical Compliance Manager

Research and Development Manager

Mobile Clinical Research Phlebotomist - Douglas, AZ

Psychometrician

Computational Scientist

Medical Lab Scientist I

Senior Toxicologist

Laboratory Technician

ANALYTICAL LABORATORY RESEARCH SCIENTIST

R&D Formulation Manager

Scientist 3 - Clinical Research

Research Assistant

Applications Scientist

Business Attraction and Investment Manager, CRA

General Research Science

Beamline Scientist

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