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: $32.4K - $41K a year
Quick Apply
Postdoctoral Trainee
Catalight —Walnut Creek, CA
We follow a training model of structured skill development that entails didactic training, group and individual supervision, shadowing, skill acquisition,…
$80,000 a year
Research RN
South Denver Cardiology Associates —Littleton, CO
Valid RN license from the State of Colorado. The Clinical Research Nurse, under the guidance and supervision of the Principal Investigator (PI), ensures the…
$30.12 - $32.50 an hour
Quick Apply
14d
Clinical Research Site Manager
Texas Diabetes & Endocrinology, P.A. —Round Rock, TX
This person will answer staff questions regarding clinical trials and general office concerns. Provides a safe environment for patients, families, and clinical…
From $50,671.80 a year
Quick Apply
Fermentation Research Scientist, Team Leader
Trait Biosciences —Santa Fe, NM
You have a graduate degree (PhD preferred) in microbiology, biochemical engineering, biotechnology, fermentation engineering, or a related field.
From $100,000 a year
Quick Apply
1h
Remote Research Interviewer - Part Time
Escalent —Nashville, TN
Type 20 wpm w/ 85% accuracy. Training is scheduled to begin Thursday July 18, held remotely, on a group video call. You must have reliable WIFI service to use.
Estimated: $34K - $43.1K a year
Quick Apply
4d
Clinical Research Coordinator
ObjectiveHealth —Akron, OH
The ideal candidate will possess certification such as an RN, LPN, MA, phlebotomy, or similar, prior clinical research experience, and have a strong desire to…
Estimated: $47.1K - $59.7K a year
Quick Apply
14d
Research Director
Neuro Behavioral Research, Inc —North Canton, OH
Market research: 1 year (Preferred). \*\*Education:\*\* Master’s degree preferred, but not required. \*\*Competitive Salary starting at 100k per year based on…
From $100,000 a year
Quick Apply
Research Scientist (inorganic material)
Epic Advanced Materials —Westlake Village, CA
Graduate degree in Chemistry, Materials Science, Chemical Engineering, or a closely related field. You will work closely with senior scientists to design and…
$80,000 - $100,000 a year
Quick Apply
6d
Research Scientist (Virologist)
Pharmgate Biologics, Inc —Saint Paul, MN
The ability to prioritize, develop and implement research plans that are aligned with corporate priorities; proven ability to balance multiple, and often…
$70,000 - $90,000 a year
Quick Apply
Medical Researcher
Clinical Research Center of Florida —Pompano Beach, FL
You will make a base salary of $50,000.00($25.00 per hour) and opportunity for bonuses based on performance.
$24 - $25 an hour
Quick Apply
6d
Research Scientist - Oncology Immunotherapy
Pathfinder Oncology, Inc. —Raleigh, NC
Plan, design, optimize, and oversee the execution of experiments focused on oncology immunotherapy, including the development of novel immunotherapeutic agents,…
From $130,000 a year
Quick Apply
7d
Receptionist (Brown Center - Research)
Care New England —Providence, RI
Job Summary: The receptionist is responsible for screening and directing all telephone calls and mail deliveries. Adheres to appropriate security procedures.
Estimated: $56.8K - $71.9K a year
Quick Apply
5d
Senior Food Scientist
STEVEN CHARLES —Aurora, CO
Provide and communicate technical and business risk assessment and perspective. Support the process design and review on new capability expansion, cost…
$80,000 - $100,000 a year
Quick Apply
Manager, Clinical Pathology
Altasciences —Auxvasse, MO
Skilled in hematology, cytology, chemistry, urinalysis, and coagulation assays with previous proven experience in a clinical pathology laboratory.
Estimated: $58K - $73.4K a year
7d
Senior Research Scientist, Outcomes Research Network
Edward-Elmhurst Health —Evanston, IL
Expected to serve as a Principal Investigator/Program Director for own externally funded projects while also leveraging their research contributions as co…
Estimated: $103K - $130K a year
Application Scientist - Methane Emissions
Heath Consultants, Inc. —Houston, TX
The candidate will also play a leading role in data collection in the field using instruments to measure Ch4 and other related gases and provide analysis.
$90,000 - $115,000 a year
Quick Apply
Research Scientist, PRIOR
The Allen Institute for AI —Seattle, WA
A strong foundation (typically PhD level) in one or more of the following areas: natural language processing, machine reading, automatic knowledge base…
$167,030 - $260,570 a year
Quick Apply
2d
Biotrial Clinical Pharmacology Unit Director - Clinical Research
Biotrial, Inc. —Newark, NJ
The ideal candidate will have a Doctoral degree (MD, DO) with an active license to practice medicine in New Jersey. Clinical operations: 5 years (Preferred).
Estimated: $151K - $192K a year
Quick Apply
AI Research Residency Program
Prime Intellect —Remote
Collaborate with leading experts in AI, distributed systems, and protocols to develop state-of-the-art open language models, coding agents, and scientific…
Estimated: $79K - $100K a year
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

Research Scientist jobs

Research Assistant

Postdoctoral Trainee

Research RN

Clinical Research Site Manager

Fermentation Research Scientist, Team Leader

Remote Research Interviewer - Part Time

Clinical Research Coordinator

Research Director

Research Scientist (inorganic material)

Research Scientist (Virologist)

Medical Researcher

Research Scientist - Oncology Immunotherapy

Receptionist (Brown Center - Research)

Senior Food Scientist

Manager, Clinical Pathology

Senior Research Scientist, Outcomes Research Network

Application Scientist - Methane Emissions

Research Scientist, PRIOR

Biotrial Clinical Pharmacology Unit Director - Clinical Research

AI Research Residency Program

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