20 Best research associate 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
Assistant Vice President for Research Integrity
Texas A&M University Corpus Christi —Corpus Christi, TX
The AVPRI is ultimately responsible for the effectiveness of the Office of Research Integrity's programs, as measured by TAMU-CC's ability to successfully…
Estimated: $100K - $127K a year
Associate Scientist - HPLC , TOC , GMP - 3rd Shift Monday through Friday 11:00pm - 7:30am
Alcami —North Charleston, SC
While performing the duties of this job, the employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; fumes or airborne…
Estimated: $48.4K - $61.3K a year
Quick Apply
Research Assistant - Hybrid Research
RiceTec, Inc. —Alvin, TX
The successful candidate should have a bachelor’s degree in Agriculture or related field. Perform layout of fields for planting the yield trials, prepare seed…
Estimated: $42.8K - $54.2K a year
Associate Food Scientist
Dairyfood USA, Inc. —Blue Mounds, WI
Understanding what they need and our ability to quickly and profitably develop or match processed and plant based cheeses is the cornerstone of our business and…
$60,000 - $75,000 a year
Quick Apply
PLS Associate Scientist I
Pace® —Oakdale, MN
A proven history of effective communication (verbal, written, and visual) with technical and non-technical. Continuously drives strategic department improvement…
Estimated: $47.1K - $59.6K a year
Research Associate I, Pharmacology
UTMB Health —Galveston, TX
Sets up and conducts standard research experiments following detailed technical instructions. Prepares biological assays and conducts basic quantitative and…
Estimated: $45.1K - $57.2K a year
3d
Associate Scientist - Pharma LC-MS/MS
KCAS Bio —Olathe, KS
Act as lead scientist, help to design experiments, provide work instructions and technical training to more junior scientific staff in daily activities.
$62,500 - $68,500 a year
Quick Apply
Administrative Assistant - Research Department
Caron Treatment Centers —Wernersville, PA
Review data for errors in entry. Demonstrate attention to detail through a minimum of errors in data entry. Schedule patient research appointments into Aura and…
Estimated: $37.5K - $47.5K a year
Quick Apply
12d
Post Doctoral Research Associate
Lifespan —Providence, RI
Under the general supervision of the Principal Investigator, and within established policies and procedures, performs scientific investigative research;…
$61,008 - $74,088 a year
Quick Apply
4d
Research Associate - Discovery Core (Contract)
Vertex Pharmaceuticals —San Diego, CA
Bachelor's degree in biology or a related field and 1+ years experience in a research laboratory. Performs initial analysis of experimental data and interprets…
$27 - $30 an hour
Research Associate - AAV Packaging
Avista Therapeutics Inc —Pittsburgh, PA
A Bachelor's degree and three years of professional experience or a Master's degree (Master's degree preferred) in Molecular Biology, Neurobiology, Genetics, or…
$65,000 - $75,000 a year
Quick Apply
11d
Research & Development Technician
Watchfire Signs LLC —Danville, IL
This position will support all the engineering groups within R&D in various technical and functional aspects of research and development of new products and…
$65,000 - $75,000 a year
Quick Apply
Legal Research & Writing - Associate Attorney
Kubicki Draper —Miami, FL
Must be an active member of the Florida Bar. An active member of the Florida Bar in good standing, Required. Assist with Drafting Appellate Briefs.
Estimated: $85.7K - $109K a year
Quick Apply
Research Associate
UT Health Science Center at San Antonio —San Antonio, TX
Under general supervision, responsible for performing technical or narrative research by designing, modifying and collaborating with primary investigator…
1d
Communications and Research Associate
The Negev Foundation —Cleveland, OH
Proficiency in social media platforms and content creation. Podcast Coordination: *Your responsibilities will include promoting and marketing podcast episodes…
$45,000 - $55,000 a year
Quick Apply
Clinical Research Assistant-PRN
NEXTSTAGE CLINICAL RESEARCH LLC —Tulsa, OK
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information,…
$25 - $35 an hour
Quick Apply
RESEARCH ASSOCIATE
Cumberland Heights Foundation Inc —Nashville, TN
Conduct literature reviews to inform study design, measure selection, analysis design, and outcome measures. Master’s or doctorate degree in a mental or public…
Estimated: $56.2K - $71.2K a year
Quick Apply
10d
DMPK Research Associate/Sr. (Contract) 22019
Vertex Pharmaceuticals —San Diego, CA
Bachelor’s degree (B.A./B.S.) or equivalent degree in a biological science. While the research facility is not a Good Laboratory Practices (GLP) compliant…
$35 - $40 an hour
11d
Research Associate
MilliporeSigma —Tamaqua, PA
1+ years of science or technical industrial experience. A strong technical understanding of fundamental analytical chemistry.
2d

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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
GCP
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 associate jobs

Research Assistant

Assistant Vice President for Research Integrity

Associate Scientist - HPLC , TOC , GMP - 3rd Shift Monday through Friday 11:00pm - 7:30am

Research Assistant - Hybrid Research

Associate Food Scientist

PLS Associate Scientist I

Research Associate I, Pharmacology

Associate Scientist - Pharma LC-MS/MS

Administrative Assistant - Research Department

Post Doctoral Research Associate

Research Associate - Discovery Core (Contract)

Research Associate - AAV Packaging

Research & Development Technician

Legal Research & Writing - Associate Attorney

Research Associate

Communications and Research Associate

Clinical Research Assistant-PRN

RESEARCH ASSOCIATE

DMPK Research Associate/Sr. (Contract) 22019

Research Associate

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