20 Best Clinical 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: $29.6K - $37.5K a year
Quick Apply
RN Clinical Research Coordinator - Full Time
Sanford Health —Fargo, ND
Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and/or possess multistate licensure if in…
$27.50 - $44.00 an hour
Quick Apply
3d
Inhouse Clinical Research Associate
Novotech —United States
Relevant experience/qualifications in Life Sciences or related field or administration would be preferable. Update and maintain site milestones including EC/HA…
Estimated: $68.9K - $87.3K a year
Patient Recruitment & Clinical Research Associate
Piomic Medical AG —Remote
Participate and occasionally lead regularly scheduled update calls with study sites. Work closely with clinical team members to develop and fulfill patient…
$75,000 - $100,000 a year
Quick Apply
3d
Clinical Research Assistant
NEXTSTAGE CLINICAL RESEARCH LLC —Eau Claire, WI
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information,…
From $15 an hour
Quick Apply
2d
Senior Clinical Data Manager
Celldex Therapeutics, Inc. —New Haven, CT
Initiate CRF development for new clinical trials and protocol amendments; collaborate with internal team and responsible vendor on CRF development, database…
Estimated: $107K - $135K a year
Clinical Research Assistant/Medical Assistant
Alliance for Multispecialty Research, LLC —Lexington, KY
Assist in general office work flow which includes telephone answering. O Answering and triage of research office calls. O Filing and pulling study records.
From $20 an hour
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8d
Clinical Research Assistant Coordinator
Connecticut Eye Consultants, P.C. —Danbury, CT
Position involves informing participants about clinical trials, conducting protocol visits, corresponding with study partners (sponsor, IRB, CRO, etc...),…
Estimated: $38.8K - $49.1K a year
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Senior Clinical Trial Manager
BioPhase —San Diego, CA
Prepare/review site study documents (i.e., site-specific informed consent, study tools/worksheets, investigator contracts, and site payments).
$155,000 - $165,000 a year
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Clinical Trial Associate
Spectrum Staffing Services —Hopewell, NJ
Supports management and maintenance of filing systems for non-TMF documentation. The maintenance and management of assigned sites IRB initial submissions.
$70,000 a year
Research Assistant I - Center of Excellence on Mood Disorders
UTHealth Houston —Houston, TX
Research activities may include some or all of the following: communication with industry sponsors, patient recruiting and screening, traditional laboratory…
Estimated: $38.5K - $48.7K a year
4d
Clinical Research Associate - Sponsor Dedicated
IQVIA —Remote
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and…
Estimated: $65.5K - $82.9K a year
Clinical Research Coordinator
Essential Medical Research, LLC —Tulsa, OK
BS/BA in life sciences, biology, or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g., clinical research…
$40,000 - $55,000 a year
Quick Apply
Clinical Research Coordinator
Allegheny Health Network —Pittsburgh, PA
Driver's license may be required depending on facility requirements. Current research-related certification from accredited program such as The Association of…
Estimated: $56.4K - $71.4K a year
Clinical Research Associate II
ProSciento, Inc —United States
Must be able to drive and have a valid driver’s license. University/college degree (life science preferred), or certification in a related allied health…
$100,000 - $125,000 a year
Quick Apply
Research Associate
Diverge Translation Science Laboratory, LLC —Milwaukee, WI
Conduct a wide variety of protein analysis assays and data analysis independent of supervision in support of research and clinical trial related studies.
$52,000 - $63,000 a year
Quick Apply
4d
Clinical Research Associate
Clinical Research Center of Florida —Miami 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
2d
Clinical Research Associate
Cliantha Research —Remote
Bachelor's degree in a relevant field such as Life Sciences or Nursing(Prefered). Collaborate with clinical laboratory staff to coordinate sample collection and…
$70,902 - $80,522 a year
Quick Apply
Clinical Research Coordinator/Medical Assistant
Alliance for Multispecialty Research —Newton, KS
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
Up to $24 an hour
Quick Apply
4d
Clinical Research Coordinator/Ophthalmic Technician
Eye Associates, PLLC —San Antonio, TX
Over 1 year experience in either ophthalmic technician or clinical research coordination. Coordinate and oversee clinical research studies from initiation to…
Estimated: $35.5K - $45K a year
Quick Apply

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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

Clinical Research Associate jobs

Research Assistant

RN Clinical Research Coordinator - Full Time

Inhouse Clinical Research Associate

Patient Recruitment & Clinical Research Associate

Clinical Research Assistant

Senior Clinical Data Manager

Clinical Research Assistant/Medical Assistant

Clinical Research Assistant Coordinator

Senior Clinical Trial Manager

Clinical Trial Associate

Research Assistant I - Center of Excellence on Mood Disorders

Clinical Research Associate - Sponsor Dedicated

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Associate II

Research Associate

Clinical Research Associate

Clinical Research Associate

Clinical Research Coordinator/Medical Assistant

Clinical Research Coordinator/Ophthalmic Technician

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