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
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 Coordinator
Allegheny Health Network —Erie, PA
Driver's license may be required depending on facility requirements. Current research-related certification from accredited program such as The Association of…
Estimated: $56.5K - $71.6K a year
Clinical Research Coordinator Lead
Allegheny Health Network —Pittsburgh, PA
Driver's license may be required depending on facility requirements. Bachelor’s Degree in biology, nursing, healthcare or closely related field.
Estimated: $69.2K - $87.7K a year
Senior Clinical Research Associate
Everest Clinical Research —Remote
Must maintain a valid driver’s license and be able to drive to monitor sites. Bachelor’s degree in a Life Science or related field of study.
Estimated: $110K - $139K a year
Quick Apply
3d
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
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
Clinical Research Coordinator
NEXTSTAGE CLINICAL RESEARCH LLC —Waco, TX
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information,…
$45,000 - $75,000 a year
Quick Apply
1h
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
Research Nurse Coordinator
Baptist Health System KY & IN —Lexington, KY
Under limited supervision, coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol…
Estimated: $55.4K - $70.2K 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
Quick Apply
8d
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
XBiotech USA, Inc —Austin, TX
RN or BA/BS degree in clinical, science or health related field. Contributes to site level recruitment strategy and contingency planning and implementation in…
Estimated: $69.1K - $87.5K a year
Quick Apply
4d
RESEARCH OPHTHALMIC ASSISTANT
Vance Thompson Vision Clinic Prof L —Sioux Falls, SD
Serving as the primary liaison between clinical study sponsors, patients, and VTV staff regarding study protocol requirements and communicates clinical study…
Estimated: $40.1K - $50.8K a year
Quick Apply
RN- Clinical Oncology Research Coordinator- 40 hours- day shifts
Henry Ford Health —Detroit, MI
Current valid Michigan RN license required. OCN certification required within three (3) years of hire into the position. ACRP or SOCRA certification preferred.
$35.10 - $46.92 an hour
Quick Apply
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: $51.2K - $64.9K a year
Quick Apply
5d
Clinical Research Associate - SMNJ Research
Saint Michaels Medical Center —Newark, NJ
Responsibilities: Under the direction and supervision of the Director of Research, this position facilitates all implementation phases of new studies as well as…
3d
RN Clinical Research Coordinator - Cardiology - Full Time
Sanford Health —Sioux Falls, SD
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
2d
Clinical Research Associate (CRA/Senior CRA for In-House Opportunity)
San Francisco —San Francisco, CA
Chair or participate in meetings or conference calls with multi-disciplinary study team, regional monitors, or vendors (e.g., CROs, central Labs).
$130,000 - $150,000 a year
Quick Apply
Clinical Research Coordinator
Mission Cancer + Blood —Des Moines, IA
Answer telephone, screen calls, take messages, and provide information to appropriate staff. Participate in presentations or seminars related to the field of…
Estimated: $46.2K - $58.5K a year
Quick Apply
5d

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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

Senior Clinical Data Manager

Clinical Research Coordinator

Clinical Research Coordinator Lead

Senior Clinical Research Associate

Clinical Research Associate

RN Clinical Research Coordinator - Full Time

Clinical Research Coordinator

Clinical Research Assistant

Research Nurse Coordinator

Clinical Research Assistant/Medical Assistant

Research Assistant I - Center of Excellence on Mood Disorders

Clinical Research Associate

RESEARCH OPHTHALMIC ASSISTANT

RN- Clinical Oncology Research Coordinator- 40 hours- day shifts

Clinical Research Coordinator

Clinical Research Associate - SMNJ Research

RN Clinical Research Coordinator - Cardiology - Full Time

Clinical Research Associate (CRA/Senior CRA for In-House Opportunity)

Clinical Research Coordinator

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