20 Best Clinical Research Associate jobs (Hiring Now!)

Clinical Research Coordinator, RN
Wichita Urology Group —Wichita, KS
The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials.
From $50,000 a year
Quick Apply
6d
Clinical Research Coordinator
CenExel iResearch —Decatur, GA
Bachelor's Degree or equivalent experience in Clinical Research or related field. O Responsible for timely data entry and query resolution.
Estimated: $45.8K - $58K a year
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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
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9d
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
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11d
Lead Clinical Research Coordinator
Folio Clinical Research —Murrieta, CA
Bachelor's degree or equivalent combination of education/experience in science or health-related field. Ensuring appropriate communication and ongoing oversight…
$65,000 - $85,000 a year
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4d
Clinical Research Coordinator
Memorial Health System —Effingham, IL
A bachelor's degree in nursing or other health-related field is preferred. Corrects and resubmits data or answers queries within one week of receipt or as…
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11d
Experienced Clinical Research Coordinator
California Liver Research Institute —Pasadena, CA
The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials.
From $25 an hour
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Oncology Clinical Research Associate - IQVIA Biotech
IQVIA —Remote
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and…
$87,200 - $145,300 a year
12h
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
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Clinical Research Coordinator
Virginia Urology —Richmond, VA
A bachelor’s degree in biology, biochemistry, psychology, engineering, computer science, mathematics or other applied science is strongly preferred.
Estimated: $46.2K - $58.5K a year
Quick Apply
4d
Clinical Research Coordinator PRN
NEXTSTAGE CLINICAL RESEARCH LLC —Eau Claire, WI
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information,…
$25 - $35 an hour
Quick Apply
11d
Assistant Director – Pre-Award Clinical Trials (Vanderbilt Ingram Cancer Center)
Vanderbilt University Medical Center —Nashville, TN
Problem Solving/ Complexity of work: Integrate knowledge and in-depth analysis from several areas to resolve complex problems that are both technical and…
RN Clinical Research Coordinator - Phase 1 Oncology - 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
23h
Clinical Research Coordinator (local recruits only)
Las Vegas Medical Research —Las Vegas, NV
Collaborating closely with principal investigators to coordinate all aspects of research studies, from participant recruitment and eligibility assessment to…
$27 - $33 an hour
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Senior Clinical Research Coordinator
Early Access Care LLC —Madison, CT
BS/BA, education required preferably in a health-related, life science area or technology-related field or equivalent combination of education, training, and…
$105,000 - $150,000 a year
Quick Apply
Clinical Research Assistant
East-West Medical Research Institute —Honolulu, HI
Ideal candidates will possess Bachelor's degree in the sciences and/or clinical experience. Employee will be trained to follow Good Clinical Practices and…
$18 - $23 an hour
Quick Apply
Clinical Research Assistant
Colorado Springs Urological Associates PLLC —Spokane, WA
Take telephone messages and provided feedback and answers to patient/pharmacy/physician calls. Professional attitudes sufficient to demonstrate honest, ethical…
$20 - $27 an hour
Quick Apply
13d
Clinical Research Assistant- Medical Oncology- ** Spanish Speaking**
Valkyrie Clinical Trials —Los Angeles, CA
Complete research test results; collates data; performs statistical analysis of lab results and maintain notes and log or computer database; performs basic…
$39,000 - $50,000 a year
Quick Apply
Clinical Research Coordinator
Quality Clincial Research —Omaha, NE
Work closely with the Principal Investigator and other team members to develop and implement research protocols. Clinical research: 1 year (Required).
$26 - $30 an hour
Quick Apply
8d
Sr. Clinical Research Associate
Avania —United States
Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the…
Estimated: $94.6K - $120K a year
Quick Apply
7d

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Clinical Research Coordinator, RN

Wichita Urology Group - Wichita, KS

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Job Details

Full-time From $50,000 a year 6 days ago

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Employee assistance program
Employee discount
Life insurance
Referral program

Qualifications

CCRC
Clinical research
RN License
Bachelor's degree
Clinical trials
FDA regulations

Full Job Description

Clinical Research Coordinator

Job Title: Clinical Research Coordinator - RN

Department: Clinical Research

Overtime Status: Exempt

Position reports to: Clinical Manager of Research

Location of position: Wichita, KS

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager and the Principal Investigator. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Responsibilities:

Coordinates with the Principal Investigator to help ensure that clinical research and related activities are performed in accordance with federal regulations and sponsor established policies and procedures.
Assists the PI 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. Documents date of training and signatures of study personnel trained on study specific training log.
Completes all protocol specific training (IATA, GCP, Protocol, EDC, IWRS, etc.)
Coordinates and facilitates monitoring and auditing visits. Notifies Clinical research manager and PI of external audits by FDA and sponsors.
Prepares documents for review by sponsors, monitors and regulatory authorities, as necessary
Participates in meetings with sponsors, monitors and regulatory authorities, as necessary.
Collaborates with PI and clinical research manager to respond to audit findings and implement approved recommendations.
Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.
Collaborates with the Clinical research manager and administrator to prepare a categorized budget and justification. Confirms accuracy and completeness of budgeted costs.
Assists the PI in study feasibility assessments and confidentiality agreements as requested.
Collects documents needed to initiate the study and submit to the sponsor (e.g., FDA Forms 1572, CVs, etc.).
Attends site selection meetings, site initiation visits, and investigator meetings as required or requested by the PI.
Reviews and comprehends the protocol.
Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Maintains study timelines by appropriately scheduling patients as outline in protocol
Collaborates with the PI to prepare IRB and any other regulatory submission documents to include protocol signature pages, protocol amendments, informed consent amendments, etc.
Works with the PI to develop and implement recruitment strategies in accordance with IRB requirements and approvals.
Conducts or participates in the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study.
Ensure written informed consent is obtained prior to participation in the study according to GCP and FDA guidelines.
Identify and promptly reports protocol deviations, AEs, and SAEs in accordance to protocol, IRB, and/or sponsor requirements
Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.
Prepares other study materials as requested by the PI. These study materials include, but are 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.
Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
Schedules and Interprets participant scans and procedures with outside contracted facilities.
Creates source documents and collects data as required by the protocol. Assures timely completion of Case Report Forms.
Dispenses IP and drug accountability (Accurately registering in IWRS and EDC receipt and dispensing or IP. Maintaining and accurately updating medication logs)
Maintains adequate inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and/or Wichita Urology Group Policy on Investigational Drug/Device Accountability.
Performs EKG, performs and interprets vital signs, obtains relevant laboratory specimens, and assists with physical exams, assessments, and procedures.
Completes study documentation and maintains study files in accordance with sponsor requirements (e.g., consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms).
Monitors and records temperature readings
Retains all study records in accordance with sponsor requirements and procedures.
Assists the Principal Investigator in submission of accurate and timely closeout documents to applicable federal agencies and sponsor in accordance with federal regulations and sponsoring agency policies and procedures.
Arranges secure storage of study documents that will be maintained according to university policy or for the contracted length of time, whichever is longer.

Required Qualifications:

Graduate of an accredited RN Program
Current Licensure by the Kansas State Board of Nursing
Maintenance of Continuing Education hours in accordance to Kansas State Board of Nursing requirements
Clinical Research coordinator experience
Certified Clinical Research Coordinator (CCRC) Designation Preferred
Strong interpersonal skills with ability to organize, multi-task and prioritize details
Ability to work well in team environment

Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Average, ordinary, visual acuity necessary to prepare or inspect documents or products, or operate machinery.
Prolonged periods of sitting, standing or walking may be required, should be able to transport approximately 0-25lbs of charts or files.
Occasional assistance in patient transfers of up to 50lbs.

Working Conditions:

While performing the duties of this job, the employee is frequently exposed to blood, body fluids, fumes, or airborne particles, and sharp objects potentially contaminated with blood borne pathogens or other infectious agents.

Wichita Urology Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, disability, gender identity or genetics. In addition to federal law requirements, Wichita Urology Group complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Wichita Urology Group expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Wichita Urology Group’s employees to perform their job duties may result in discipline up to and including discharge.

Job Type: Full-time

Pay: From $50,000.00 per year

Benefits:

401(k)
Dental insurance
Employee assistance program
Employee discount
Health insurance
Health savings account
Life insurance
Paid time off
Referral program

Schedule:

8 hour shift
Monday to Friday

Education:

Bachelor's (Preferred)

Experience:

Clinical Trials: 1 year (Preferred)
Clinical Research: 1 year (Preferred)

License/Certification:

Kansas State Board of Nursing License (Preferred)

Work Location: In person

Quick Apply

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