20 Best Clinical Research Associate jobs (Hiring Now!)

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
Quick Apply
Clinical Management Coordinator
Charleston Area Medical Center (CAMC) —Charleston, WV
Develop and implement testing methods and techniques for psychological assessment. Provide psychological assessment, treatment, and education regarding the…
Estimated: $77.9K - $98.6K a year
Quick Apply
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
19h
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
8h
GME Research Coordinator
Northeast Georgia Health System —Gainesville, GA
Minimum Experience: Minimum of five years experience in healthcare research, public health research and/or academic science or PhD in related area, and evidence…
Estimated: $80.8K - $102K a year
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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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…
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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3d
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
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11d
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
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
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 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
7d
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…
Quick Apply
11d
Clinical Research Coordinator
Alliance for Multispecialty Research, LLC —Norman, OK
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
$24 - $26 an hour
Quick Apply
5d
Clinical Trials Associate US REMOTE
Worldwide Clinical Trials —Oregon
Assist with the tracking and maintenance of project related information, including site medical question and answer log.
Estimated: $49.9K - $63.2K a year
Quick Apply
4d
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: $96.9K - $123K a year
Quick Apply
13d
Clinical Research Coordinator
Delricht Research —Tulsa, OK
Accurately and efficiently conduct patient charting and review your own work for accuracy and quality. *Required:* Experience with high touch documentation or…
$48,000 - $55,000 a year
Quick Apply
6d
Clinical Research Assistant
Diablo Clinical Research, Inc. —Walnut Creek, CA
The first four weeks of the program will be focused on the basic concepts of clinical research and their implementation at the clinical site level and learning…
$20 an hour
Quick Apply
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

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Clinical Research Coordinator

CenExel iResearch - Decatur, GA

Quick Apply

Job Details

Full-time Estimated: $45.8K - $58K a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance
Life insurance
Referral program

Qualifications

Clinical research
Patient monitoring
Bachelor's degree
Clinical trials
1 year
Care plans
Medical terminology

Full Job Description

ABOUT US

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

JOB SUMMARY

Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. This is a Full Time opportunity, Monday-Friday from 8am-5pm.

DUTIES AND RESPONSIBILITIES DESCRIPTION

Coordinating all aspects of patient involvement from study initiation until study completion;

Study start-up:

o assist in the creation of thorough and accurate source documents;

o Work collaboratively with other internal departments, sponsors and investigators to ensure protocols are understood and assist in the trainings of staff members

o Participate in IMs and SIVs; communicating with sponsors and representatives

o Ensure site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)

o Screening participants for actively enrolling studies

o Assist in reviewing all participant history from Pre-Enrollment and Enrollment departments confirming information with potential participant and study physician

o Educating potential participants and caregivers on protocol specific details and expectations;

o Working with the physician to address all questions and concerns related to the trial and informed consent process;

o Maintaining thorough knowledge of study specific inclusion/exclusion criteria

o Coordinating scheduled visits and adhering to protocol visit windows and timelines

o Perform or follow up on safety and efficacy assessments per protocol

 vital signs, EKGs, blood draws and other assessments as assigned

o Collaborating with the research pharmacist to perform drug accountability and compliance at each visit and educating subject on proper dosing regimen

o Accurate and timely completion of source documents recording subject’s participation in study

o Communicate closely with all departments to ensure study visits are coordinated in compliance with protocol and GCP guidelines

o Assist investigators in collection of information from study subjects regarding AEs, concomitant medications and other changes throughout participation

o Responsible for subject scheduling, in coordination with Recruiting

o Responsible for timely data entry and query resolution

o Timely reporting of study events (SAEs, protocol deviations, etc) to appropriate departments and other outside agencies (Sponsors, CRO’s, etc.)

o Following subjects through study completion and creating follow-up care plan with physician, study subject and primary care provider;

Ensuring preparation for and facilitating of all study monitoring visits and following up promptly with monitor follow-up letters

Prompt and professional communication with sponsors, representatives and other study related parties

Maintaining professional and appropriate interactions with study subjects, caregivers, sponsors and all other study related personnel, and staff members

Keeping management informed of study status and any study-related issues Assumes other duties and responsibilities as assigned.

The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

EDUCATION/EXPERIENCE/SKILLS

Bachelor's Degree or equivalent experience in Clinical Research or related field. Demonstrated expertise in: o knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials

o providing strong leadership and mentorship to others

o developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level

o crisis management and problem solving; ability to react calmly and effectively in emergent situations o working independently as well as functioning as part of a team

o communicating clearly both written and verbally Highly proficient in:

o In the use of technology required for the completion of study visits and study conduct o completing paperwork with precision, accuracy, and attention to detail

o meeting timelines and attention to detail

o prioritizing daily tasks with minimal guidance

o using medical equipment and instruments to administer study subject care

o medical terminology

Must be able to effectively communicate verbally and in writing.

WORKING CONDITIONS

Indoor, office environment. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Job Type: Full-time

Benefits:

401(k)
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Referral program
Vision insurance

Schedule:

8 hour shift
Monday to Friday

Education:

Bachelor's (Preferred)

Experience:

Clinical research: 1 year (Required)

Ability to Relocate:

Decatur, GA 30030: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Clinical Research Associate jobs

Clinical Research Coordinator

Clinical Management Coordinator

RN Clinical Research Coordinator - Phase 1 Oncology - Full Time

Oncology Clinical Research Associate - IQVIA Biotech

GME Research Coordinator

Experienced Clinical Research Coordinator

Assistant Director – Pre-Award Clinical Trials (Vanderbilt Ingram Cancer Center)

Lead Clinical Research Coordinator

Clinical Research Coordinator PRN

Sr. Clinical Research Associate

Clinical Research Coordinator (local recruits only)

Clinical Research Assistant

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Trials Associate US REMOTE

Senior Clinical Research Associate

Clinical Research Coordinator

Clinical Research Assistant

Clinical Research Assistant- Medical Oncology- Spanish Speaking

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