20 Best Clinical Research Associate jobs (Hiring Now!)

Clinical Research Coordinator
CenExel Rocky Mountain Clinical Research —Englewood, CO
CCRC certification not required, but preferred. O Responsible for timely data entry and query resolution. Knowledge of all components of the research process as…
$29 - $32 an hour
Quick Apply
Clinical Research Coordinator I Registered Nurse
Novant Health —Charlotte, NC
Licensure/Certification: Current RN licensure in appropriate state, required. Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects…
Estimated: $57K - $72.2K a year
7d
Clinical Research Coordinator (CRC)-FT
Evolution Research Group —Columbus, OH
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Estimated: $49.3K - $62.4K a year
Quick Apply
Clinical Research Associate
ProTrials Research, Inc. —United States
A valid driver's license with access to a car with up-to-date car insurance. Bachelor and/or advanced degree in biological sciences or related field, or…
$85,000 - $130,000 a year
1d
Senior Clinical Research Coordinator
Evolution Research Group —Staten Island, NY
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
$30 - $38 an hour
Quick Apply
13d
Clinical Research Assistant
Alliance for Multispecialty Research LLC —Knoxville, TN
Assist in general office workflow which includes telephone answering. Answering and triage of research office calls. Filing and pulling study records.
$20 - $24 an hour
Quick Apply
Clinical Research Coordinator
Alliance for Multispeciality Research —New Orleans, LA
Attach original document to certified copy before filing in the patient’s chart. Advise Investigator, Sub-Investigator and staff on protocols, procedures…
$24 - $27 an hour
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12d
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
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Clinical Manufacturing Associate I - Downstream
Rocket Pharmaceuticals —Cranbury, NJ
Additional responsibilities include set-up, operation, and cleaning of equipment, equipment, and process monitoring and troubleshooting, receiving materials and…
Estimated: $45.3K - $57.4K a year
Clinical Project Associate (REMOTE)
Fresenius Medical Care —Meriden, CT
Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
Estimated: $77.7K - $98.4K a year
1d
Clinical Site Manager
Urology of Virginia PLLC —Suffolk, VA
Credentialed as a Medical Assistant or other nursing related field of study. Minimum of 5 years’ clinical experience.
Estimated: $94.2K - $119K a year
Quick Apply
Research Administrative Assistant
Colorado Urology Associates —Lakewood, CO
A High School Diploma is required; an associate's degree or equivalent experience in a relevant field is preferred. Schedule and manage research appointments.
$20 - $23 an hour
Quick Apply
1d
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
1d
Clinical Research Associate 1
Connecticut Children's Medical Center —Farmington, CT
Bachelor’s or Master’s degree in a health care related field; degrees in other areas may be substituted on a case-by-case basis.
Estimated: $64.4K - $81.6K a year
1d
Research Associate - Orthopedic Research - CORIT Lab
GuideWell —Houston, TX
May recruit study participants or field interviewers. Bachelor’s degree in a related field with three (3) years of related research experience including…
Estimated: $50.2K - $63.6K 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
4d
Clinical Trials Vendor Specialist
CPC Clinical Research —Aurora, CO
CPC is an academically led clinical research organization that offers full service clinical trial design, oversight, and management with rapid access to Key…
$75,000 - $90,000 a year
Quick Apply
13h
Clinical Research Assistant/Medical Assistant
Alliance for Multispeciality Research, LLC —Kansas City, MO
Assist in general office workflow which includes telephone answering. O Answering and triage of research office calls. O Filing and pulling study records.
$21 - $23 an hour
Quick Apply
Clinical Research Associate
Kerecis —Minneapolis, MN
Support data analysis projects through data entry, data cleaning, data validation and data analysis. Knowledge of laboratory certification processes and…
Estimated: $70.1K - $88.7K a year
1d
Clinical Research Coordinator
Healthcare Hiring Firm —Fayetteville, NC
Identifies and reports issues that may affect the accuracy and quality of study design and implementation to meet study aims.
$75,000 - $110,000 a year
Quick Apply
5h

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Clinical Research Coordinator

CenExel Rocky Mountain Clinical Research - Englewood, CO

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Job Details

Full-time $29 - $32 an hour

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Employee discount
Flexible schedule
Life insurance

Qualifications

Microsoft Word
CCRC
Microsoft Excel
Clinical research
Phlebotomy
Clinical trials
Good Clinical Practice
Computer skills
Neurology
1 year
Care plans

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.

Essential Responsibilities and Duties:

· 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.)

· 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

· 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:

At least 1 years of experience working as a Clinical Research Coordinator.
CCRC certification not required, but preferred
Experience in neurology not required, but preferred
Knowledge of “good clinical practices” for clinical research as defined by the Code of Federal Regulations (CFR).
Demonstrate organizational skills to efficiently and effectively manage multiple clinical trials while providing accurate information in a timely manner.
Communicate and work effectively with a diverse team of professionals
Phlebotomy and ECGs experience not required, but preferred
Knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.
Demonstrated interpersonal skills to work with physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
Must be self-directed and be able to manage multiple projects and responsibilities.
Computer skills using PC platform computers with proficiency in Excel and Word to enter data and generate correspondence accurately and experience with various EDC platforms
Experience with IRB portals, such as WIRB and Advarra preferred
A critical thinker with strong attention to detail and superb problem-solving abilities.

Compensation: $28-32/h.

Application window will close on June 25th, 2024.

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

Pay: $29.00 - $32.00 per hour

Benefits:

401(k) matching
Dental insurance
Employee discount
Flexible schedule
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Experience:

Clinical research: 1 year (Required)
randomizing patients: 1 year (Required)
conducting patients visits: 1 year (Required)

Ability to Commute:

Englewood, CO 80113 (Required)

Work Location: In person

Quick Apply

Clinical Research Associate jobs

Clinical Research Coordinator

Clinical Research Coordinator I Registered Nurse

Clinical Research Coordinator (CRC)-FT

Clinical Research Associate

Senior Clinical Research Coordinator

Clinical Research Assistant

Clinical Research Coordinator

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

Clinical Manufacturing Associate I - Downstream

Clinical Project Associate (REMOTE)

Clinical Site Manager

Research Administrative Assistant

Clinical Research Coordinator

Clinical Research Associate 1

Research Associate - Orthopedic Research - CORIT Lab

Clinical Research Assistant/Medical Assistant

Clinical Trials Vendor Specialist

Clinical Research Assistant/Medical Assistant

Clinical Research Associate

Clinical Research Coordinator

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