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
Delricht Research —New Orleans, LA
Clinical Research Coordinator’s Main Objective: *Overall, the Clinical Research Coordinator is responsible for providing quality, excellent patient care and a…
$48,000 - $55,000 a year
Quick Apply
14h
CRC / Clinical Research Coordinator - Cardiothoracic Surgery - Sponsored Research - Full Time - Days
ProMedica —Toledo, OH
RN with valid license given priority. Due to complex nature of tasks and extent of written and verbal communication, Science degree or degree in Health related…
Estimated: $55.9K - $70.8K a year
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…
Clinical Research Coordinator I
Nephrology Associates of Northern Illinois and Indiana (NANI) —Evergreen Park, IL
Bachelor’s Degree required in science, psychology or related field; or an additional 4 years relevant research experience in lieu of a degree.
Estimated: $52.4K - $66.4K a year
Quick Apply
Clinical Research Coordinator
Black Hills Regional Eye Institute —Rapid City, SD
A busy ophthalmic retinal practice is seeking an energetic individual with impeccable organizational skills to function as a full-time Clinical Research…
From $20 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: $62.2K - $78.8K a year
1d
Clinical Research Coordinator
Albuquerque Center for Rheumatology PC —Albuquerque, NM
*Technical (Medical) certification or 2 year science/healthcare degree preferred*. *Perform basic office duties such as filing, supply maintenance and…
$27.64 - $29.11 an hour
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In-house Clinical Research Associate
RHO —United States
Bachelors Degree in a life science, nursing or pharmacy field, along with at least 1 year of direct work experience managing essential documents within the CRO,…
$55,000 - $75,000 a year
1d
Sr. Clinical Research Associate
Huntington Study Group —United States
Bachelor’s degree, with major coursework in health, social science or biological science field or equivalent combination of education and experience.
$90,000 - $110,000 a year
Quick Apply
13d
Medical Research Associate
General Dynamics Information Technology —Agana Heights, GU
Provide operational support, to include analytical evaluations and prospective clinical evaluations, for diagnostic evaluations, clinical studies, and/or…
$44,625 - $60,375 a year
Clinical Research Associate 2, HSS
Yale University —New Haven, CT
All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug…
Estimated: $56.3K - $71.3K a year
1h
Clinical Research Associate (CRA) - Panama
KPS Life —United States
The CRA will provide support, training, and study procedure knowledge to the sites and study teams to ensure successful conduct and completion of the sponsor’s…
Estimated: $73.6K - $93.2K a year
4d
Clinical Research Assistant
SEC Clinical Research —Pensacola, FL
We require CMMA or LPN certification, and at least 2 yrs of clinical experience. This position also includes significant administrative responsibilities,…
$18 - $22 an hour
Quick Apply
Clinical Research Coordinator
ObjectiveHealth —Goodlettsville, TN
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: $49.3K - $62.5K a year
Quick Apply
9d
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: $44.3K - $56K a year
Clinical Research Associate
Baylor College of Medicine —United States
Master's degree in a related field. Conduct comprehensive literature searches in the areas of bioethics, social science, health policy, ELSI of genetics…
Estimated: $54.1K - $68.6K a year
1d
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: $53.9K - $68.2K a year
Global Clinical Trial Associate - Home-Based (US or Canada)
ICON —Remote
Ability to work well with cross-functional Study Team and investigational sites. The Clinical Trial Associate is responsible for providing support to Clinical…
Estimated: $61K - $77.2K a year
18h
Clinical Project Coordinator
Healthly Medical Group —Riverside, CA
Train providers on the board certification process for achieve board certification for lifestyle medicine through the American College of Lifestyle Medicine.
$55,000 a year
Quick Apply
1h

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Clinical Research Coordinator

CenExel Rocky Mountain Clinical Research - Englewood, CO

Quick Apply

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

CRC / Clinical Research Coordinator - Cardiothoracic Surgery - Sponsored Research - Full Time - Days

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

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator I Registered Nurse

Clinical Research Coordinator

In-house Clinical Research Associate

Sr. Clinical Research Associate

Medical Research Associate

Clinical Research Associate 2, HSS

Clinical Research Associate (CRA) - Panama

Clinical Research Assistant

Clinical Research Coordinator

Clinical Manufacturing Associate I - Downstream

Clinical Research Associate

Clinical Research Coordinator

Global Clinical Trial Associate - Home-Based (US or Canada)

Clinical Project Coordinator

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