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
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
8d
Clinical Site Manager (PT, OT, SLP)
Weisman Children's Rehabilitation Hospital —Marlton, NJ
Supports the implementation of approved site plans as outlined in the strategic plan and provides leadership through implementation.
Estimated: $72.9K - $92.4K a year
Quick Apply
5d
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
22h
Clinical Research Coordinator I
Texas Diabetes & Endocrinology, P.A. —Round Rock, TX
This position will require CCRC certification after meeting all Association of Clinical Research Professional (ACRP) CCRC hours.
Estimated: $56.7K - $71.8K a year
6d
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
22h
Clinical Research Site Manager
Texas Diabetes & Endocrinology, P.A. —Round Rock, TX
This person will answer staff questions regarding clinical trials and general office concerns. Provides a safe environment for patients, families, and clinical…
Estimated: $71K - $89.9K a year
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 Trial Associate - Home-Based (East Coast)
ICON —Remote
Experience with tools and systems for managing clinical trials such as Microsoft Project. Coordinate the filing of Trial Master File (TMF) documents in the …
Estimated: $63.6K - $80.6K a year
1d
Clinical Research Coordinator
Retina Consultants of Alabama —Birmingham, AL
\* Ensures each research team member has appropriate certification(s). \* Overall coordination of all functions for each clinical trial, including budget and…
$33 - $46 an hour
Quick Apply
Clinical Research Coordinator
Lexington Biomedical Research Institute —Lexington, KY
This position requires general office skills which include: answering phones, maintain study visit calendars, assisting staff, perform inventory of research…
$19,000 - $20,000 a year
Quick Apply
8h
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
Clinical Research Assistant
Clever Medical Research LLC —Miami, FL
General office tasks such as filing, copying, and scanning. The Research Assistant will ensure compliance with protocol and overall clinical objectives, and is…
Estimated: $30K - $35.2K a year
Quick Apply
6h
Clinical Research Coordinator
Sun Research Institute —San Antonio, TX
Ensure the filing and maintenance of all regulatory documents. Ensure patient’s referring physician receives notification of patient’s participation in studies…
Estimated: $43.8K - $55.4K a year
Quick Apply
Clinical Research Coordinator
One of a Kind Clinical Research Center CA LLC —Napa, CA
Data collection, entry, query resolution. We would like to add a full-time clinical research coordinator who can cooridnate current and future trial operations.
$23 - $25 an hour
Quick Apply
8d
Site Manager-Dorchester, MA
Care Access —Dorchester, MA
Act as a primary point of contact in the therapeutic field for Care Access Research. Ability and willingness to mentor and guide less experienced CRC as they…
Estimated: $84.2K - $107K a year
Quick Apply
Dermatology Clinical Research Assistant
Clear Dermatology & Aesthetics Center —Scottsdale, AZ
Assist research coordinator with patient study visits while ensuring compliance with clinical trial protocols. Schedule and confirm patient study appointments.
$16 - $20 an hour
Quick Apply
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 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

I want to receive the latest job alert for Clinical Research Associate

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

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

Clinical Site Manager (PT, OT, SLP)

Clinical Research Coordinator I Registered Nurse

Clinical Research Coordinator I

In-house Clinical Research Associate

Clinical Research Site Manager

Clinical Research Coordinator

Clinical Trial Associate - Home-Based (East Coast)

Clinical Research Coordinator

Clinical Research Coordinator

Sr. Clinical Research Associate

Clinical Research Assistant

Clinical Research Coordinator

Clinical Research Coordinator

Site Manager-Dorchester, MA

Dermatology Clinical Research Assistant

Clinical Manufacturing Associate I - Downstream

Clinical Research Associate

Clinical Research Assistant

Job Seeker Tools

Employer Tools

Browse

Stay Connected