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 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
6d
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: $59.9K - $75.8K a year
12d
RN Clinical Research Coordinator - Full Time
Sanford Health —Fargo, ND
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
3d
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
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: $45.8K - $57.9K a year
Quick Apply
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
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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
Quick Apply
2h
Clinical Research Associate
Clinical Research Center of Florida —Miami Beach, FL
You will make a base salary of $50,000.00($25.00 per hour) and opportunity for bonuses based on performance.
$24 - $25 an hour
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2d
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 Trial Associate
Spectrum Staffing Services —Hopewell, NJ
Supports management and maintenance of filing systems for non-TMF documentation. The maintenance and management of assigned sites IRB initial submissions.
$70,000 a year
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
Quick Apply
2d
Research Associate
Diverge Translation Science Laboratory, LLC —Milwaukee, WI
Conduct a wide variety of protein analysis assays and data analysis independent of supervision in support of research and clinical trial related studies.
$52,000 - $63,000 a year
Quick Apply
4d
Senior Clinical Data Manager
Celldex Therapeutics, Inc. —New Haven, CT
Initiate CRF development for new clinical trials and protocol amendments; collaborate with internal team and responsible vendor on CRF development, database…
Estimated: $107K - $135K a year
Business Attraction and Investment Manager, CRA
City of Dania Beach —Dania Beach, FL
If the driver’s license is out of state, must be able to obtain a Florida driver’s license within thirty (30) days of the hire date. Apply now to join our team!
$66,181.32 - $102,580.95 a year
Clinical Research Associate
XBiotech USA, Inc —Austin, TX
RN or BA/BS degree in clinical, science or health related field. Contributes to site level recruitment strategy and contingency planning and implementation in…
Estimated: $69.1K - $87.5K a year
Quick Apply
4d
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
9d
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
Quick Apply
Clinical Research Assistant Coordinator
Connecticut Eye Consultants, P.C. —Danbury, CT
Position involves informing participants about clinical trials, conducting protocol visits, corresponding with study partners (sponsor, IRB, CRO, etc...),…
Estimated: $38.8K - $49.1K a year
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: $42.8K - $54.2K a year

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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 Associate

Clinical Research Coordinator I Registered Nurse

RN Clinical Research Coordinator - Full Time

Senior Clinical Research Coordinator

Clinical Research Coordinator (CRC)-FT

Clinical Research Assistant

Clinical Research Coordinator

Clinical Research Associate

Clinical Research Assistant/Medical Assistant

Clinical Trial Associate

Clinical Research Assistant

Research Associate

Senior Clinical Data Manager

Business Attraction and Investment Manager, CRA

Clinical Research Associate

Clinical Research Assistant/Medical Assistant

Clinical Research Coordinator

Clinical Research Assistant Coordinator

Clinical Manufacturing Associate I - Downstream

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