Research Assistant
Clinical Research Assistant
Clinical research assistants help make sure that medical and drug research meets high standards. They do this by making sure that the data collected is accurate and by creating reports. Clinical research assistant certification demonstrates a commitment to professionalism and ethical compliance.

Research Assistant
A research assistant is a professional who works with scientists, engineers, and other professionals to perform research duties. They may be responsible for data collection, laboratory work, managing research projects and coordinating clinical trials.
Clinical research assistant
A research assistant assists with literature reviews, designing experiments and data collection & analysis tasks, as well as administrative duties such as editing manuscripts & presentations and preparing grant applications.A clinical research assistant does tasks such as collecting patient data, scheduling appointments, preparing consent forms, and responding to queries from patients or study participants.
Clinical trial assistants help clinical research coordinators with conducting clinical trials. This includes uploading and downloading study documents, scheduling appointments, collecting data, updating patient information in the system, managing databases, preparing for patient visits, filing reports, tracking regulatory documents and coordinating communication between sponsors and sites.
When you are making a research assistant resume, it is important to show that you have the right certification, have done coursework related to the job, have done things that show you are good at science, have worked on research projects before, and know what protocols and industry regulations to follow. You must always include a good cover letter for a research assistant position.
Clinical Trial Assistant Certification
Clinical Research Assistant Course Syllabus
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2
Fundamentals of Clinical Research
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An Introduction to Clinical Research
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An Overview of ICH GCP
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Code of Federal Regulations
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CFR 21 Part 11
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3
Clinical Trial Roles and Responsibilities
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Sponsor/CRO Responsibilities
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13 Principles, IRB, & Investigator Roles
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4
Informed Consent & Patient Safety
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5
Adverse Event Reporting & Responsibilities
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Reporting Responsibilities of the Investigators
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Adverse Events
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6
Ethical Research in Vulnerable Populations
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Ethics of Research Involving Children
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Ethics of Research Involving Mentally Incapacitated
FREE PREVIEW -
Ethics of Research Involving Pregnant Women and Fetuses
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Ethics of Research Involving Prisoners
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7
Trial Management, Data Handling, and Record Retention
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Trial Management – Data Handling and Record Retention
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a) Common Terminology Used In Clinical Research
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b) Commonly Used Abbreviations and Terms in Clinical Research
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8
Clinical Trials - Advanced Review
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Advanced Designs of Clinical Trials
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Advanced Review of Phases of Clinical Trials (Preclinical & Phase 0-4)
FREE PREVIEW
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9
Subject Recruitment, Retention, and Compliance
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Patient Recruitment in Clinical Trials
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Patient Engagement and Retention in Clinical Trials
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Patient Adherence and Compliance in Clinical Trials
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10
Misconduct and Fraud
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Scientific Misconduct and Fraud
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Detecting Falsification
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11
Clinical Trial Assistant Certification Exam
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ICH GCP Clinical Trials Assistant Exam (30 Questions)
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Research Assistant Salary
The average salary for a research assistant job is $47,000 per year. This number changes depending on where the job is and other things. Usually, clinical research assistants who work in the medical field make more money than people in other areas.
Research Assistant Jobs
Your job will be to do things like make appointments and order supplies. You will also help with our clinical research projects by doing things like entering data into databases, collecting and analyzing data, and making sure that project documentation is accurate. You will help make sure we comply with all applicable regulatory standards.
Being able to manage multiple projects at the same time efficiently, with a focus on coordinating sample collection and data analysis for clinical research studies. Having a track record of success in developing and carrying out protocols for analyzing patient data, including collecting, entering, and cleaning of data using standard software programs.
I know how to do research projects and can help any research team. I am good at doing administrative tasks like keeping records, helping with communications, taking notes during meetings/interviews, preparing presentations/reports, and making sure that the research team is following ethical standards & protocols.
Clinical Research Assistant
The Clinical Research Assistant Certification from CCRPS offers affordable comprehensive instruction and content that is accessible 24/7 through any device. This allows students to work at their own pace without strict deadlines. With full accreditation from the ACCRE, AMA, ACPE, ANCC, and IPCE organizations, CCRPS's certification is highly esteemed and respected in the clinical research industry.