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Clinical research assistant skills for your resume and career

15 clinical research assistant skills for your resume and career
1. Patients
- Conducted follow-up visits on all clinical trial participants, monitoring and data recording of patients information into defined databases.
- Developed protocol-specific documents for ease of tracking patients and regulatory documents, to ensure regulatory and protocol compliance.
2. Informed Consent
- Recruited patients for Phase IV clinical trials by determining eligibility, inclusion/exclusion criteria, taking informed consent and approval.
- Screened subjects for eligibility in accordance with study protocol, participated in informed consent process, maintained study files.
3. Data Collection
Data collection means to analyze and collect all the necessary information. It helps in carrying out research and in storing important and necessary information. The most important goal of data collection is to gather the information that is rich and accurate for statistical analysis.
- Tracked/coordinated/facilitated follow-up visits & data collection.
- Presented necessary clinical updates to Principal Investigators and research coordinators in order to identify any data collection or recruitment procedure gaps.
4. Data Entry
Data entry means entering data into a company's system with the help of a keyboard. A person responsible for entering data may also be asked to verify the authenticity of the data being entered. A person doing data entry must pay great attention to tiny details.
- Trained departmental supervisors and employees on implementation techniques involving personnel training and data entry guidelines vital to computer conversion target dates.
- Provided precise documentation of study-related issues and ensured proper data entry into laboratory and research databases.
5. IRB
An institutional review board (IRB), is a form of committee that applies research ethics by vetting research procedures to ensure they are ethical. In order to decide whether or not research can be undertaken, they often perform a kind of risk-benefit analysis. The IRB's function is to ensure that adequate safeguards are in place to protect the interests and health of humans who are participants of a research sample.
- Obtained clinical information using IRB protocol standards and consulted with the principal investigator regarding the study.
- Submitted regulatory documents to internal regulatory affairs including IRB information and 1572 forms.
6. Patient Care
Patient care entails the diagnosis, recovery, and control of sickness as well as the maintenance of physical and emotional well-being through the use of healthcare providers' services. Patient care is described as services provided to patients by health practitioners or non-professionals under guidance.
- Gathered information and proper history of patients; conduct physical examination and learned proper patient care.
- Assisted with in-patient care including taking medical history, performing problem-focused and full examinations.
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- Assisted with the administration of clinical research projects, recruiting investigators, collecting investigator documentation and site management.
- Collected and entered data for existing research projects and assisted in the implementation of future opportunities.
8. Clinical Trials
- Supported the Directors of Respiratory & Clinical Trial Management with PowerPoint presentations used at Speakers Bureaus, symposiums and medical conventions.
- Provide excellent management, planning, and supervision skills to administer up to 10 cardiovascular and diabetic clinical trials simultaneously.
9. Research Data
- Managed MFT clinic administration conducting in-take assessments, observing and coding therapy sessions and logging research data.
- Gathered research data and participated in conference calls with University of Virginia psychological department staff
10. Data Management
The administrative process that involves collecting and keeping the data safely and cost-effectively is called data management. Data management is a growing field as companies rely on it to store their intangible assets securely to create value. Efficient data management helps a company use the data to make better business decisions.
- Analyzed imaging and spectroscopy data and performed data management using different computer platforms and statistical packages including SPSS and SAS.
- Worked with outside diagnostic team in data management and bi-annual information auditing process as dictated by study protocols.
11. Clinical Research Studies
- Monitored anti-microbial clinical research studies, carried out site visits verifying data recorded for patients and recorded outcomes.
- Conducted clinical research studies, reviewed study files, tracked and managed case report forms and responded to queries.
12. Excellent Organizational
- Demonstrated excellent organizational skills by tracking all project activities in databases to accurately report clinical trial progress.
- Provided excellent organizational, communication, and planning skills in responding to requested information.
13. Coordinators
- Assisted oncology clinical research coordinators by copying medical records of research subjects per institutional protocols.
- Meet with Principal Investigators and Study Coordinators to ensure adherence to Clinical Trial Protocol.
14. Institutional Review
- Reviewed regulatory documents received from sites prior to submission to Institutional Review Boards.
- Process all Institutional Review Board documentation received upon arrival.
15. HIPAA
- Monitored compliance of research protocols across departments; ensured patient confidentiality under HIPAA regulations.
- Protected customer and patient confidentiality by following all HIPAA standards.
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What skills help Clinical Research Assistants find jobs?
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What skills stand out on clinical research assistant resumes?
Associate Professor of Arabic, The University of New Mexico
What technical skills for a clinical research assistant stand out to employers?
Professor, University of Wisconsin – La Crosse
What soft skills should all clinical research assistants possess?
Research Professor Financial Engineering, Director Hanlon Laboratories, Director Financial Analytics program, Stevens Institute of Technology
What hard/technical skills are most important for clinical research assistants?
Harriet Phinney Ph.D.
Associate Professor, Seattle University
List of clinical research assistant skills to add to your resume

The most important skills for a clinical research assistant resume and required skills for a clinical research assistant to have include:
- Patients
- Informed Consent
- Data Collection
- Data Entry
- IRB
- Patient Care
- Research Projects
- Clinical Trials
- Research Data
- Data Management
- Clinical Research Studies
- Excellent Organizational
- Coordinators
- Institutional Review
- HIPAA
- Phlebotomy
- Excellent Interpersonal
- GCP
- Vital Signs
- Literature Searches
- FDA
- Human Subjects
- Data Analysis
- Patient Data
- Consent Forms
- Oncology
- EKG
- Clinical Data
- Study Procedures
- Phone Calls
- SPSS
- CRA
- Study Subjects
- Research Assistants
- Literature Reviews
- NIH
- MRI
- SAS
- Regulatory Binders
- ICH
- EMR
- Consent Process
- IV
- Patient Recruitment
- Patient Charts
- Clinical Practice
- Blood Draws
- Medical History
- Research Subjects
Updated January 8, 2025