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Clinical researcher skills for your resume and career
15 clinical researcher skills for your resume and career
1. Patients
- Educated eligible patients about our research study, and explained potential benefits of study participation.
- Interacted with and assessed patients to determine effectiveness of medicine.
2. Informed Consent
- Obtain informed consent, gather clinical and research data.
- Organized all forms, administered Informed Consents, administered Investigational Product.
3. 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.
- Served as the IRB liaison for the Division of Urology.
- Gathered and prepared documents for IRB submission.
4. Clinical Trials
- Supported clinical trial implementation through technological support and creating care team resources.
- Improved efficiency and ensured compliance of clinical trial registration across the different global platforms in accordance with WHO and ICJME requirements.
5. 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.
- Managed relationships with consultants to provide adequate support and services for data collection and analysis.
- Collaborated with team to complete research tasks and data collection efficiently and effectively.
6. FDA
The Food and Drug Administration (FDA) is a division of the US Department of Health and Human Services that regulates the production and sale of food, pharmaceutical products, medical equipment, and other consumer goods, as well as veterinary medicine. The FDA is now in charge of overseeing the manufacture of products like vaccines, allergy treatments, and beauty products.
- Prepared for and guided coordinators, medical directors, and investigators during FDA audits and sponsor initiated quality assurance audits.
- Coordinated pharmaceutical hypertension research protocols within FDA guidelines; maintained critical documents; prepared strategies for patient recruitment and retention.
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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.
- Created requirements for computer programs for data management and/or analysis for individual projects/trials.
- Transformed clinical trial data and loaded into Clinical Data Management System.
8. 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.
- Created various forms of databases including forms and reports for ease of data entry and information retrieval Certifications and Memberships
- Trained departmental supervisors and employees on implementation techniques involving personnel training and data entry guidelines vital to computer conversion target dates.
9. HIPAA
- Prepared and submitted all regulatory documentation in compliance with Institutional Review Board and HIPAA guidelines.
- Study regulatory document (ICF, HIPAA) development/writing/editing/revising/resolution/implementation/correspondence for the IRB process.
10. Clinical Research Studies
- Worked directly with industry sponsors in initiating and conducting clinical research studies as coordinator and sub-investigator.
- Coordinated clinical research studies involving cognitively healthy older adults, older adults with cancer and subjects with Alzheimer's disease.
11. Data Queries
- Reviewed, clarified, and resolved data queries.
- Respond in a timely manner to data queries requested by investigators and regulatory agencies.
12. Consent Forms
Consent forms refer to something that a person signs or attests to in order to agree for something that involves them to happen. They are used in various fields and applications. It is a legal document that can have repercussions if forged or denied later. In medical terms, it is the informed consent of the patient agreeing to the medical procedure they are about to undergo in a sound state of mind.
- Entered patient data per visit requirements and maintained proper consent forms necessary for patient participation in studies.
- Assist PI in written modifications of investigator initiated protocols and consent forms.
13. NIH
NIH stands for the National Institutes of Health. This organization oversees a series of research institutions, each focused on a different area of study involving anatomical systems or diseases. As the organization is affiliated with the government, a great deal of the funding institutions receive come from Congress.
- Prepared drafts and manuscripts for NIH grants and assisted principal investigators in finalizing submissions.
- Perform research protocols based on NIH Guidelines, particularly the study on HIV transmission and educated clients on their disease process
14. Institutional Review
- Tracked adherence to Institutional Review Board protocols.
- Assist investigators with correspondence involving the Institutional Review Board, including preparation of New and renewal applications, and amendments.
15. Epic
Epic is a private healthcare company which developed and continues to provide a software intended for healthcare professionals and the organization and management of medical records. It is by far one of the largest in its field, with over 50% of patients having a medical record present in their system. Patients, as well as clinics and various medical professionals and facilities are all able to use this system to keep medical history and information safe and easy to reach, alter, and share with the necessary people.
- Looked up patient information utilizing electronic medical records such as Epic.
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What skills help Clinical Researchers find jobs?
Tell us what job you are looking for, we’ll show you what skills employers want.
What clinical researcher skills would you recommend for someone trying to advance their career?
Dr. Judson Jeffries
Professor, Ohio State University
What technical skills for a clinical researcher stand out to employers?
Assistant Professor of Spanish, Foreign Languages Division Coordinator, Faculty Affiliate, Center for Critical Race & Ethnic Studies, Florida Gulf Coast University
What soft skills should all clinical researchers 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 researchers?
Dr. Sharon Locke Ph.D.
Director, Center for STEM Research, Education, and Outreach, Professor, Department of Environmental Sciences, ISSP Sustainability Excellence Associate, Southern Illinois University Edwardsville
-How to design a research study/experimental design.
-GIS skills
-Environmental statistics skills
-Knowledge of lab and field safety protocols
-Something that helps an applicant to stand out, such as drone pilot certification.
List of clinical researcher skills to add to your resume

The most important skills for a clinical researcher resume and required skills for a clinical researcher to have include:
- Patients
- Informed Consent
- IRB
- Clinical Trials
- Data Collection
- FDA
- Data Management
- Data Entry
- HIPAA
- Clinical Research Studies
- Data Queries
- Consent Forms
- NIH
- Institutional Review
- Epic
- Data Analysis
- Patient Data
- Consent Process
- Research Projects
- Infectious Disease
- Clinical Data
- Federal Regulations
- EMR
- MRI
- CRO
- Patient Recruitment
- Statistical Analysis
- Clinical Trial Management
- Vital Signs
- IND
- Rehabilitation
- Research Organization
- Blood Samples
- Biomarkers
- EDC
- CRF
- CRA
- Literature Reviews
- HIV
- Blood Pressure
- Query Resolution
- Diabetes
- Immunization
- Phase II
Updated January 8, 2025