Clinical Research Associate

Clinical Research Associate Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Clinical Research Associate job postings. In other words, these are the most sought after skills by recruiters and hiring managers. Go to Sample Templates ↓ below to see how to include them on your resume.

Remember that every job is different. Instead of including all keywords on your resume, identify those that are most relevant to the job you're applying to. Use the free Targeted Resume tool to help with this.

Choose a category
  • Good Clinical Practice (GCP)
  • Clinical Monitoring
  • Clinical Trial Management System (CTMS)
  • Electronic Data Capture (EDC)
  • Clinical Trials
  • Clinical Research
  • Protocol
  •  Find out what your resume's missing
  • Clinical Development
  • CRO Management
  • Oncology
  • Clinical Research Associates
  • Clinical Data Management
  • Standard Operating Procedure (SOP)
  • Therapeutic Areas
  • Clinical Operations
  • Oncology Clinical Research
  • Regulatory Submissions
  • U.S. Food and Drug Administration (FDA)
  • Clinical Site Monitoring
  • Biotechnology

  •   Show full list

Resume Skills: Regulations

  • GCP
  • ICH Guidelines
  • FDA
  • EMA
  • Good Clinical Practice (GCP)
  • FDA Regulations
  • Health Insurance Portability and Accountability Act (HIPAA)
  • FDA regulations
  • ICH guidelines
  • Code of Federal Regulations Title 21
  • SOP
  •  Match your resume to these skills

Resume Skills: Languages

Resume Skills: Software

  • Oracle Clinical
  • Medidata Rave
  • Microsoft Office Suite (Excel, PowerPoint, Word)
  • MS Office Suite
  • ClinCapture
  • OpenClinica
  • CTMS
  • SPSS
  • SAS
  • Clinical Trial Management System (CTMS)
  • EDC Systems
  • Clinical Conductor
  • Inform
  • Electronic Data Capture (EDC) Systems
  • Statistical Software (SAS, SPSS)
  • Citrix
  • R
  • Stata
  • Prism
  • Seagull
  • Microsoft Office
  • Clinical Data Management System (CDMS)
  • Medidata
  • REDCap
  • Clinical Data Management
  • Biostatistics
  •  Match your resume to these skills

Resume Skills: Technical

  • Clinical Data Management System (CDMS)
  • Quantum
  • SAS
  • Oracle Clinical
  • Medrio
  • Clinical Trial Data Reporting
  • MS Office
  • Electronic Health Records (EHR)
  • Python for Data Analysis
  • Clinical Data Management Systems (CDMS)
  •  Match your resume to these skills

Resume Skills: Regulatory Knowledge

Resume Skills: Project Management

  • Stakeholder Management
  • Risk Management
  • Agile and Scrum methodologies
  • Risk Assessment
  • Budgeting
  • Contract Negotiation
  • Time Management
  • Decision Making
  •  Match your resume to these skills

Resume Skills: Clinical Research

  • Clinical Trial Design
  • Clinical Data Management
  • Regulations Compliance
  • Scientific Writing
  • Designing and Conducting Clinical Trials
  • Regulatory Compliance
  • Patient Recruitment
  • Data Analysis
  • Site Monitoring
  • Report Writing
  • Clinical Trials Management
  • Drug Development Process
  • Data Collection and Analysis
  • Protocol Development
  • Data Management
  • Clinical Monitoring
  • Adverse Event Reporting
  • Regulatory Submissions
  • Clinical Trial Protocols
  • IRB Submissions
  • Clinical Trial Monitoring
  • Ethics in Clinical Research
  • Clinical Trial Designs
  • Data Collection & Analysis
  • Biostatistics
  • Clinical Trial Management
  • Phase I-IV Trials
  • Clinical Study Design
  • Good Clinical Practice (GCP)
  • Protocol development
  • Clinical monitoring
  • Regulatory compliance
  • Data collection and analysis
  • Quality Assurance
  • Risk Management
  •  Match your resume to these skills

Resume Skills: Biomedical Techniques

Resume Skills: Technologies and Tools

Resume Skills: Data Analysis & Statistics

Resume Skills: Medical

Resume Skills: Communication & Documentation

Resume Skills: Regulatory & Quality Assurance

Resume Skills: Regulation and Compliance

  Does your resume contain all the right skills? Paste in your resume in the AI Resume Scan ↓ section below and get an instant score.

Compare Your Resume To These Clinical Research Associate Skills (ATS Scan)

Paste your resume below and our AI will identify which keywords are missing from your resume from the list above (and what you need to include). Including the right keywords will help you get past Applicant Tracking Systems (i.e. resume screeners) which may scan your resume for keywords to see if you're a match for the job.

Sample Clinical Research Associate Resume Examples: How To Include These Skills

Add keywords directly into your resume's work experiences, education or Skills section, like we've shown in the examples below. Use the examples below as inspiration.

Select a free resume example
Your Name
Clinical Research Associate
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded January 2020 - Present
Senior Clinical Research Associate
Developed 4 clinical trial protocols, adhering strictly to Good Clinical Practice (GCP) guidelines, resulting in 100% approval by the FDA.
Managed a team of Clinical Research Associates, resulting in an improved completion of clinical trial objectives by 25%.
Utilized Clinical Trial Management System (CTMS) to monitor 10+ clinical trials, reducing data inconsistencies by 18%.
Applied Electronic Data Capture (EDC) in data management, leading to a 30% improvement in data accuracy and efficiency.
Oversaw oncology clinical research which led to the successful submission of 2 Investigational New Drug (IND) applications.
AstraZeneca May 2016 - January 2020
Clinical Research Associate
Coordinated with 5+ sites for clinical monitoring, ensuring compliance with study protocols and improving data quality.
Carried out regulatory submissions for 10+ clinical trials ahead of schedule, increasing process efficiency by 15%.
Implemented standard operating procedures (SOPs) for clinical site monitoring, reducing protocol deviations by 20%.
Biogen April 2015 - April 2016
Junior Clinical Research Associate
Enhanced data management by adopting Clinical Data Management Systems (CDMS), improving data validation by 10%.
Assisted in managing Clinical Trial Protocols for two major studies.
Participated in site selection, leading to the onboarding of 8 highly compliant clinical trial sites.
Resume Worded University January 2015
Master of Science in Clinical Research
Focus on Biostatistics and Epidemiology
Resume Worded Academic Center May 2010
Bachelor of Science in Life Sciences
Emphasis on Human Anatomy and Biochemistry
Dean's List 2008, 2009 (Top 10%)
Technical Skills: Clinical Data Management System (CDMS), Quantum, SAS, Oracle Clinical, Medrio, Clinical Trial Data Reporting
Regulatory Knowledge: ICH-GCP guidelines, FDA regulations, Clinical research ethics
Project Management: Stakeholder Management, Risk Management, Agile and Scrum methodologies
Languages: English (Native), Spanish (Fluent), German (Basic)
Certifications: Clinical Research Certification (CRC) - Association of Clinical Research Professionals, Certified Clinical Research Associate (CCRA) - The Society of Clinical Research Associates
Leadership & Volunteering: Co-Founder and Chair, Global Clinical Research Community, Volunteer at Health Workers Unite NGO
Projects: Led end-to-end execution of a phase II trial in oncology, resulting in publication in The Lancet
Awards: Rising Star in Clinical Research - Association of Clinical Research Professionals, Excellence in Clinical Research - Biogen
Your Name
Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded February 2021 - Present
Clinical Research Manager
Supervised a team of 10 Clinical Research Coordinators, boosting team productivity by 30%.
Processed data from various therapeutic areas, resulting in 10 new breakthrough findings.
Optimized Clinical Trial Management System (CTMS) usage, leading to 15% enhanced team efficiency.
Orchestrated oncology clinical research, resulting in 5 new drug development opportunities.
Managed the preparation of 6 Investigational Medicinal Product Dossier (IMPD) submissions to U.S. Food and Drug Administration (FDA). July 2018 - January 2021
Clinical Research Coordinator
Managed data from Electronic Data Capture (EDC) for 5 clinical trials, improving data accuracy by 20%.
Executed and monitored clinical trials in accordance with Good Clinical Practice (GCP), improving regulatory compliance by 30%.
Coordinated with clinical operations for protocol development, resulting in a time-saving of 2 months per protocol.
Merck February 2018 - July 2018
Clinical Trials Assistant
Supported preparation of Clinical Review Forms (CRFs) for 10 Therapeutic Areas, enhancing the smooth transition into clinical trials.
Aided the coordination of clinical trials, contributing to 10% increase in number of successful clinical trials carried out.
Resume Worded Academic Center February 2021
Advanced Certificate in Clinical Research
Coursework in Epidemiology and Clinical Research Ethics
Resume Worded University June 2018
Master of Science - Biology
Specialized in Medical and Molecular Biology
Master's Thesis: 'Advances in Clinical Trial Protocols'
Clinical Research: Clinical Trial Design, Clinical Data Management, Regulations Compliance, Scientific Writing
Software: Oracle Clinical, Medidata Rave, SAS/STAT, Microsoft Office Suite (Excel, PowerPoint, Word)
Biomedical Techniques: Molecular Biology Techniques, Cell Culture, Bioinformatics, Microscopy, PCR
Certifications: Certified Clinical Research Coordinator (CCRC), Good Clinical Practice (GCP) Certification
Memberships: Member, Association of Clinical Research Professionals (ACRP)
Volunteering: Volunteer, Health Medical Camps for Underserved Populations (2016-2019)
Presentations: Presented research findings at 2020 Global Clinical Trials Conference
Your Name
Clinical Trial Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded April 2021 - Present
Clinical Trials Director
Spearheaded a division of Clinical Trial Managers, increasing productivity by 35%.
Established strong CRO management standards, resulting in 15% improved outcomes for outsourced clinical trials.
Orchestrated successful clinical development in oncology, leading to 3 patent applications.
Managed 8 regulatory submissions to U.S. Food and Drug Administration (FDA), ensuring 100% compliance.
Supervised the design and administration of Clinical Trial Management System (CTMS), leading to improved data reliability. August 2018 - March 2021
Clinical Trial Manager
Monitored 8 clinical trial protocols, reducing supposed protocol violations by over 20%.
Ensured strict adherence to Standard Operating Procedure (SOP) in clinical operations, raising compliance level by 15%.
Managed the use of Electronic Data Capture (EDC) systems in data handling, increasing data accuracy by 20%.
Eli Lilly and Company March 2017 - August 2018
Clinical Research Associate
Oversaw clinical data management for 5 trials, improving data validation process by 15%.
Collaborated with team members for effective clinical site monitoring of 4 sites, ensuring compliance with study protocols.
Handled regulatory submissions for 3 clinical trials ahead of schedule, enhancing the efficiency of the process by 10%.
Resume Worded University January 2019
Master of Science in Clinical Research
Specialized in Clinical Trial Design and Bioethics
Resume Worded Academic Center November 2016
Certified Clinical Research Professional (CCRP)
Accredited by the Society of Clinical Research Associates (SoCRA)
Clinical Research: Designing and Conducting Clinical Trials, Regulatory Compliance, Patient Recruitment, Data Analysis, Site Monitoring, Report Writing
Technologies and Tools: SPSS, EDC Systems, Medical Imaging Software, TrackWise (Proficient), ClinTrial, Oracle Clinical
Languages: English (Native), Spanish (Conversational)
Certifications: Advanced Certificate in Good Clinical Practice (GCP)
Awards: Awarded 'Clinical Trial Manager of the Year' at, 2020
Volunteering: Volunteer at Cure for Cancer Foundation - helping with patient advocacy initiatives
Professional Development: Attended annual ASCO Meetings and Conferences since 2017, completing multiple continued education requirements
Your Name
Clinical Trial Specialist
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded January 2022 - Present
Clinical Trial Specialist
Coordinated 15+ clinical trial activities across multiple sites, employing efficient Clinical Trial Management System (CTMS) utilization, boosting throughput by 18%
Authored and revised 20+ Standard Operating Procedures (SOPs) in alignment with Good Clinical Practice (GCP) guidelines, enhancing regulatory compliance by 27%
Executed effective CRO Management strategies, expediting the process of trial data acquisition and reducing backlog by 22%
Utilized Electronic Data Capture (EDC) systems to expedite data collection, improving overall data accuracy by 45%
Managed and trained a team of 12 clinical research associates, elevating team productivity by 30% and reducing turnover May 2018 - December 2021
Clinical Research Associate
Implemented innovative clinical research methodologies, increasing successful trial completion by 26%
Performed meticulous monitoring of 40+ clinical trials, maintaining stringent adherence to protocols and regulatory requirements
Contributed to biotechnology research, facilitating the submission of 10+ regulatory documents to the Institutional Review Board (IRB)
Johnson & Johnson November 2015 - April 2018
Clinical Research Coordinator
Steered clinical operations of 20+ trials for various oncology medicines, contributing to the positive results in 40% of the trials
Played a key role in IRB meetings, effectively communicating trial protocols and securing swift approvals
Managed patient consent process to meet ethical guidelines, minimizing consent dispute cases by 90%
Resume Worded Academic Center December 2021
Certification in Clinical Trial Management
Part-time certification while working at
Resume Worded University October 2015
Master of Science in Clinical Research
Specialization in Clinical Trial Design, Management and Regulatory Affairs
Clinical Research: Phase I – IV Trials, Protocol Development, Patient Recruitment, Data Analysis (Advanced)
Research Softwares: Oracle Clinical, Medidata Rave, SAS, REDCap, ClinCapture
Regulatory Compliance: ICH GCP, US FDA Regulations, EU Clinical Trial Directives, Quality Assurance
Bio-statistical Tools: SPSS, STATA, Matlab, R
Certifications: Certified Clinical Research Professional (CCRP) - May 2018
Leadership & Volunteering: Vice President - Clinical Research Society (2014 - 2015)
Projects: Conducted independent research on optimization of patient retention in clinical trials (Published research paper in Clinical Trials Journal, 2016)
Continuous Learning: Attended '2020 Clinical Trials Conference' – Updated knowledge about the latest industry trends and regulatory changes
Your Name
Clinical Research Associate
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE May 2019 - Present
Clinical Research Associate
Spearheaded protocol development efforts for 20+ clinical trials, resulting in an improvement of 37% in trial accuracy and efficiency
Streamlined relevant clinical data management processes, thereby increasing data reliability by 35%
Integrated multiple EDC systems, leading to a 50% reduction in data error rates
Managed patient recruitment and enrollment procedures, leading to a 30% increase in participant numbers in clinical trials
Provided critical feedback for the improvement of the Clinical Trial Management System (CTMS), significantly increasing its functionality and user-friendliness over time
Pfizer October 2015 - April 2019
Clinical Project Manager
Led the successful planning and execution of 10+ international clinical trials, improving drug recall rates by 25% through effective CRO Management
Developed a compliance tracking system eliminating protocol deviations by 27%
Successfully acquired IRB approvals for all assigned oncology clinical research studies
Resume Worded Institute May 2019
Certified Clinical Research Associate (CCRA)
Awarded following rigorous examination and practical assessment
Resume Worded University October 2015
Master of Clinical Research
Emphasis on pharmaceutical and biotechnical product development, patient-centered research methodologies, ethical considerations in clinical research and advanced statistical analysis
Clinical Research: Protocol development, Clinical monitoring, Regulatory compliance, Data collection and analysis, Quality Assurance, Risk Management
Software: MS Office Suite, ClinCapture, OpenClinica, CTMS, SPSS, SAS
Project Management: Risk Assessment, Stakeholder Management, Budgeting, Contract Negotiation, Time Management, Decision Making
Regulations & Standards: Good Clinical Practice (GCP), FDA regulations, ICH guidelines, Code of Federal Regulations Title 21, SOP
Certifications: Good Clinical Practice (GCP) Certification, Certified Clinical Project Manager (CCPM)
Professional Development: Active participant in 'Clinical Researcher Connect' - a platform for sharing industry insights and latest developments in clinical research
Volunteering: Serve as Mentor for 'Future Clinical Research Leaders' Initiative, guiding aspiring students in the field
Languages: English (Native), Spanish (Conversational)
Your Name
Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded February 2020 - Present
Clinical Research Coordinator
Managed budgets of 20+ clinical trials, securing additional funds for 30% of projects through strategic negotiations
Expeditiously addressed regulatory affairs issues, reducing processing time by 47%
Implemented a new follow-up protocol, leading to a 35% increase in patient retention
Processed and submitted 15+ regulatory submissions accurately and promptly, improving regulatory compliance
Implemented innovative clinical development strategies, leading to faster trial completion and 20% cost savings
Eli Lilly and Company September 2016 - January 2020
Clinical Trial Assistant
Reviewed and verified 500+ patient files, rectifying data inconsistencies and ensuring 100% adherence to the informed consent process
Efficiently used CTMS to track 50+ clinical trials simultaneously, improving data handling accuracy by 45%
Resume Worded Institute March 2020
Certified Clinical Research Coordinator (CCRC)
Included modules on clinical data management, study initiation and regulatory compliance
Resume Worded University August 2016
Bachelor of Science in Biological Sciences
Specialized in Genetics and Cell Biology
Thesis: The Impact of Clinical Trials on Patient Outcome
Clinical Data Management Tools: Medidata Rave, OpenClinica, REDCap, Oracle Clinical, Clinical Conductor, MATLAB
Proficiency in: ICH-GCP guidelines, trial execution, patient recruitment
Software: MS Office Suite, Adobe Acrobat Pro, Project Management Software (Trello, Jira)
Languages: English (Native), Spanish (Advanced), French (Basic)
Certifications: CITI Program Human Subjects Research (HSR) certification
Leadership & Volunteering: Volunteer, Health Care for the Homeless, Helped set up health clinics
Projects: Developed an effective patient recruitment strategy for a global trial, resulting in 30% increase in enrolment

How do I add skills to a Clinical Research Associate resume?

Review the job posting closely.

Go through the Clinical Research Associate posting you're applying to, and identify hard skills the company is looking for. For example, skills like Electronic Data Capture (EDC), Good Clinical Practice (GCP) and Clinical Development are possible skills. These are skills you should try to include on your resume.

Add industry skills like Protocol and Clinical Trials.

Add other common skills from your industry - such as Clinical Research, Clinical Trial Management System (CTMS) and Clinical Monitoring - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like Clinical Research Associates, Oncology Clinical Research and Clinical Site Monitoring - into your work experience too. This shows hiring managers that you have practical experience with these tools, techniques and skills.

Include examples of your research experience.

Consider including a section in your resume dedicated to your research experience. On Clinical Research Associate resumes, hiring managers want to see research projects which you led or where involved with, and their outcomes.

Use the exact job title.

Try to add the exact job title, Clinical Research Associate, somewhere into your resume to get past resume screeners. See the infographic for how to do this.

Word Cloud for Clinical Research Associate Skills & Keywords

The following word cloud highlights the most popular keywords that appear on Clinical Research Associate job descriptions. The bigger the word, the more frequently it shows up on employer's job postings. If you have experience with these keywords, include them on your resume.

Top Clinical Research Associate Skills and Keywords to Include On Your Resume

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Clinical Research Associate Resume Templates

Here are examples of proven resumes in related jobs and industries, approved by experienced hiring managers. Use them as inspiration when you're writing your own resume. You can even download and edit the resume template in Google Docs.

Resume Example
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Browse Skills from Similar Jobs

Frequently Asked Questions

What are the top skills you should add to your Clinical Research Associate resume?

On top Clinical Research Associate resumes, skills like Good Clinical Practice (GCP), Clinical Monitoring, Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), Clinical Trials, Clinical Research, Protocol and Clinical Development appear most often.

Depending on the exact role you're applying to, skills like Clinical Research Associates, Regulatory Submissions, Clinical Site Monitoring, Oncology Clinical Research and CRO Management can also be effective keywords to include on your resume.

Target your Resume to a Job Description

While the keywords above are a good indication of what skills you need on your resume, you should try to find additional keywords that are specific to the job. To do this, use the free Targeted Resume tool. It analyzes the job you are applying to and finds the most important keywords you need on your resume.

It is personalized to your resume, and is the best way to ensure your resume will pass the automated resume filters.

Start targeting your resume

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