Clinical Trial Associate

Clinical Trial Associate Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Clinical Trial 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 Trial Management System (CTMS)
  • Clinical Trials
  • Electronic Data Capture (EDC)
  • Clinical Development
  • Clinical Research
  • Standard Operating Procedure (SOP)
  •  Find out what your resume's missing
  • Clinical Operations
  • CRO Management
  • Oncology
  • Protocol
  • Trial Master File (TMF)
  • Clinical Monitoring
  • Biotechnology
  • U.S. Food and Drug Administration (FDA)
  • Regulatory Affairs
  • Institutional Review Board (IRB)
  • Regulatory Submissions
  • Oncology Clinical Research
  • Informed Consent

  •   Show full list

Resume Skills: Regulations

Resume Skills: Clinical Research

  • Protocol Development
  • Data Management
  • Clinical Monitoring
  • Adverse Event Reporting
  • Patient Recruitment
  • Regulatory Submissions
  • Project Management
  • Regulatory Compliance
  • Safety Reports
  •  Match your resume to these skills

Resume Skills: Data Analysis & Statistics

Resume Skills: Softwares

Resume Skills: Technological Proficiency

  • MS Office Suite
  • PowerPoint
  • Excel
  • Clinical Data Management Systems (Medidata Rave, Oracle Clinical)
  • Statistical Analysis Software (SPSS, STATA)
  •  Match your resume to these skills

Resume Skills: Languages

  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 Trial 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 Trial 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.

Choose a template
Your Name
Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resumed Worded March 2018 - Present
Clinical Research Coordinator
Led a team in managing 15+ clinical trials concurrently, ensuring adherence to standard operating procedures.
Decreased patient follow-up time by 18% by implementing a robust Clinical Trial Management System (CTMS).
Spearheaded various oncology clinical research initiatives, driving advancements in cancer therapeutics.
Managed Trial Master File (TMF) document systems for 10+ trials concurrently, ensuring accurate and up-to-date documentation.
Developed training materials regarding regulatory affairs, enhancing compliance with FDA guidelines across the team. November 2015 – February 2018
Clinical Research Associate
Contributed to a 30% increase in clinical trial enrollment by improving the informed consent process.
Facilitated 20% quicker data capture by implementing an effective Electronic Data Capture (EDC) system.
Participated in several successful regulatory submissions, ensuring full compliance with FDA directives.
Johnson & Johnson June 2014 - October 2015
Clinical Research Assistant
Supported the clinical trials team in managing data, achieving a 99% accuracy rate.
Assisted in the execution of Good Clinical Practice (GCP) across all trials, ensuring high standards of research conduct.
Aided in the setup and maintenance of clinical operations, improving operational efficiency.
Resume Worded University May 2014
Master of Health Research - Clinical Trials
Specialization in Clinical Research Methodologies
Resume Worded Academic Center May 2012
Bachelor of Science - Biomedical Sciences
Minor in Medical Statistics
Awards: Dean's List (Top 10%)
Certifications: Certified Clinical Research Coordinator (CCRC), SOCRA Certified Clinical Research Professional
Professional Development: Attended Advanced Course on Clinical Trial Management & Regulatory Compliance (2020)
Volunteering: American Cancer Society - Conducted awareness campaigns and fund-raising events
Projects: Involved in a notable research project on cancer therapeutics that won an innovation grant
Your Name
Clinical Research Associate
City, Country  •  (123) 456-789  •  [email protected]  •
Resumed Worded February 2019 - Present
Clinical Research Associate
Managed 6 clinical trials from initiation to close-out, ensuring adherence to protocol and GCP.
Streamlined data management processes using Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS), improving trial efficiency by 28%.
Led liaison with Institutional Review Boards (IRB), securing necessary approvals for 100% of proposed trials.
Played a key role in achieving timely regulatory submissions, maintaining 100% compliance with FDA guidelines.
Successfully conducted site monitoring visits, ensuring all data collected were accurate and consistent. August 2016 - January 2019
Research Analyst
Reduced errors in data analysis by 22% with effective data quality initiatives.
Supported oncology-focused research projects, assisting in patient recruitment and data collection.
Maintained accurate study documentation and Trial Master Files (TMF), ensuring audit readiness.
Roche June 2015 - July 2016
Clinical Research Intern
Assisted in data management tasks, improving the accuracy of clinical trial data by 15%.
Contributed to creating a streamlined informed consent process, improving patient understanding and compliance.
Participated in maintaining consistent communication with CROs, enhancing the management of outsourced trials.
Resume Worded Institute January 2019
Certification in Clinical Research
Awarded for proficiency in clinical trial management
Resume Worded University June 2015
Bachelor of Science - Biomedical Sciences
Minors in Clinical Research and Data Analysis
Dean's List 2014 (Top 10%)
Clinical Research: Protocol Development, Data Management, Clinical Monitoring, Adverse Event Reporting, Patient Recruitment, Regulatory Submissions
Data Analysis & Statistics: SPSS, SAS, STATA, Python (Pandas, Numpy), SQL, Epidemiology
Softwares: Oracle Clinical, Medidata Rave, OpenClinica, Clinical Conductor, Inform
Regulations: GCP, ICH Guidelines, FDA, EMA
Certifications: Certified Clinical Research Professional
Professional Affiliations: Member of Association of Clinical Research Professionals
Awards & Recognitions: Employee of the year 2020 at Resumed Worded
Languages: English (Native), French (Conversational)

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

Review the job posting closely.

Go through the Clinical Trial Associate posting you're applying to, and identify hard skills the company is looking for. For example, skills like Clinical Research, Clinical Trial Management System (CTMS) and Clinical Development are possible skills. These are skills you should try to include on your resume.

Add industry skills like Good Clinical Practice (GCP) and Electronic Data Capture (EDC).

Add other common skills from your industry - such as Standard Operating Procedure (SOP), Clinical Operations and Clinical Trials - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like Regulatory Affairs, Oncology Clinical Research and Institutional Review Board (IRB) - into your work experience too. This shows hiring managers that you have practical experience with these tools, techniques and skills.

Use the exact job title.

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

Word Cloud for Clinical Trial Associate Skills & Keywords

The following word cloud highlights the most popular keywords that appear on Clinical Trial 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 Trial Associate Skills and Keywords to Include On Your Resume

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Clinical Trial 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
Operations Associate (Entry Level Operations Manager)

Resume Example
Sales Associate / Retail Salesperson

Resume Example
Regulatory Affairs Associate (Entry Level)

Resume Example
Sales Associate / Retail Salesperson

Resume Example
Sales Associate / Retail Salesperson

Resume Example
Clinical Trial Manager

Browse Skills from Similar Jobs

Frequently Asked Questions

What skills should you add to a Clinical Trial Associate resume?

Some effective Clinical Trial Associate skills you can add to your resume include:

  • Good Clinical Practice (GCP)
  • Clinical Trial Management System (CTMS)
  • Clinical Trials
  • Electronic Data Capture (EDC)
  • Clinical Development
  • Clinical Research
  • Standard Operating Procedure (SOP)
  • Clinical Operations

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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