Clinical Research Scientist

Clinical Research Scientist Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Clinical Research Scientist 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
  • Clinical Trials
  • Good Clinical Practice (GCP)
  • Clinical Development
  • Clinical Research
  • Drug Development
  • Oncology
  • Biotechnology
  • Clinical Monitoring
  • Life Sciences
  • Regulatory Submissions
  • CRO Management
  • Medical Writing
  • Clinical Trial Management System (CTMS)
  • Protocol
  • Electronic Data Capture (EDC)
  • XML Schema Definition (XSD)
  • U.S. Food and Drug Administration (FDA)
  • Molecular Biology
  • Medical Affairs
  • Clinical Study Design
  •   Show full list

Resume Skills: Clinical Research

  • Clinical Trial Management
  • Patient Recruitment
  • Clinical Trial Protocol
  • Adverse Event Reporting
  • FDA Guidelines
  • GCP Standards
  • Trial Design
  • Data Collection and Analysis
  • Medical Writing
  • FDA Regulations
  • Clinical Study Reports (CSRs)

Resume Skills: Software Proficiency

  • Oracle Clinical
  • Medidata Rave
  • EDC Systems
  • SPSS
  • SAS
  • MS Office Suite
  • CTMS
  • CDMS
  • EDC

Resume Skills: Medical Writing

  • Clinical Study Reports (CSRs)
  • Regulatory Submissions
  • Manuscripts
  • FDA Briefing Documents

Resume Skills: Software & Applications

  • Microsoft Office Suite
  • Adobe Acrobat
  • EndNote
  • GraphPad Prism
  • ChemDraw

Resume Skills: Standards & Guidelines

  • AMA Style

Resume Skills: Technical

  • Data Analysis
  • Epidemiology
  • Toxicology
  • Pharmacodynamics

Resume Skills: Biostatistical Analysis

  • SPSS
  • SAS
  • R
  • Python (Pandas, Numpy, Matplotlib, Seaborn)

Resume Skills: Medical Knowledge

  • Pharmacovigilance
  • Oncology
  • Gastroenterology
  • Cardiology
  • Infectious Diseases
  • Psychiatry

Resume Skills: Other Technical

  • Medical Writing
  • Data Management
  • Microsoft Office Suite (Word, Excel, PowerPoint)
  • IRB Applications
  • EDC Systems

Resume Skills: Statistical Modeling and Analysis

  • Survival Analysis
  • Longitudinal Data Analysis
  • Predictive Modeling
  • Multivariate Analysis
  • Regression Models
  • Hypothesis Testing

Resume Skills: Certifications

  • Certified Clinical Data Manager (CCDM)
  • Good Clinical Practice (GCP) Certification

Resume Skills: Clinical Regulatory Standards

  • GCP
  • ICH guidelines
  • FDA
  • EMA

Resume Skills: Project Management

  • MS Project
  • Risk Management
  • Quality Management
  • Resource Allocation

Resume Skills: Reporting & Data Analysis Tools

  • Excel
  • Tableau
  • Power BI
  • SQL
  Does your resume contain all the right skills? Paste in your resume in the AI Resume Scan ↓ section below and get an instant score.

Sample Clinical Research Scientist Resume: 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
Medical Writer
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded March 2020 - Present
Senior Medical Writer
Drafted Clinical Development Plans for 4 new drugs, leading to successful regulatory submissions to the FDA within 18 months.
Leveraged expertise in Molecular Biology to synthesize complex data into accessible documents, enhancing stakeholders' understanding.
Coordinated with multidisciplinary teams to prepare clinical study protocols, streamlining the clinical trial setup by 30%.
Provided medical writing training for new hires, improving department efficiency by 20%.
Used Biotechnology knowledge to write 10 in-depth reviews, increasing citations by 25%.
AstraZeneca January 2017 - February 2020
Medical Writer
Played a key role in publishing 20+ research papers in top-tier journals, expanding company's presence in academic communities.
Aided in drafting regulatory documents, with no major queries from regulatory agencies during review.
Contributed to writing clinical trial reports, ensuring data accuracy over 98%. June 2015 - December 2016
Clinical Research Associate
Managed Clinical Research documentation, guaranteeing compliance with international guidelines at all phases of the trials.
Gained hands-on experience with Clinical Trials, improving understanding and application of Good Clinical Practices (GCP).
Assisted in managing CRO, reducing project delivery timeline by 15%.
Resume Worded Academic Center May 2015
Master of Science - Biomedical Science
Concentration in Medical Writing & Communication
Resume Worded University May 2013
Bachelor of Science - Biological Sciences
Minor in Chemistry
Dean's List 2011, 2012 & 2013 (Top 10%)
Medical Writing: Clinical Study Reports (CSRs), Regulatory Submissions, Manuscripts, FDA Briefing Documents
Software & Applications: Microsoft Office Suite, Adobe Acrobat, EndNote, GraphPad Prism, ChemDraw
Standards & Guidelines: ICMJE, CONSORT, STROBE, PRISMA, AMA Style
Technical Skills: Data Analysis, Epidemiology, Toxicology, Pharmacodynamics
Certifications: American Medical Writers Association (AMWA) - Essential Skills Certificate, Certified Medical Publication Professional (CMPP)
Professional Affiliations: Member, American Medical Writers Association (AMWA), Member, International Society for Medical Publication Professionals (ISMPP)
Volunteering: Science Communication Volunteer, Local Non-profit Health Charity, Mentoring New Science Graduates at Resume Worded University
Your Name
Clinical Trial Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded April 2021 - Present
Clinical Trial Manager
Implemented integrated Clinical Trial Management System (CTMS), elevating data accuracy by 95% and optimizing trial efficiencies.
Spearheaded 5 multinational clinical trials in Oncology, ensuring successful data capture and regulatory submissions.
Led Medical Affairs team for the Oncology franchise, delivered presentations to healthcare professionals and patients successfully.
Overseen clinical protocols, ensuring adherence and reducing protocol deviations by 40%.
Managed budget effectively, achieving cost savings of $2 million during financial year 2021-22.
Novartis February 2018 - March 2021
Lead Clinical Research Associate
Played a key role in 10+ clinical studies, ensuring adherence to protocol and GCP.
Monitored spending and helped reduce project costs by 30%.
Managed CRO, streamlining communication and raising productivity by 20%. June 2015 - January 2018
Clinical Research Associate
Expedited data collection process using Electronic Data Capture (EDC) systems, causing data entry backlog to drop by 15%.
Managed Clinical Research documentation, improving consistency across all team documents.
Assisted in managing clinical trials, maintaining project timeline and quality standards.
Resume Worded Institute February 2018
Clinical Research Certification
Awarded for demonstrating superior skills in clinical research and trial management
Resume Worded University May 2015
Master of Science in Clinical Research
Focus on Clinical Trial Design and Administration
Honors: Cum Laude
Research Design Software: CTMS, CDMS, EDC, Oracle Clinical, Medidata Rave, SAS
Clinical Regulatory Standards: GCP, ICH guidelines, HIPAA, FDA, EMA
Project Management: MS Project, Risk Management, Quality Management, Resource Allocation
Reporting & Data Analysis Tools: Excel, Tableau, Power BI, SQL
Certifications: Certified Project Manager - Project Management Institute
Memberships: Member of the Society for Clinical Research Associates
Leadership & Volunteering: Volunteer Team Lead - Annual Clinical Research Charity Run
Continuous Learning: Attended 3+ industry conferences annually for the latest trends in clinical research

Compare Your Resume To These Clinical Research Scientist 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.

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

Review the job posting closely.

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

Add industry skills like Biotechnology and Clinical Monitoring.

Add other common skills from your industry - such as Clinical Development, Clinical Trials and Drug Development - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like U.S. Food and Drug Administration (FDA), Medical Affairs and XML Schema Definition (XSD) - into your work experience too. This shows hiring managers that you have practical experience with these tools, techniques and skills.

Emphasize your ability to solve problems.

Recruiters want to know that you're the kind of person that can solve new and challenging problems. In your Clinical Research Scientist resume, highlight projects that involved problems that were technically complex or mattered to the company.

Show evidence of your analytical skills.

Analytical skills involve your ability to break down a problem and come up with effective solutions. On Clinical Research Scientist resumes, hiring managers want to see evidence of how you analyzed quantitative or qualitative data.

Use the exact job title.

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

Word Cloud for Clinical Research Scientist Skills & Keywords

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

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Clinical Research Scientist 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
Clinical Research Assistant

Resume Example
Laboratory Research Assistant

Resume Example
Graduate Research Assistant

Resume Example
Chemistry Research Student

Resume Example
Policy and Research Policy Analyst

Resume Example
Equity Research Associate

Browse Skills from Similar Jobs

Frequently Asked Questions

What skills should you put on a Clinical Research Scientist resume?

Some effective Clinical Research Scientist skills you can add to your resume include:

  • Clinical Trials
  • Good Clinical Practice (GCP)
  • Clinical Development
  • Clinical Research
  • Drug Development
  • Oncology
  • Biotechnology
  • Clinical Monitoring

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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