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
  •  Find out what your resume's missing
  • 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)
  •  Match your resume to these skills

Resume Skills: Software Proficiency

Resume Skills: Medical Writing

Resume Skills: Software & Applications

Resume Skills: Standards & Guidelines

Resume Skills: Technical

Resume Skills: Biostatistical Analysis

Resume Skills: Medical Knowledge

Resume Skills: Other Technical

Resume Skills: Statistical Modeling and Analysis

Resume Skills: Certifications

Resume Skills: Clinical Regulatory Standards

Resume Skills: Project Management

Resume Skills: Reporting & Data Analysis Tools

  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 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.

Sample Clinical Research Scientist 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
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
Your Name
Clinical Research Manager
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE January 2020 - Present
Clinical Research Manager
Capitalized on clinical research expertise to secure approval for 6+ FDA-regulated trials, leading to advancement in key therapeutic areas.
Fostered a strong collaboration with the Institutional Review Board (IRB) to ensure timely study approval and adherence to Good Clinical Practice (GCP).
Implemented a Clinical Trial Management System (CTMS) to streamline operational efficiency, reducing trial execution time by 35%.
Led a team of researchers in managing upward of 20 complex oncology trials in alignment with clinical development goals.
Structured regulatory submissions to enhance approval rates, securing 5 successful submissions in the first quarter of 2021.
Resume Worded July 2015 - December 2019
Senior Clinical Research Associate
Managed site initiation, routine monitoring and close out visits for 30+ clinical studies in therapeutic areas.
Conducted compliance audits aligned with Standard Operating Procedures (SOPs); results enhanced the department’s audit score by 20%.
Leveraged Electronic Data Capture (EDC) systems to streamline data management and improve accuracy by 30%.
Pfizer April 2010 - June 2015
Clinical Research Associate
Coordinated with cross-functional teams to develop protocols, enhancing the success of clinical trials.
In collaboration with CROs, managed the study start-up process and successful enrollment of 90% of targeted patients.
Developed and maintained trial master files ensuring 100% completeness and accuracy.
Resume Worded Academic Center June 2009
Master of Science in Clinical Research
Emphasis on Advanced Clinical Trials Design
Resume Worded University May 2007
Bachelor of Science in Biomedical Science
Minor in Biostatistics
Dean's List 2005-2007
Clinical Research: Clinical Trials, Patient Recruitment, Drug Development, Protocol Development, Clinical Supervision
Software: Oracle Clinical, Medidata Rave, MS Office Suite, ClinCapture, REDCap
Regulation: GCP (Good Clinical Practices), IRB Compliance, FDA Regulations, EMEA Guidelines
Skills: Data Collection and Analysis, Risk Management, Project Management, Quality Assurance
Certifications: Certified Clinical Research Associate – Association of Clinical Research Professionals (ACRP), 2018
Awards: ‘Outstanding Clinical Research Manager’ –, 2021
Volunteering: Medical Volunteer – Doctors Without Borders, 2017-Present
Professional Affiliations: Member - Society of Clinical Research Associates, 2010-Present
Your Name
Clinical Trials Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded March 2021 - Present
Clinical Trials Manager
Streamlined process for clinical research, acquiring FDA approval for 4 key trials within a span of 6 months.
Introduced a user-friendly Clinical Trial Management System (CTMS) that increased efficiency by 40%.
Managed major oncology trials, ensuring alignment with clinical development strategies.
Augmented collaboration with the Institutional Review Board (IRB), ensuring strict adherence to Good Clinical Practice (GCP).
Leveraged biotechnology expertise to aid in regulatory submissions, earning 3 successful submissions in the past 6 months. August 2016 - February 2021
Senior Clinical Research Associate
Administered site initiation, routine monitoring and close out visits for 25+ clinical studies.
Implemented Standard Operating Procedures (SOPs), enhancing audit scores by 10%.
Utilized Electronic Data Capture (EDC) systems to improve data accuracy, reducing data discrepancies by 25%.
Johnson & Johnson January 2011 - July 2016
Clinical Research Associate
Partnered with teams to develop successful protocols, thereby increasing the success rate of trials.
Managed the study start-up process with CROs, exceeding patient enrolment targets by 80%.
Maintained and updated trial master files, achieving an accuracy score of 99%.
Resume Worded University March 2021
Ph.D. in Clinical Research
Cognate area: Biostatistics
Resume Worded Institute August 2016
Master of Science - Clinical Investigation
Received 'Best Student Award' for highest annual academic grade
Clinical Research: GCP, Protocol Design, Patient Recruitment, Data Monitoring
Regulatory Compliance: FDA Regulations, ICH Guidelines, Compliance audits, IRB Approvals
Technical Skills: MS Office, SPSS, SAS, EDC Systems, CTMS
Certifications: Certified Clinical Data Manager (2020), Professional Certification in Clinical Trials (2019)
Projects: Conducted 'Efficacy of Flu Vaccines' research - Worked in team of 5 to recruit 500+ participants, analyzed data using SAS
Leadership & Volunteering: Founded 'Research for Health', a non-profit organization promoting awareness about clinical research in community
Awards & Honors: Received 'Trailblazer Award' at Johnson & Johnson for remarkable performance in a complex clinical trial
Your Name
Clinical Research Project Manager
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE April 2019 - Present
Clinical Research Project Manager
Led the approval process of 7+ FDA-regulated trials, contributing to advancement in multiple therapeutic areas.
Collaborated effectively with the Institutional Review Board (IRB), ensuring robust compliance with Good Clinical Practice (GCP).
Integrated a Clinical Trial Management System (CTMS), improving operational efficiency by 45%.
Oversaw a team of researchers in conducting 15+ complex oncology trials in harmony with clinical development strategies.
Managed regulatory submissions to improve approval rates, securing 4 successful submissions in 2020.
Resume Worded December 2014 - March 2019
Senior Clinical Research Associate
Monitored and supervised 35+ clinical studies across various therapeutic areas.
Implemented audits in accordance with Standard Operating Procedures (SOPs), boosting the department’s audit score by 15%.
Used Electronic Data Capture (EDC) systems to enhance data management, increasing data accuracy by 20%.
Novo Nordisk February 2009 - November 2014
Clinical Research Associate
Coordinated with multi-disciplinary teams in development of protocols, boosting success rate of clinical trials.
Managed the study start-up process, accomplishing 85% of patient enrollment targets through effective collaboration with CROs.
Developed and maintained trial master files, achieving 95% data accuracy.
Resume Worded Institute December 2013
Master of Science in Clinical Research
Graduated summa cum laude, with a focus on Project Management in Clinical Research
Resume Worded University May 2008
Bachelor of Science in Biotechnology
Minors in Bioinformatics and Molecular Genetics
Ranked in top 10% of the class
Clinical Research: Clinical Trials Management, Protocol Design, Human Ethics Clearance, Patient Recruitment, Statistical Analysis, Risk Assessment
Administration & Policy Compliance: FDA Regulatory Requirements, Good Clinical Practices (GCP), Standard Operating Procedures (SOPs), Quality Assurance, Data Management, Safety Reporting
Project Management: Strategic Planning, Project Coordination, Resource Allocation, Conflict Resolution, Reporting, Stakeholder Engagement
Software Proficiency: Microsoft Office, Clinical Conductor CTMS, Medidata Rave, Oracle Clinical, REDCap, SPSS
Certifications: Project Management Professional (PMP) Certification (2019), Certified Clinical Research Professional (CCRP) (2015)
Volunteering: Medical Research Volunteer, Resume Worded Cancer Research Institute (2014 - 2018)
Awards: Outstanding Research Professional Award, Resume Worded Academic Center (2015)
Professional Memberships: Member, Association of Clinical Research Professionals (ACRP), Society of Clinical Research Associates (SOCRA)

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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