Research Study Coordinator

Research Study Coordinator Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Research Study Coordinator 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 Research
  • Clinical Trials
  • Good Clinical Practice (GCP)
  • REDCap
  • Institutional Review Board (IRB)
  • Public Health
  • Data Collection
  •  Find out what your resume's missing
  • Healthcare
  • Medical Research
  • Electronic Data Capture (EDC)
  • Qualitative Research
  • Research
  • Oncology
  • Epic Systems
  • Data Analysis
  • Phlebotomy
  • Electronic Medical Record (EMR)
  • Community Outreach

  •   Show full list

Resume Skills: Clinical

  • ICH/GCP Guidelines
  • Clinical Trial Protocols
  • Adverse Event (AE) Management
  • Patient Recruitment
  • Data Management
  • Site Monitoring
  • Informed Consents
  • Data Interpretation
  • HIPAA Compliance
  •  Match your resume to these skills

Resume Skills: Scientific Software

Resume Skills: Administrative

  • Microsoft Office (Excel, Word, PowerPoint)
  • Time Management
  • Medical Terminology
  • Multi-Site Coordination
  • Patient Scheduling
  • Budget Management
  • Contract Negotiation
  • Project Management
  • Scheduling
  • Material management
  • GCP
  •  Match your resume to these skills

Resume Skills: Research

Resume Skills: Languages

Resume Skills: Trials Management

Resume Skills: Data Analysis

Resume Skills: Communication and Interpersonal

  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 Research Study Coordinator 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 Research Study Coordinator 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
Research Study Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded January 2022 - Present
Senior Research Coordinator
Managed a team of 5 junior coordinators, successfully improving project completion time by 20% contributing to overall efficiency
Mastered Good Clinical Practice (GCP) in the planning of 7 key clinical trials; increased accuracy of data collection by 15% enhancing overall research precision
Revolutionized data analysis protocols using IBM SPSS, enhancing data integrity and decreasing error rates by 40%
Johnson & Johnson January 2020 - December 2021
Research Associate
Leveraged Electronic Data Capture and REDCap to streamline data collection for 8 clinical trials, improving data quality by 18%
Implemented Electronic Medical Record system improving patient data organization which reduced retrieval time by 30%
Promoted implementation of Epic Systems for clinical processes improving collaboration and staff efficiency by 25% January 2018 - December 2019
Clinical Research Assistant
Assessed and improved review board processes with IRB, reducing administration time by 20%
Facilitated community outreach programs for 2000+ local residents promoting public health awareness
Resume Worded University May 2017
Master of Science - Clinical Research
Focused on Bio-statistical methods and epidemiology
Resume Worded Academic Center December 2017
Certificate in Clinical Research Coordination
Completed part-time while working as a clinical research assistant
Trials Management: Clinical trials design, IRB protocols, FDA regulations, Patient recruitment
Data Analysis: SPSS, STATA, SAS, Microsoft Excel, Data validation, Statistical report writing
Administrative Skills: Budget Management, Contract Negotiation, Project Management, Scheduling, Material management, GCP
Communication and Interpersonal Skills: Cross-functional Team Leadership, Relationship Building, Clear Oral and Written Communication
Certifications: Certified Clinical Research Coordinator (CCRC) - ACRP, Certified Clinical Research Professional - SOCRA
Volunteering: Health Care Volunteer – Local Senior Home, Event Organizer – Annual Medical Charity Run
Projects: Led team to successful completion of a multi-center randomized control trial investigating the efficacy of medication X
Professional Development: Participated in regular GCP and ICH regulation seminars and workshops
Your Name
Clinical Program Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE June 2020 - Present
Clinical Program Coordinator
Led a 10-member team in the implementation of clinical programs, boosting patient enrollment by 35%
Developed robust qualitative research methodologies, enhancing research quality and improved results accuracy by 22%
Streamlined clinical trial processes, reducing resource wastage and operational costs by 30% with a keen insight on public health considerations
Pfizer January 2019 - May 2020
Research Study Associate
Pioneered a new Electronic Data Capture (EDC) process reducing clinical data errors by 33%
Advanced the application of Good Clinical Practice (GCP) in 12 distinct clinical trials, which improved trial efficiency by 15%
Championed use of Epic Systems to streamline clinical data access improving staff productivity by 25%
Resume Worded June 2017 - December 2018
Junior Research Coordinator
Enhanced clinical processes using clinical research tools like EMR, reducing data redundancy by 20%
Improved community medical research participation by implementing community outreach programs for 1200+ local residents
Resume Worded Academic Center May 2017
Master of Science in Clinical Research
Emphasis on Epidemiology and Biostatistics
Thesis topic: 'Efficacy of New Clinical Trials: An Analytical Approach'
Resume Worded University May 2015
Bachelor of Science in Biological Sciences
Minors in Chemistry and Psychology
Dean's List
Research Skills: Epidemiological Research, Clinical Trials, Patient Interviews, Data Collection, Biostatistics
Scientific Software: SPSS, STATA, SAS, MS Office Suite, Nvivo
Clinical Skills: Patient Recruitment, Informed Consents, Data Interpretation, HIPAA Compliance
Languages: English (Native), Spanish (Fluent)
Certifications: Certified Clinical Research Coordinator (CCRC), ICH-GCP training completed
Awards & Achievements: Recognized with 'Performance Excellence Award' (2020) at for successfully coordinating a multi-phase clinical trial
Professional Memberships: Active member of the Association of Clinical Research Professionals (ACRP)
Volunteering & Service: Volunteer at local community health center, providing health outreach and education
Your Name
Clinical Trials Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded March 2021 - Present
Clinical Trials Coordinator
Enhanced clinical trials productivity by 30% through use of REDCap for advanced data collection and analysis
Led Good Clinical Practice (GCP) compliance across 8 trials, ensuring IRB goals were met and advanced trial efficiency by 15%
Boosted patient participation in oncology research trials by 40% through focused community outreach initiatives
Novartis February 2019 - February 2021
Research Project Associate
Transformed clinical data management practices by leveraging advanced IBM SPSS, enhancing research data quality by 30%
Improved EMR protocols, resulting in faster patient data retrieval and boosted productivity by 20%
Spearheaded implementation of Epic Systems for better clinical operations, resulting in streamlined clinical procedures and better team collaboration September 2017 - January 2019
Junior Clinical Research Coordinator
Performed phlebotomy with a success rate of 96% ensuring blood samples for clinical trials were accurately obtained
Facilitated successful data collection from electronic health records reducing errors by 25%
Resume Worded Institute April 2021
Certified Clinical Research Professional (CCRP)
Focused on essential clinical research regulations and guidelines, including GCP, ICH, and FDA regulations
Resume Worded University Aug 2017
Masters of Science - Clinical Research
Elective coursework in pharmaceutical biostatistics and drug development
Thesis: 'Efficient Strategies for Patient Enrollment in Clinical Trials'
Clinical Research: ICH/GCP Guidelines, Clinical Trial Protocols, Adverse Event (AE) Management, Patient Recruitment, Data Management, Site Monitoring
Administrative Skills: Microsoft Office (Excel, Word, PowerPoint), Time Management, Medical Terminology, Multi-Site Coordination, Patient Scheduling
Data Management and Statistics Software: SPSS, SAS, EpiInfo, Medidata, ClinTrial
Certifications: Good Clinical Practice (GCP) Certification (2018), HIPAA Compliance Training (2018)
Conferences & Memberships: Society of Clinical Research Associates Member (2016 - Present), Attendee at Annual SMART Trials Conference (2019 - Present)
Volunteering: Volunteer Clinical Researcher, Local Community Health Center (2015 - 2017)
Languages: English (Native), Spanish (Fluent), French (Conversational)
Your Name
Study Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded January 2022 - Present
Senior Study Coordinator
Spearheaded the implementation of Good Clinical Practice (GCP) protocols in clinical trials, resulting in 25% increase in study efficiency
Championed the use of REDCap for data collection and analysis, improving data integrity by 30%
Supervised a team of 5 study coordinators, providing training on Standard Operating Procedures (SOPs) and Good Laboratory Practice (GLP)
Proactively liaised with the Institutional Review Board (IRB) for study audits, achieving 100% compliance
Managed CRO relationships, ensuring alignment with study goals and timelines January 2019 - December 2021
Study Coordinator II
Coordinated all stages of 7 clinical trials in sync with protocols, culminating in the timely completion of each phase
Leveraged knowledge of Public Health and Life Sciences to develop effective recruitment strategies, tripling patient enrollment
Conducted Informed Consent process with study participants, ensuring transparency and ethical standards
Utilized the Clinical Trial Management System (CTMS) for seamless trial data management
Pfizer June 2016 - December 2018
Assistant Study Coordinator
Assisted in the coordination of 4 clinical trials, facilitating accurate data collection
Gained proficiency in Biotechnology and Toxicology research methodologies
Developed understanding of animal models used in the study of diseases
Resume Worded University May 2016
Master of Science in Clinical Research
Thesis: Impact of a Clinical Study Coordinator's Role in Facilitating Effective Clinical Trials
Resume Worded Institute May 2013
Bachelor of Science in Health Sciences
Concentration: Clinical Studies, Pharmaceutical Science and Management
Honors: Dean's List for 8 consecutive semesters
Clinical Research & IST Management: Epic Systems, Clarity, OnCore, REDCap, CITI program, IRB coordination, Patient recruitment protocols
Digital Health & eTrials: Electronic Data Capture (EDC), Interactive Response Technology (IRT), Remote Patient Diagnostics (RPM)
Project & Data Management: Microsoft Office - Excel, Word, PPT (Advanced), MS Project, SPSS, SAS, Data Privacy and Compliance
Languages: English (Native), French (Conversational)
Certifications: Certified Clinical Research Coordinator (CCRC) – ACRP, 2017
Leadership & Volunteering: Brownie Girl Scout Leader – Mentoring young girls (2013-2015)
Awards: Exceptional Performance Award – Pfizer, 2017
Publications: Co-author of 'Effective Clinical Study Practices' in Health Journal, 2018
Your Name
Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded March 2020 - Present
Lead Clinical Research Coordinator
Developed and executed clinical research projects, resulting in the publication of 5 research papers in peer-reviewed journals
Streamlined the standard operating procedures (SOPs), reducing data errors by 15%
Applied expertise in Healthcare and Life Sciences research methodologies to drive the progress of studies
Mentored a team of junior coordinators, fostering adherence to Good Laboratory Practice (GLP) for consistent results
Fostered strong relations with clinical research organizations (CRO), improving project delivery timelines by 20% May 2017 - February 2020
Clinical Research Coordinator
Managed lifecycle of clinical trial protocols, complying with Good Clinical Practice (GCP) guidelines
Supervised patient enrollment, ensuring informed consent was duly obtained
Implemented use of REDCap for efficient data management and analysis
Facilitated smooth audits from the Institutional Review Board (IRB), maintaining 100% compliance rate
Novartis January 2016 - April 2017
Clinical Research Assistant
Supported coordinators in Clinical Trial Management System (CTMS) usage for accurate trial data recording
Acquired expertise in Public Health and Biotechnology research methodologies
Assisted in the adherence to Standard Operating Procedures (SOPs)
Resume Worded University April 2020
Master's in Clinical Research
Courses in Clinical Data Management and Bio-Statistics
Resume Worded Academic Center December 2015
Bachelor of Science in Biology
Minors in Chemistry and Psychology
Recipient of the Academic Achievement Award in Biology
Research Methodologies: Quantitative and Qualitative Research, Double-Blind Studies, Patient Recruitment, Protocol Development
Clinical Trial Management Software: Medidata RAVE, Oracle Clinical, REDCap, OnCore Clinical Trial Management
Data Analysis: SPSS, SAS Analytics, Python, Matlab
Regulatory Compliance: FDA Regulations, Good Clinical Practice (GCP), ICH Guidelines
Certifications: Certified Clinical Research Coordinator (ACRP - 2018)
Continuing Education: Advanced Certificate in Clinical Trials Management (Merit Badge University -2023)
Professional Memberships: Member, Association of Clinical Research Professionals
Awards: Resume Worded's Clinical Research Award for Excellence (2019)
Your Name
Clinical Project Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded February 2019 - Present
Clinical Project Manager
Directed all aspects of clinical research projects, leading to successful completion of studies on time and within budget
Implemented robust data management systems such as REDCap, reducing data redundancy by 30%
Trained cross-functional team of 7 to adhere to Good Clinical Practice (GCP) and Good Laboratory Practice (GLP)
Presented research findings at international conferences, raising the profile of the organization in the scientific community
Liaised with CRO partners, ensuring alignment of goals and seamless collaboration October 2016 - January 2019
Clinical Research Coordinator
Orchestrated clinical trial protocols, leveraging knowledge of Public Health, Life Sciences and Biotechnology
Oversaw Informed Consent process, adhering to ethical considerations and regulatory guidelines
Utilized Clinical Trial Management System (CTMS) to efficiently manage trial data
Facilitated Institutional Review Board (IRB) audits, maintaining 100% compliance
Roche June 2014 - September 2016
Study Coordinator
Coordinated clinical trials diligently, ensuring adherence to SOPs and GCP
Contributed to the understanding of Toxicology and animal models in research
Ensured the ethical recruitment and enrollment of patients for study participation
Resume Worded University May 2014
Master's Degree in Clinical Research
Graduated with Honors
Resume Worded Institute May 2012
Bachelor of Science - Biomedical Science
Concentration in Clinical Research
Awards: Dean's List 2010-2012 (Top 10%)
Clinical Research: Patient Recruitment, Data Collection, Compliance & Ethics
Project Management: Risk Analysis, Project Scheduling, Resource Allocation
Data Management: Clinical Databases (e.g. EDC and eTMF), Quality Control, Data Analysis
Regulations & Standards: ICH/GCP, FDA Regulations, HIPAA Compliance
Certifications: Project Management Professional (PMP) - Certification (2022), Certified Clinical Data Manager (CCDM) - Certification (2020)
Volunteer Work: Clinical Coordinators Without Borders (Volunteer Clinical Coordinator - Thailand, 2015)
Leadership: Association of Clinical Research Professionals (ACRP) - Board Member, 2018-present
Courses: CRA & CRC Beginner's Guide, Certified Research Pharmacist

How do I add skills to a Research Study Coordinator resume?

Review the job posting closely.

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

Add industry skills like Clinical Trials and Institutional Review Board (IRB).

Add other common skills from your industry - such as Data Collection, Public Health and REDCap - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like Oncology, Qualitative Research and Data Analysis - into your work experience too. This shows hiring managers that you have practical experience with these tools, techniques and skills.

Show your ability to multitask.

Since you're going to be interfacing with different teams and people, Research Study Coordinator hiring managers expect you to be able to multitask, so it's a good idea to emphasize this skillset in your resume.

Include examples of your research experience.

Consider including a section in your resume dedicated to your research experience. On Research Study Coordinator 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, Research Study Coordinator, somewhere into your resume to get past resume screeners. See the infographic for how to do this.

Word Cloud for Research Study Coordinator Skills & Keywords

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

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Research Study Coordinator 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.

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Frequently Asked Questions

What skills should you put on a Research Study Coordinator resume?

On top Research Study Coordinator resumes, skills like Clinical Research, Clinical Trials, Good Clinical Practice (GCP), REDCap, Institutional Review Board (IRB), Public Health, Data Collection and Healthcare appear most often.

Depending on the exact role you're applying to, skills like Electronic Medical Record (EMR), Oncology, Electronic Data Capture (EDC), Qualitative Research and Data Analysis 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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