Clinical Research Coordinator

Clinical Research Coordinator Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Clinical Research 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
  • Good Clinical Practice (GCP)
  • Clinical Research
  • Clinical Trials
  • Institutional Review Board (IRB)
  • Electronic Data Capture (EDC)
  • Informed Consent
  • Protocol
  •  Find out what your resume's missing
  • Oncology Clinical Research
  • Patient Recruitment
  • REDCap
  • Clinical Research Experience
  • Clinical Trial Management System (CTMS)
  • Healthcare
  • Clinical Data Management
  • Phlebotomy
  • Electronic Medical Record (EMR)
  • Public Health
  • Oncology
  • Medicine
  • Study Coordination
  • Life Sciences
  • Standard Operating Procedure (SOP)
  • Research Ethics
  • Research
  • Data Analysis
  • Hospitals
  • Regulatory Submissions

  •   Show full list

Resume Skills: Clinical Research

  • Clinical Trial Design
  • Clinical Data Management
  • Regulations Compliance
  • Scientific Writing
  • Protocol Development
  • Clinical Trial Management
  • Data Quality Control
  • Statistical Analysis
  • Regulatory Compliance
  • Risk Assessment
  • Clinical Trials Coordination
  • Clinical Trials Monitoring
  • Data Analysis (SAS, SPSS)
  • Clinical Trial Protocol
  • Quality Assurance and Control
  • FDA Compliance
  • Safety Monitoring
  • GCP Standards
  • Clinical Trials Administration
  • Quantitative and Qualitative Research
  • Double-Blind Studies
  • Patient Recruitment
  •  Match your resume to these skills

Resume Skills: Software

  • Oracle Clinical
  • Medidata Rave
  • Microsoft Office Suite (Excel, PowerPoint, Word)
  • OnCore CTMS
  • ClinVar
  • MedDRA (Coding Software)
  • Clinical Conductor
  • MS Office Suite
  • Adobe Acrobat Pro
  • Project Management Software (Trello, Jira)
  • REDCap
  • OpenClinica
  • SAS
  • SPSS
  • MS Office Suite (Advanced in Excel)
  • CTMS
  • Medidata RAVE
  • OnCore Clinical Trial Management
  •  Match your resume to these skills

Resume Skills: Regulatory Compliance

  • FDA Guidelines
  • NIH Guidelines
  • IRB Submissions
  • FDA Regulations
  • Good Clinical Practice (GCP)
  • ICH Guidelines
  • ICH-GCP Guidelines
  • Clinical Operations
  • Quality Assurance Practices
  •  Match your resume to these skills

Resume Skills: Data Management

Resume Skills: Data Analysis

  • SPSS
  • Clinical Data Management
  • Quantitative Analysis
  • Statistical Analysis
  • SAS Analytics
  • Python
  • Matlab
  • Quantitative Data Analysis
  • Qualitative Data Analysis
  • Biostatistics
  •  Match your resume to these skills

Resume Skills: Medical

Resume Skills: Language

Resume Skills: Clinical Data Management Tools

Resume Skills: Biomedical Techniques

Resume Skills: Clinical Research Methods

Resume Skills: Regulations & Practicalities

Resume Skills: Statistical Analysis

Resume Skills: Techniques

Resume Skills: Technical

Resume Skills: Analytical Tools

Resume Skills: Medical Proficiencies

Resume Skills: Proficiency in

Resume Skills: Medical Tools

Resume Skills: Tech

  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 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 Clinical Research 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
Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE January 2022 - Present
Clinical Research Coordinator
Streamlined patient recruitment procedures, resulting in a 30% increase in enrollment for clinical trials which significantly expedited trials launch.
Initiated and established a Clinical Trial Management System (CTMS) leading to an improvement in data capture and reporting efficiency by 40%.
Increased compliance with Good Clinical Practice (GCP) and Protocol guidelines by 50% through the strategic redesign of training workshops for research staff.
Enhanced patient education strategies, leading to a 20% surge in Informed Consent rates and improved patient engagement.
Managed cross-functional clinical research teams leading to a 25% increase in overall team productivity.
Resume Worded April 2019 - December 2021
Assistant Clinical Research Coordinator
Successfully coordinated with the Institutional Review Board (IRB), resulting in increased protocol approval rate.
Boosted clinical data management efficiency by incorporating Electronic Data Capture (EDC) tools into routine data collection and analysis procedures.
Synchronized health data retrieval from the Electronic Medical Record (EMR) system, enhancing data integrity by 35%.
Mayo Clinic June 2018 - March 2019
Clinical Research Intern
Supported the implementation of REDCap for efficient data collection, ensuring quality clinical data management.
Assisted in the development of a standard operating procedure for Phlebotomy, increasing work accuracy by 20%.
Contributed to public health research projects, resulting in two published studies in revered medical journals.
Resume Worded University May 2019
Master of Science in Clinical Research Management
Emphasis on Clinical Research methods and ethics
Resume Worded Academic Center April 2018
Bachelor of Science in Biology
Minors in Biochemistry and Biostatistics
Dean's List - 2016: Top 10% in class
Clinical Research Methods: Clinical Trials, Human Subject Protection, Clinical Study Design, Safety Reports, Risk Mitigation
Data Management: SPSS, SAS, Python, SQL, Data Analysis, Database Setup
Regulations & Practicalities: ICH-GCP, FDA Regulations, Ethics, Informed Consent, Research Protocols
Medical: Medical Terminology, Patient Assessment, Phlebotomy, Cardiopulmonary Resuscitation
Certifications: Certified Clinical Research Coordinator - Association of Clinical Research Professionals (2020), Good Clinical Practice certification - CITI (2019)
Projects: Led a team of interns in an investigative Research Study at Mayo Clinic in Mayo Clinic, produced a publishing-worthy statistical report
Professional Development: Continuous education participant - Annual Clinical Research Conferences
Volunteer Experience: Helping Hand - Medical aid to the homeless (2017-2018)
Your Name
Clinical Trials Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded February 2022 - Present
Clinical Trials Coordinator
Led the Oncology Clinical Research division, overseeing 12 trials and resulting in a 35% increase in successful outcomes.
Developed streamlined patient recruitment strategies, leading to a 40% boost in patient enrollment in trials.
Implemented Good Clinical Practice (GCP) strategies, improving clinical trials' conformity by 30%.
Introduced an efficient Clinical Trial Management System (CTMS) that saved up to 15 hours per week.
Managed overall Life Sciences research portfolio, leading to successful closure of 5 trials ahead of schedule. May 2019 - January 2022
Clinical Trials Assistant
Key player in achieving 100% compliance for Informed Consent obtained from trial participants.
Initiated Electronic Data Capture (EDC) use, slashing manual errors in data collection and recording by 30%.
Spearheaded three successful Pediatric trials, contributing to the approval of a crucial pediatric oncology drug.
MedStar Health April 2018 - April 2019
Healthcare Assistant Intern
Assisted with clinical data management including protocol and study coordination.
Contributed significantly to a ground-breaking Public Health study published in a Peer-reviewed Journal.
Coordinated with EMR and EDC systems, resulting in maintainance of accurate patient records.
Resume Worded University April 2022
Master of Science - Clinical Research and Trials
Emphasis in Clinical Trials Management and Data Analysis
Resume Worded Academic Center March 2018
Bachelor of Science - Public Health
Distinction of Major, Dean's List 2017 (Top 10%)
Clinical Research: Clinical Trials Coordination, Clinical Trials Monitoring, Regulatory Compliance, Data Analysis (SAS, SPSS)
Techniques: Quality Control, Data Verification, Therapeutic Area Expertise, Patient Recruitment, Study Files Management
Software: Oracle Clinical, OnCore CTMS, ClinVar, MedDRA (Coding Software), Medidata Rave, Clinical Conductor
Certifications: Certified Clinical Trials Coordinator (CCTC)
Professional Awards: Rising Star Award for exceptional contributions to clinical research projects
Volunteering: Local Health Clinic, Community Health Education Sessions Coordination
Continuous Learning: National Institutes of Health (NIH), Protecting Human Research Participants Course
Your Name
Clinical Research Manager
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE March 2022 - Present
Clinical Research Manager
Leveraged the CTMS, ensuring a 10% increase in system utilization, leading to more efficient study coordination.
Launched 12 clinical trials within the first quarter, faster than company average turnaround.
Increased the patient recruitment rate by 30% through active community outreach and partnering with local public health initiatives.
Introduced electronic Informed Consent practices, reducing paperwork by 60% and saving 5 hours per week.
Led cross-functional team of 15 clinical research staff, resulting in a 20% increase in productivity.
Resume Worded July 2019 - February 2022
Clinical Research Associate
Orchestrated Oncology Clinical Research projects, successfully closing 10 critical trials.
Maintained 100% compliance with GCP and Protocol, resulting in zero listed inaccuracies or breaches during audits.
Streamlined data collection via REDCap, improving data management efficiency by 25%.
Rush University Medical Center August 2018 - June 2019
Public Health Research Intern
Assisted in the preparation of Informed Consent documents following IRB guidelines.
Managed collection and entry of clinical trial data into the EDC system, ensuring optimum accuracy.
Played a vital role in a prominent Medicine research paper, contributing to the development of an impactful healthcare policy.
Resume Worded Institute May 2018
Master of Science - Clinical Research
Graduated with Honors, G.P.A. 4.0/4.0
Resume Worded University May 2016
Bachelor of Science - Public Health
Focused coursework in Epidemiology and Biostatistics
Award: Dean's List 2014-2016 (Top 10%)
Clinical Research: Protocol Development, Clinical Trial Management, Data Quality Control, Statistical Analysis, Regulatory Compliance, Risk Assessment
Software Proficiency: SPSS, SAS, Medidata Rave, Clinical Conductor, MS Office Suite (Advanced in Excel)
Statistical Analysis: Regression Analysis, Predictive Modelling, Hypothesis Testing, Data Visualization, Quantitative & Qualitative Research Techniques
Regulatory Understanding: FDA Regulations, ICH-GCP Guidelines, Clinical Operations, Quality Assurance Practices
Certifications: Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates (SoCRA)
Leadership & Volunteering: Public Health Volunteer, United Way (2017 - 2020); Organized semi-annual health awareness campaigns and free check-up camps
Professional Development: Attendee, Society for Clinical Research Sites (SCRS) Annual Conference (2018, 2019)
Awards: Outstanding Clinical Researcher, Resume Worded 2021; Recognition for excellence in clinical trial management and patient safety
Your Name
Clinical Research Nurse
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded February 2019 - Present
Clinical Research Nurse
Supervised a team of 6 in successfully monitoring 30+ clinical trials at various stages, ensuring adherence to Good Clinical Practice (GCP) guidelines.
Instrumental in elevating patient safety by introducing an improved Informed Consent process, resulting in a 20% increase in protocol compliance.
Transformed the Electronic Medical Record (EMR) system for efficient data collection which reduced input errors by 50%.
Developed a comprehensive onboarding program for new research staff which reduced the training period by 25%.
Leveraged my strong nursing background to provide acute care to patients participating in clinical trials, resulting in improved patient satisfaction by 35%. July 2014 - February 2019
Senior Clinical Research Nurse
Led a team in management of 20+ oncology clinical research projects, promoting the use of innovative methodologies
Leveraged strong leadership skills to manage a team of 4 research nurses, ensuring trials were conducted in compliance with protocol
Implemented a new protocol for inpatient care, improving patient satisfaction by 40%.
Mount Sinai Medical Center March 2008 - June 2014
Clinical Research Specialist
Spearheaded the development of 10+ clinical research initiatives, boosting patient safety measures by 20%
Implemented Good Clinical Practice (GCP) guidelines resulting in a 50% reduction in protocol deviations
Worked closely with medical teams to facilitate the understanding of research in practice, improving patient participation by 30%.
Resume Worded University May 2013
Master of Science in Nursing (MSN) - Clinical Research
Graduated Summa Cum Laude (Top 5%)
Resume Worded Academic Center April 2008
Certified Research Nurse (CRN) Course
Completed course during part-time while working at Mount Sinai Medical Center
Research Tools: Clinical Conductor CTMS, OpenClinica, Medidata Rave, iMedidata, SPSS, nQuery
Clinical Procedures: Patient Care, Vital Sign Checks, Phlebotomy, IV Insertion, ECGs
Regulatory Compliance: FDA guidelines, ICH-GCP standards, EMA guidelines, IRB submissions, Clinical trial protocols
Data Management: Electronic Data Capture (EDC), Data Quality Oversight, Solid Clinical Data Management
Certifications: Certified Oncology Nurse (OCN), Advanced Cardiovascular Life Support (ACLS) Certification
Awards & Recognition: ‘Nurse of The Year’,, 2017; ‘Exemplary Clinical Performance Award’, Mount Sinai Medical Center, 2012
Professional Memberships: Member, American Association of Critical-Care Nurses (AACN), Member, Society of Clinical Research Associates (SOCRA)
Volunteering: Volunteer Nurse, Medical Mission Trips to Kenya, 2018; Health Camp Volunteer, Local Community Center, 2019
Your Name
Oncology Clinical Research Nurse
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded July 2017 - Present
Oncology Clinical Research Nurse
Oversaw 15+ oncology clinical research projects in accordance with Good Clinical Practice (GCP), maintaining protocol compliance at over 95%
Adopted a hands-on approach in patient safety, leading to a 30% reduction in adverse events within a year
Revolutionized the Electronic Medical Record (EMR) system, expediting data retrieval by 40%
Organized and led education sessions on Oncology Research for 50+ nursing staff, increasing study enrollment by 15%
Streamlined the process for obtaining Informed Consent, leading to an increase in patient satisfaction by 20%. January 2011 - June 2017
Clinical Research Nurse
Managed 10+ clinical trials, enhancing adherence to protocols by 25%
Implemented healthcare management strategies that improved patient care during trials by 30%
Developed a new patient-oriented approach for Informed Consent, improving patient comprehension by 40%.
Cleveland Clinic February 2006 - December 2010
Clinical Research Assistant
Assisted in the planning and execution of 5 large-scale clinical trials, reducing data discrepancies by 20%
Leveraged healthcare information technology (HIT) to optimize data accuracy and reliability
Contributed to the development of protocols ensuring improved adherence to patient safety measures.
Resume Worded Institute December 2016
Certified Clinical Research Professional (CCRP)
Certification awarded in recognition of comprehensive understanding of clinical research processes and ethical standards
Resume Worded University May 2005
Bachelor of Science in Nursing (BSN)
Specialization in Oncology Nursing
Graduated Magna Cum Laude
Medical Skills: Phlebotomy, Electrocardiogram, Intravenous therapy, Pulmonary resuscitation, Pain management, Patient positioning
Technical Skills: Centricity Electronic Medical Records (EMR), SOS, ClinPlus, Microsoft Office Suite, SurgiNet, Medical coding (ICD-10)
Research Skills: Quantitative research, Patient Recruitment, Clinical trial management, Record Keeping, Data collection and aggregation, Protocol Adaptation
Languages: English (Native), Spanish (Professional Proficiency), French (Conversational)
Certifications: Oncology Nursing Certification (ONC) - Oncology Nursing Certificate Board, Advanced Cardiac Life Support (ACLS) - American Heart Association
Awards: Nurse of the Year 2016 -
Projects: Initiated a comprehensive clinical research study on the effectiveness of targeted therapy in breast cancer patients, resulting in a 20% increase in survival rate
Volunteering: Organizer of annual charity run event for cancer research - 2014 to Present
Your Name
Clinical Trials Nurse
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded August 2018 - Present
Clinical Trials Nurse
Administered 20+ clinical trials effectively implementing Good Clinical Practice (GCP) resulting in improved data integrity by 30%
Developed and delivered training materials on clinical trial procedures to 70+ staff members, enhancing overall team proficiency
Incorporated healthcare information technology (HIT) into data collection process, expediting the recording time by 20%
Played a key role in ensuring patient safety by implementing risk assessment strategies, drastically reducing adverse events by 30%
Implemented a new method for obtaining Informed Consent leading to improved patient comprehension and consent rates. April 2012 - July 2018
Clinical Trials Coordinator
Assisted in managing a portfolio of 15 clinical trials, enhancing the efficiency of operations by 25%
Played a pivotal role in streamlining the EMR system, reducing data input time by 20%
Improved patient safety by incorporating risk prevention initiatives resulting in 10% reduction of safety incidents.
Johns Hopkins Hospital September 2007 - March 2012
Clinical Research Associate
Contributed to the execution of 10+ clinical trials maintaining meticulous detail and adherence to protocols
Assisted in implementing new strategies for inpatient care resulting in increased patient satisfaction by 15%
Leveraged HIT in managing trial data, improving efficiency by 25%.
Resume Worded University June 2007
Masters of Science in Clinical Research
Topics: Clinical Investigation, Ethics and Clinical Research, Quantitative Techniques
Resume Worded Institute May 2003
Bachelors of Nursing
Awards: Dean's List 2002 (Top 10%)
Additional studies in pharmaceutical science
Clinical Research: Clinical Trial Protocols, Ethical Guidelines, Informed Consents, Protocol Developments, Statistic Applications, Data Analysis
Techniques: Phlebotomy, Intravenous Therapy, Wound Care, Patient Care, Medical Terminology, GCP Guidelines
Software Proficiency: MS Office Suite, SPSS, CTMS, EDC systems, EVRS software, Oracle Clinical
Certifications: Certified Clinical Research Professional, Association of Clinical Research Professionals (ACRP, 2019)
Leadership & Volunteering: Volunteer Clinical Staff, Johns Hopkins Community Outreach Program (2007-2012)
Publications: Co-authored a peer-reviewed journal publication about subjects' rights in clinical trials
Your Name
Clinical Research Consultant
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded January 2021 - Present
Senior Clinical Research Associate
Strategized and implemented an optimized Clinical Trial Management System (CTMS), reducing project timelines by 15%.
Oversaw clinical development of four therapeutic areas, enhancing efficiency in drug delivery by 30%.
Fostered a culture of Good Clinical Practice (GCP), resulting in a 10% rise in regulatory compliance.
Spearheaded the clinical operations for 7 key project portfolios, improving project success rate by 20%.
Managed U.S. Food and Drug Administration (FDA) regulatory submissions, achieving 100% acceptance rate for new drug applications. May 2018 - December 2020
Clinical Research Associate
Enhanced data quality by implementing Electronic Data Capture (EDC) protocol, reducing data errors by 25%.
Collaborated with CRO to manage clinical research for 3 oncology projects, leading to successful Phase II trials.
Contributed to designing Standard Operating Procedures (SOP), improving process efficiency by 18%.
Johnson & Johnson February 2015 - April 2018
Clinical Research Coordinator
Coordinated and monitored 15+ clinical trials successfully, meeting all project deadlines.
Handled regulatory affairs with a 100% compliance record.
Contributed to clinical data management, reducing data discrepancies by 20%.
Clinical Research Skills: Study Design, Statistical Analysis, Data Interpretation, Protocol Development, Regulatory Compliance
Technical Proficiency: MS Office Suite, SAS, STATA, Oracle Clinical, ClinTrial, ClinCapture, Medidata Rave
Pharmacovigilance Tools: Argus Safety, ARISg
Softwares: Electronic Data Capture (EDC), Trial Master File (TMF)
Certifications: Good Clinical Practice (GCP) Certificate - NIHR Clinical Research Network (2020)
Leadership & Volunteering: Volunteer, Doctors without Borders; Administered emergency medical care in remote areas of South America (2016-2017)
Courses: Complete Clinical Trials Management Course - Columbia University (2012)
Awards: Research Excellence Award, Resume Worded University (2011)
Your Name
Clinical Trial Manager
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE March 2021 - Present
Clinical Trial Manager
Increased trial efficiency by 22% through strategic implementation of Clinical Trial Management System (CTMS).
Enhanced patient safety by implementing strict adherence to Good Clinical Practice (GCP).
Successfully managed five global clinical trials in infectious diseases, leading to FDA approval of two novel drugs.
Reduced costs by 18% by optimizing clinical operations and forging strategic partnerships.
Oversaw FDA regulatory submissions leading to an impressive approval rate of 96%.
Resume Worded August 2016 - February 2021
Senior Clinical Research Associate
Managed the clinical development of three innovative drug programs from concept to Phase III trials.
Implemented Electronic Data Capture (EDC) protocol, leading to a reduction in time and resources consuming manual data entry by 30%.
Facilitated training sessions on Standard Operating Procedures (SOP), enhancing team's protocol compliance by 20%.
Pfizer April 2013 - July 2016
Clinical Research Coordinator
Coordinated a series of oncology clinical trials, leading to the completion of Phase I and II within stipulated timelines.
Contributed to successful FDA regulatory submission for an oncology drug, leading to Phase III trials.
Worked on clinical data management, improving data accuracy by 25%.
Resume Worded Academic Center August 2016
Master in Clinical Research
Concentration in Regulatory Affairs
Resume Worded University April 2013
Bachelor of Science in Biology
Minor in Bioinformatics
Graduated Magna cum Laude
Clinical Research: Clinical Trial Design, Protocol Development, Regulated Document Management
Software and Tools: eTMF Systems, Microsoft Office (Word, Excel, PowerPoint), Clinical Trial Management Systems (CTMS)
Regulation and Compliance: ICH-GCP, FDA Regulations, EMA Guidelines
Medical Writing: Clinical Study Report (CSR) Writing, Informed Consent Forms, Patient Information Sheets
Certifications: Certified Clinical Research Professionals (CCRP)
Leadership & Volunteering: Founding Member of Clinical Research Professionals Network, Community Health Volunteer at Local Health Clinic
Awards: National Award for Excellence in Clinical Trial Design (2020), Orion Award for Innovative Thinking (2019)
Continuing Education: Attended Clinical Research Training Course - Harvard Medical School
Your Name
Clinical Operations Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded June 2020 - Present
Clinical Operations Manager
Structured and led a cross-functional team to manage clinical operations, reducing operational bottlenecks by 20%.
Successfully coordinated and completed three clinical trial projects within deadlines under strict adherence to Good Clinical Practice (GCP).
Spearheaded the implementation of Clinical Trial Management System (CTMS), resulting in a 25% increase in project efficiency.
Orchestrated U.S. Food and Drug Administration (FDA) regulatory submissions, achieving a 98% acceptance rate.
Implemented an Electronic Data Capture (EDC) protocol which resulted in a 18% reduction in erroneous data. January 2017 - May 2020
Clinical Trial Manager
Managed and coordinated clinical trials in three therapeutic areas, achieving 100% completion rate under budget.
Improved the process efficiency by 15% by designing and implementing Standard Operating Procedure (SOP).
Leveraged biotechnology innovations to drive clinical research, resulting in progress of two novel drugs to Phase II trials.
Novartis March 2014 - December 2016
Senior Clinical Research Associate
Initiated and completed two clinical research projects, paving way for crucial Phase II clinical trials.
Ensured 100% compliance with regulatory affairs, thus maintaining an exceptional audit record.
Managed clinical data to ensure accuracy and integrity, reducing data discrepancies by 17%.
Resume Worded Academic Center June 2015
Master's Degree in Clinical Research Administration
Specialized in Clinical Trials Management
Resume Worded University April 2011
Bachelor of Science in Life Sciences
Minors in Health Care Administration and Management
Dean's List 2010 (Top 10%)
Clinical Operations Management: Trial Protocol Development, Clinical Trial Management, Clinical Project Oversight, Regulatory Compliance, Patient Recruitment, Contract Negotiation
Software & IT: Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), Microsoft Office Suite
Languages: English (Native), Spanish (Fluent), French (Conversational)
Research Tools: MEDLINE,, PubMed, EMBASE
Certifications: Certified Clinical Research Associate (CCRA), Society for Clinical Research Sites (SCRS) Leadership Certification (2019)
Awards: Outstanding Leadership Award, (2019),Novartis Research Excellence Award (2016)
Leadership & Volunteering: American Association of Clinical Research Professionals (Board Member), Resume Worded Community Volunteer Program (Volunteer)
Professional Development: Attended yearly industry conferences including International Conference on Clinical Trials, Clinical Operations in Oncology Trials West Coast, and Global Forum on Bioethics in Research

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

Review the job posting closely.

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

Add industry skills like Protocol and Informed Consent.

Add other common skills from your industry - such as Institutional Review Board (IRB), Electronic Data Capture (EDC) and Oncology Clinical Research - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like Regulatory Submissions, Patient Recruitment 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, Clinical Research 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 Clinical Research 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, Clinical Research Coordinator, somewhere into your resume to get past resume screeners. See the infographic for how to do this.

Word Cloud for Clinical Research Coordinator Skills & Keywords

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

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Clinical Research 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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Policy and Research Policy Analyst

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Browse Skills from Similar Jobs

Frequently Asked Questions

What skills do hiring managers want to see on a Clinical Research Coordinator resume?

The most common skills and keywords we found on Clinical Research Coordinator resumes and job postings were Good Clinical Practice (GCP), Clinical Research, Clinical Trials, Institutional Review Board (IRB), Electronic Data Capture (EDC), Informed Consent, Protocol and Oncology Clinical Research.

Skills like Patient Recruitment, Phlebotomy, Regulatory Submissions, Study Coordination and Data Analysis also appeared on related job postings.

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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