Clinical Research Project Manager

Clinical Research Project Manager Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Clinical Research Project Manager 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 Research
  • Institutional Review Board (IRB)
  • Protocol Development
  • Electronic Data Capture (EDC)
  • Clinical Trial Management System (CTMS)
  •  Find out what your resume's missing
  • Clinical Monitoring
  • Oncology
  • Protocol
  • Clinical Development
  • Regulatory Affairs
  • Life Sciences
  • Standard Operating Procedure (SOP)
  • Healthcare
  • Data Management
  • U.S. Food and Drug Administration (FDA)
  • Public Health
  • Data Collection
  • Biotechnology

  •   Show full list

Resume Skills: Clinical Research

Resume Skills: Administration & Policy Compliance

  • FDA Regulatory Requirements
  • Good Clinical Practices (GCP)
  • Standard Operating Procedures (SOPs)
  • Quality Assurance
  • Data Management
  • Safety Reporting
  •  Match your resume to these skills

Resume Skills: Project Management

Resume Skills: Software Proficiency

  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 Project Manager 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 Project Manager 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 Project Manager
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE May 2019 - Present
Clinical Research Project Manager
Spearheaded the development of 5 large-scale clinical research projects, utilizing Good Clinical Practice standards, leading to accurate and timely project completion
Implemented an efficient Clinical Trial Management System, reducing data management time by 30%
Achieved 100% protocol adherence in all projects through the meticulous supervision of clinical trials
Enhanced data collection procedures, leading to an improvement in data reliability by 50%
Established strong relationships with Regulatory Affairs, ensuring adherence to FDA guidelines and boosting project approval speed by 40%
Resume Worded February 2016 - April 2019
Clinical Research Associate
Improved the efficiency of the electronic data capture process by 20% through the implementation of a revamped Standard Operating Procedure
Oversaw data management for 15+ clinical trials, adhering to Good Clinical Practice (GCP) and ensuring 100% accuracy
Managed relationships with Institutional Review Boards, reducing review times by 25%.
Johnson & Johnson September 2012 - January 2016
Clinical Research Assistant
Assured strict protocol adherence in 10+ projects, leveraging understanding of Good Clinical Practice
Contributed to the development of clinical monitoring strategies, increasing team efficiency by 10%.
Resume Worded University May 2014
Master's in Clinical Research
Emphasis on Project Management, Processes & Protocols
Resume Worded Institute May 2012
Bachelor of Science in Nursing (BSN)
Minors in Health Administration
Dean's List 2010 - 2012 (Top 10%)
Clinical Research: Onsite Monitoring, Centralized Monitoring, Data Management
Project Management: Risk Management, Stakeholder Management, Resource Management, Scope Management
Software & Tools: Medidata Rave, Oracle Clinical, ClinCapture, REDCap, Microsoft Project
Regulations & Standards: ICH-GCP, FDA, EMA, MHRA, CDSCO, Health Canada
Certifications: Certified Clinical Research Professional (CCRP), Certified Project Management Professional (PMP)
Leadership & Volunteering: Medicine Sans Frontiers – Volunteer Clinical Researcher (2013-2015)
Projects: Implementation of a centralized monitoring system for XYZ study at
Your Name
Senior Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
Pfizer Inc. March 2020 - Present
Senior Clinical Research Coordinator
Orchestrated regulatory affairs for 25+ clinical trials, ensuring research protocols are as per FDA regulations, reducing non-compliance by 30%
Implemented comprehensive data management procedures, optimizing the electronic data capture process and reducing errors by 20%
Coordinated with researchers and health professionals, fostering interdepartmental collaboration and advancing 3 major Oncology projects.
Resume Worded May 2016 – February 2020
Clinical Research Coordinator
Led successful execution of 10 clinical trials, maintained 100% adherence to the protocol
Streamlined data collection processes, improving data accuracy by 30%
Facilitated strong rapport with the Institutional Review Board, expediting protocol approvals.
Pfizer Inc. January 2013 - April 2016
Clinical Research Associate
Assured adherence to Clinical Trial Management System protocols in 15+ projects
Contributed to the development of robust clinical monitoring strategies, leading to increased project efficiency.
Resume Worded Academic Center December 2018
Master of Science in Clinical Research
Dissertation on 'Accelerating Clinical Trials: Opportunities and Challenges'
Resume Worded University June 2012
Bachelor of Science - Biomedical Science
Minors in Data Analysis and Pharmaceutical Science
Awards: Dean's List 2010 and 2011 (Top 5%)
Clinical Research Tools: Medidata Rave, Oracle InForm, Clinical Conductor, ClinCapture, REDCap
Statistical and Data Analysis Software: SPSS, SAS, Stata, R
Regulatory Understanding: Good Clinical Practice (GCP), FDA Regulations, Clinical Trials Directives, ICH Guidelines
Project Management Tools: Smartsheet, Trello, MS Project, Asana, JIRA
Certifications: Certification in Clinical Data Management (2020), Registered Clinical Research Coordinator (RCRC) Certification (2016)
Projects: Designed and implemented successful phase 3 trial for groundbreaking diabetes drug (2020-2021)
Volunteering: Provided pro-bono consulting for local health specialists, helping to streamline patient data collection and analysis (2016 - Present)
Publications: Co-authored 'Streamlining Clinical Trials: A Methodological Approach' in The Clinical Research Journal (2019)
Your Name
Clinical Research Supervisor
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE June 2020 - Present
Clinical Research Supervisor
Oversaw a team of 10+ researchers undertaking various clinical projects, ensuring project completion within stipulated deadlines
Enhanced clinical trial monitoring procedures, resulting in a 20% increase in project efficiency
Liaised with FDA officials, ensuring clinical research protocols maintain 100% adherence to regulatory guidelines.
Streamlined data management procedures, boosting efficiency of Electronic Data Capture by 15%
Fostered a collaborative framework with Regulatory Affairs, resulting in quicker protocol development and approval processes.
Resume Worded August 2015 – May 2020
Clinical Research Project Manager
Managed large-scale clinical research projects, using Good Clinical Practice, ensuring timely and accurate completion
Implemented Clinical Trial Management System, leading to optimized data management
Boosted protocol adherence in all projects through strategic supervision.
Gilead Sciences January 2011 - July 2015
Clinical Research Associate
Maintained strict protocol adherence in 12+ projects, leveraging understanding of Good Clinical Practice
Contributed to the development of clinical monitoring strategies, boosting team efficiency by 15%.
Resume Worded University April 2015
Master of Science - Clinical Research Management
Concentration: Clinical trial management and oversight
Resume Worded Institute May 2010
Bachelor of Science - Biomedical Sciences
Minor in Clinical Trial Design
Awards: Dean's List 2007-2010
Clinical Research: Data Management, Protocol Development, Regulatory Compliance, Clinical Trials, Quality Management, Patient Recruitment
Software: Medidata Rave, CTMS, Oracle Clinical, Microsoft Office (Word, Excel, PowerPoint)
Regulatory Standards: ICH Guidelines, FDA regulations, GCP compliance, Quality Assurance
Laboratory Techniques: PCR, Cell Culture, Western Blotting, ELISA, Flow Cytometry, Microscopy
Certifications: Certified Clinical Research Coordinator (CCRC) - ACRP, 2014
Volunteering: Clinical Supervisor for Medical Camp, Resume Worded Foundation (2017-present), Volunteer at the City Animal Shelter (2019-present)
Projects: Established a database for the tracking of participant recruitment and patient data (2018)
Courses: Completed Advanced Course in Data Management and Statistics for Clinical Trials, 2019

How do I add skills to a Clinical Research Project Manager resume?

Review the job posting closely.

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

Add industry skills like Protocol Development and Institutional Review Board (IRB).

Add other common skills from your industry - such as Clinical Trial Management System (CTMS), Electronic Data Capture (EDC) and Clinical Trials - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like Data Management, Oncology and U.S. Food and Drug Administration (FDA) - into your work experience too. This shows hiring managers that you have practical experience with these tools, techniques and skills.

Highlight leadership and management skills.

Hiring managers often want to see evidence of leadership and management on a Clinical Research Project Manager resume, so try to include any examples of where you led a project or managed other people.

Show evidence of managing projects.

Leading and delivering projects to completion are critical skill sets when it comes to Clinical Research Project Manager roles.

Use the exact job title.

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

Word Cloud for Clinical Research Project Manager Skills & Keywords

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

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Clinical Research Project Manager 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 Clinical Research Project Manager resume?

The most common skills and keywords we found on Clinical Research Project Manager resumes and job postings were Clinical Trials, Good Clinical Practice (GCP), Clinical Research, Institutional Review Board (IRB), Protocol Development, Electronic Data Capture (EDC), Clinical Trial Management System (CTMS) and Clinical Monitoring.

Skills like Clinical Development, U.S. Food and Drug Administration (FDA), Data Collection, Data Management and Oncology 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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