Clinical Project Manager

Clinical Project Manager Resume Keywords and Skills (Hard Skills)

Here are the keywords and skills that appear most frequently on recent Clinical 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
  • Good Clinical Practice (GCP)
  • Clinical Trials
  • CRO Management
  • Clinical Development
  • Clinical Trial Management System (CTMS)
  • Electronic Data Capture (EDC)
  • Clinical Research
  •  Find out what your resume's missing
  • Clinical Monitoring
  • Standard Operating Procedure (SOP)
  • Biotechnology
  • Oncology
  • Protocol
  • Clinical Operations
  • Clinical Data Management
  • U.S. Food and Drug Administration (FDA)
  • Drug Development
  • Trial Management
  • Life Sciences
  • Therapeutic Areas
  • Regulatory Submissions

  •   Show full list

Resume Skills: Software

  • MS Project
  • MS Office
  • Clinical Trial Management Systems (CTMS)
  • Oracle Clinical
  • SAS
  • Microsoft Project
  • Medidata
  • CTMS (Clinical Trial Management System)
  • Microsoft Office Suite
  • Electronic Medical Records
  • Statistical Analysis Software (SAS)
  • LiquidPlanner
  • Smartsheet
  • Basecamp
  • Medidata Rave
  • EDC
  • IVRS
  •  Match your resume to these skills

Resume Skills: Technical

Resume Skills: Analytical Tools

Resume Skills: Medical Proficiencies

Resume Skills: Language

Resume Skills: Clinical Research

  • Patient Recruitment
  • Data Collection
  • Compliance & Ethics
  • CRO Management
  • Sites Monitoring
  • Clinical Data Review
  • Safety Management
  • Study Protocols
  • ICH-GCP (International Council for Harmonisation - Good Clinical Practice)
  • Clinical Trials
  • Data Analysis
  • Patient Screening
  • Medical Writing
  • Report Generation
  •  Match your resume to these skills

Resume Skills: Project Management

  • Risk Analysis
  • Project Scheduling
  • Resource Allocation
  • Planning & Budgeting
  • Risk Assessment & Mitigation
  • Team Leadership
  • Scheduling & Timelines
  • Budgeting
  • Planning
  • Monitoring
  • Reporting
  •  Match your resume to these skills

Resume Skills: Data Management

Resume Skills: Regulations & Standards

Resume Skills: Regulatory Compliance

Resume Skills: Regulations Knowledge

Resume Skills: Data Analysis Tools

Resume Skills: Quality Assurance

Resume Skills: Program Management

Resume Skills: Certifications

  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 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 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 Project Manager
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE January 2022 - Present
Senior Clinical Project Manager
Ensured compliance to Good Clinical Practice (GCP) and Regulatory Submissions by introducing exhaustive Standard Operating Procedure (SOP) checks, improving overall compliance by 35%
Managed a large-scale Oncology project efficiently, reducing overall costs by 20% while maintaining quality and timeline adherence
Leveraged Clinical Trial Management System (CTMS) to increase team productivity, leading to a 15% reduction in time taken per project
Incorporated the use of Electronic Data Capture (EDC) to improve data accuracy and optimize clinical operations
Streamlined Clinical Development by effectively training and monitoring 10+ Clinical Research staff, improving project delivery rates by 25%
Resume Worded June 2017 - December 2021
Clinical Project Manager
Led a biotechnology project team of 6 and successfully delivered projects 3 months ahead of schedule
Implemented Clinical Trials management strategies, leading to 30% improvement in project execution and efficiency
Designed and supervised Clinical Trial Protocol alignment, reducing discrepancies by 45%
Novartis May 2013 - June 2017
Assistant Clinical Project Manager
Managed Trial Management for 3 drugs, ensuring compliances and meeting FDA guidelines
Assisted in Clinical Data Management, significantly reducing data errors by around 28%
Contributed significantly to the identification and engagement of therapeutic areas appropriate for study
Resume Worded University April 2022
Master's in Clinical Research Administration
Specialized coursework in clinical project management, clinical trial regulations, and medical product development
Resume Worded Institute May 2013
Bachelor of Science in Biology
Minors in Mathematics and Statistics
Awards: Resume Worded Teaching Fellow (only awarded to top 5%), Dean's List 2012 (Top 10%)
Project Management Software: MS Project, LiquidPlanner, Smartsheet, Basecamp
Clinical Software: Medidata Rave, EDC, Oracle Clinical, IVRS
Regulations Knowledge: ICH Guidelines, GCP, FDA regulations, EMA regulations
Data Analysis Tools: SPSS, Stata, SAS, Tableau
Certifications: Project Management Professional (PMP, 2022), Certified Clinical Research Professional (CCRP, 2018)
Leadership & Volunteering: Clinical Research Network (Board Member and Chair), Mentored new clinical project managers with Clinical Project Management Association (2018-Present)
Projects: Spearheaded the 'MedicalHeroes' project - an awareness campaign aimed at advocating for clinical trial participants (2017)
Awards: Awarded the 'Innovation in Clinical Research' prize by the Clinical Research Association, 2021
Your Name
Clinical Research Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE August 2021 - Present
Clinical Research Coordinator
Coordinated life sciences studies for 5+ different projects, increasing study completion rates by 20%
Managed CRO operations efficiently, reducing study time by 15% and saving more than $100K in research costs
Conducted meticulous Clinical Monitoring, reducing data discrepancies by over 40% and improving research accuracy
Developed detailed clinical research protocols to optimize trials and improved standardization across the department by 30%
Utilized the Clinical Trial Management System (CTMS) to manage project resources, increasing efficiency by 25%
Resume Worded February 2015 - July 2021
Clinical Trials Associate
Managed 15+ clinical trials, maintaining 98% accuracy and adherence to FDA guidelines
Implemented electronic data capture systems, reducing data loss by 35% and improving overall data integrity
Contributed to the drug development process, resulting in 2 approved drugs in the Oncology therapeutic area
Pfizer April 2010 - January 2015
Research Associate
Assisted in the coordination of clinical operations for 3 key projects, contributing to a 10% increase in operational efficiency
Compiled and managed accurate clinical data, aiding in the successful completion of multiple projects
Resume Worded Academic Center May 2010
Master's Degree in Clinical Research
Focused coursework on Clinical Trials, Epidemiology, Biostatistics, and Ethical and Legal issues
Resume Worded University May 2008
Bachelor of Science in Biology
Specialized in Molecular Biology and Biochemistry
Recipient of Scientific Excellence Award
Technical Skills: Clinical data management systems (CDMS), Familiar with FDA regulations, Proficient in Phase I - IV trials, Epidata, OpenClinica, ClinCapture
Analytical Tools: SPSS, SAS, DATAV, MS Excel, R (Statistical Computing Software), Python(Basic)
Medical Proficiencies: Clinical Pharmacology, Clinical Immunology, Informed Consent Processes, Patient Recruitment Strategies, Protocol Development
Language: English (Native), Spanish (Conversational), French (Basic)
Certifications: Certified Clinical Research Coordinator(CCRC) - Association of Clinical Research Professionals (ACRP)
Courses and Trainings: Good Clinical Practice (GCP) Course - International Council for Harmonisation (ICH), Clinical Research Ethics Training - Resume Worded
Leadership & Volunteering: Volunteer - Health Awareness Campaigns (2014), Mission Trip Medical Aid - Guatemala (2016)
Awards & Accomplishments: Best Clinical Research Coordinator of the Year - (2022), Pfizer Innovation Excellence Award (2014)
Your Name
Clinical Program Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded September 2020 - Present
Clinical Program Manager
Drove the clinical development strategy for 4 key programs leading to faster FDA approvals
Implemented a new CTMS system resulting in a 20% improvement in data management accuracy and streamlining workflow across the Clinical Operations department
Managed and mentored a team of 15 Clinical Research Associates, improved overall team performance by 35%
Spearheaded cross-functional coordination between the Clinical Monitoring and Clinical Data Management teams, leading to a 10% reduction in project duration
Proactively managed CRO relationships, resulting in cost savings of $500K annually April 2014 - August 2020
Clinical Project Manager
Managed 5+ parallel clinical projects leveraging efficient resource allocation, leading to a 20% reduction in project costs
Empowered the team with robust understanding of GCP norms, resulting in zero non-compliance issues over a 3-year period
Transformed the Clinical Trials process by integrating EDC, enhancing data accuracy by 25%
Merck September 2009 - March 2014
Clinical Research Associate
Streamlined data monitoring processes, reducing data discrepancies by around 35%
Played a key role in protocol design, contributing to successful FDA approval of 2 drugs
Resume Worded University August 2009
Master of Science in Clinical Research
Concentration in Clinical Trials Management
Resume Worded Academic Center May 2007
Bachelor of Science in Biochemistry
Minors in Business Administration
Awards: Resume Worded Academic Excellence (Top 10% of the class)
Program Management: Project Planning, Leadership and Supervision, Risk Management, Regulatory Compliance, Budgeting and Finance, Lean Six Sigma
Clinical Research: Clinical Trials, Data Analysis, Patient Screening, Data Collection, Medical Writing, Report Generation
Software: Microsoft Office Suite (Advanced), Electronic Medical Records (Proficient), Statistical Analysis Software (SAS)(Intermediate)
Certifications: Certified Clinical Project Manager (CCPM), Certified Clinical Research Associate (CCRA), Certified Project Management Professional (PMP)
Certifications: Certified Clinical Research Coordinator (CCRC) (2018 - Present), Certified Six Sigma Blackbelt (CSSBB) (2017 - Present)
Leadership & Volunteering: American Cancer Society (Event Organizer and Volunteer, 2010 - Present), American Association of Clinical Research Professionals (Member, 2009 - Present)
Publications & Projects: Co-Author of 'Modern Approaches to Clinical Trials: Optimization Strategies' (2015), Project Lead for 'Nanotech in Oncology Study' (2016 - 2018)
Professional Development: Attended Clinical Operations Strategy Meeting 2019, Completed Continuing Education in Clinical Research (Yearly)

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

Review the job posting closely.

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

Add industry skills like CRO Management and Clinical Trials.

Add other common skills from your industry - such as Clinical Trial Management System (CTMS), Good Clinical Practice (GCP) and Clinical Monitoring - into your resume if they're relevant.

Add skills into your work experience.

Incorporate skills - like Oncology, Drug Development and Standard Operating Procedure (SOP) - 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 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 Project Manager roles.

Use the exact job title.

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

Word Cloud for Clinical Project Manager Skills & Keywords

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

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Clinical 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.

Resume Example
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Resume Example
Senior Project Manager

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Technical Project Manager

Resume Example
Marketing Project Manager

Resume Example
IT Project Coordinator

Resume Example
Construction Project Coordinator

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Frequently Asked Questions

What hard skills should you include on a Clinical Project Manager resume?

Some popular Clinical Project Manager hard skills are Good Clinical Practice (GCP), Clinical Trials, CRO Management, Clinical Development, Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), Clinical Research and Clinical Monitoring.

Depending on the job you apply to, skills like Oncology, Trial Management, Therapeutic Areas, Drug Development and Standard Operating Procedure (SOP) can also be good 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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