Clinical Trial Manager

Clinical Trial Manager Resume Keywords and Skills (Hard Skills)

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

  •   Show full list

Resume Skills: Research

  • Designing and Conducting Clinical Trials
  • Regulatory Compliance
  • Patient Recruitment
  • Data Analysis
  • Site Monitoring
  • Report Writing
  • Quality assurance
  • Experimental design
  • Regulatory submission
  • Data Management
  • Oracle Clinical
  • Clinical Trial Design
  • Protocol Development
  • Regulated Document Management
  • Clinical Trial Monitoring
  • Ethics in Clinical Research
  • Clinical Data Management
  • Clinical Trial Designs
  • Site Management
  • Trial Monitoring
  • Statistical Application
  • Medidata
  • ClinCapture
  • REDCap
  • OpenClinica
  • Clinical Conductor
  • MasterControl
  • CTMS
  • CDMS
  • EDC
  • Medidata Rave
  • SAS
  •  Match your resume to these skills

Resume Skills: Regulatory Compliance

  • FDA/ICH Guidelines
  • Good Clinical Practice (GCP)
  • Ethical Code Compliance
  • Adverse Event Reporting
  • FDA Regulations
  • ICH Guidelines
  • GCP Guidelines
  • Patient Confidentiality (HIPAA)
  • Drug Development Process
  • EMA Guidelines
  • FDA Regulatory Guidelines
  • Quality Assurance
  • Good Clinical Practices
  • ICMJE Recommendations
  •  Match your resume to these skills

Resume Skills: Software Proficiency

Resume Skills: Technologies and Tools

Resume Skills: Languages

Resume Skills: Technical

Resume Skills: Project Management

  • Resource planning
  • Risk management
  • Stakeholder management
  • Budgeting
  • Timelines and schedules
  • Gantt charts
  • Risk Management
  • Stakeholder Management
  • Resource Allocation
  • Quality Assurance
  • Conflict Resolution
  • MS Project
  • Quality Management
  •  Match your resume to these skills

Resume Skills: Medical Knowledge

Resume Skills: Software and Tools

Resume Skills: Medical Writing

Resume Skills: Data Management

Resume Skills: Communication & Documentation

Resume Skills: Clinical Regulatory Standards

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 Trial 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 Trial 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.

Select a free resume example
Your Name
Clinical Trial Manager
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded June 2019 - Present
Senior Clinical Trial Manager
Innovated a streamlined approach to data collection through Electronic Data Capture (EDC), resulting in a 30% reduction in data errors and a 20% decrease in collection times.
Led a diversified team to carry out multiple oncology-based clinical trials, resulting in the successful development and FDA approval of two new cancer drugs.
Implemented SOPs based on Good Clinical Practice (GCP) guidelines, leading to zero non-compliance during a US FDA audit.
Leveraged the Clinical Trial Management System (CTMS) to effectively manage resources, milestones and budgets for 7 concurrent clinical trials.
Conducted regular Clinical Monitoring to ensure data integrity, patient safety, and adherence to protocol, securing 100% regulatory compliance across all trials.
Roche Pharmaceuticals January 2017 - May 2019
Clinical Trial Manager
Propelled drug development programs by designing clinical trial protocols and coordinating 3 global trials, leading to 2 promising therapeutic products.
Achieved 15% reduction in trial costs via proactive CRO management, consistent budget monitoring, and negotiation of service agreements.
Facilitated FDA regulatory submissions, leading to timely green signal for 4 drug developments.
Coordinated Biotechnology trials, resulting in a pipeline of 5 potential life-saving treatments.
Optimized Clinical Data Management processes, enhancing data accuracy by 25%.
Eli Lilly and Company September 2015 - December 2016
Clinical Research Associate
Catalyzed clinical trial efficiency through robust trial management, driving a 20% improvement in trial completion rates.
Played a pivotal role in clinical development programs, facilitating the creation of 3 innovative drug solutions.
Enhanced protocol adherence through stringent monitoring, recording a 100% rate in compliance across all assigned tasks.
Resume Worded University June 2015
Master of Science in Clinical Research
Specialized in clinical trial management techniques and methodologies
Resume Worded Academic Center May 2013
Certified Clinical Research Professional (CCRP)
Acquired skills in trial design & implementation, regulatory compliance, data management and research ethics
Clinical Research: Quality assurance, Experimental design, Regulatory submission, Data Management, SANOFI CTMS, Oracle Clinical
Project Management: Resource planning, Risk management, Stakeholder management, Budgeting, Timelines and schedules, Gantt charts
Medical Knowledge: Medical terminology, Pharmacovigilance, Drug development process, GCP (Good Clinical Practice), ICH guidelines, EDC (Electronic Data Capture)
Software Proficiency: Microsoft Office Suite, SPSS Statistics, Medidata Rave, ClinPlus, eTMF, JMP Clinical
Certifications: Certified Project Management Professional (PMP) - PMI, Certified in Public Health (CPH) - NBPHE
Vocational Training: Advanced Training in Clinical Pharmacology - Resume Worded Academic Center
Volunteering: American Association of Cancer Research - Volunteer Clinical Research Coordinator (2015-2016)
Professional Memberships: Member of the Association of Clinical Research Professionals (ACRP), Member of the Society of Clinical Trials (SCT)
Your Name
Clinical Trial Coordinator
City, Country  •  (123) 456-789  •  [email protected]  •
EXPERIENCE April 2018 - Present
Clinical Trial Manager
Implemented a Clinical Trial Management System (CTMS), optimizing operational efficiency by 40%.
Directed a clinical development team to fast-track an oncology drug, securing FDA approval 6 months ahead of schedule.
Led protocol development for 4 clinical trials within the biotechnology and therapeutic areas, resulting in the identification of 3 new treatment methods.
Strengthened regulatory affairs procedure, leading to an 18% increase in speed of Regulatory submissions and approvals.
Managed CROs globally, leading to efficient data capture, quality control measures, and sustainable reduction in trial overhead costs by 17%.
Amgen Inc September 2015 - March 2018
Clinical Trial Coordinator
Executed clinical operations flawlessly, accelerating 3 drug development phases.
Ensured GCP compliance on all projects, maintaining a 100% audit success rate.
Played a vital role in implementing a new EDC system, reducing data management errors by 25%.
Resume Worded University 2015
Master of Science in Clinical Research Administration
Specialization in Clinical Trials Management and Regulatory Compliance
Resume Worded Institute 2014
Certified Clinical Research Professional (CCRP)
Maintained CCRP certification via continuous education and training
Clinical Trial Management Softwares: Medidata, Oracle Clinical, ClinCapture, REDCap, OpenClinica, Clinical Conductor, MasterControl
Regulatory Compliance: FDA Regulations, ICH Guidelines, GCP Guidelines, Patient Confidentiality (HIPAA), Drug Development Process
Project Management: Risk Management, Stakeholder Management, Resource Allocation, Quality Assurance, Conflict Resolution
Data Management: Data Quality Control, Data Validation, Data Cleaning, Clinical Data Reporting, Electronic Data Capture (EDC)
Certifications: Project Management Professional (PMP) - Project Management Institute (PMI)
Awards: ‘Outstanding Clinical Researcher’ – Resume Worded Annual Award (2016)
Professional Membership: Member, Society of Clinical Research Associates
Publications: Co-author, 'Transparency and Reproducibility in Clinical Trials: Progress and Prospects' – Health Affairs Journal
Your Name
Clinical Research Associate
City, Country  •  (123) 456-789  •  [email protected]  •
Resume Worded October 2017 - Present
Clinical Trial Manager
Led the Clinical Monitoring team to implement GCP principles, ensuring data accuracy and patient safety across all 5 ongoing trials, with zero protocol deviations.
Expedited two novel therapeutic solutions for clinical trials, contributing significantly to organisational portfolio.
Optimized Clinical Operations by implementing a robust CTMS, leading to a 30% increase in trial efficiency.
Integrated the use of an EDC system, resulting in a 20% faster data collection process.
Reduced study budget by 25% by effectively negotiating contracts and managing CRO resources.
Novartis August 2015 - September 2017
Senior Clinical Research Associate
Streamlined Clinical Data Management procedures, leading to a 22% improvement in the data processing speed.
Implemented strict SOPs across all trials, maintaining 100% compliance with FDA regulations.
Assisted in trial protocol drafting in accordance with FDA guidelines, contributing to rapid progression of 3 drugs into clinical trials.
Resume Worded University May 2015
Master of Health Science - Clinical Research
Specialization in Biostatistics and Study Designs
Resume Worded Academic Center January 2013
Certified Clinical Research Associate
Obtained knowledge of Guidelines & Regulations, Data Management and Quality Assurance
Clinical Research Skills: Clinical Trial Monitoring, Ethics in Clinical Research, Clinical Data Management, Clinical Trial Designs, Regulatory Compliance, Patient Recruitment
Biostatistics Software: SPSS, SAS, R, Stata, Prism, Seagull
Communication & Documentation: Medical Reporting, Protocol Writing, Patient informed Consent forms, Medical Review, Medical Documentation
Regulatory & Quality Assurance: FDA Regulatory Guidelines, Quality Assurance, Good Clinical Practices, ICMJE Recommendations, EMA Guidelines
Certifications: Certified Good Clinical Practice (GCP) Professional, Clinical Trial Manager Certification (CTM)
Leadership & Volunteering: Volunteer Clinical Researcher for The Cancer Research Non-profit, Mentor for Emerging Clinical Researchers
Professional Organizations: Member of Association of Clinical Research Professionals (ACRP), Society of Clinical Trials (SCT)
Projects: Implemented advanced recruitment tactics for clinical trial, leading to 50% increase in trial participants
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 Trial Manager resume?

Review the job posting closely.

Go through the Clinical Trial Manager posting you're applying to, and identify hard skills the company is looking for. For example, skills like Clinical Monitoring, Clinical Trial Management System (CTMS) and Clinical Trials are possible skills. These are skills you should try to include on your resume.

Add industry skills like Clinical Operations and Clinical Development.

Add other common skills from your industry - such as Good Clinical Practice (GCP), CRO Management and Electronic Data Capture (EDC) - into your resume if they're relevant.

Add skills into your work experience.

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

Show examples of where you trained people.

On Clinical Trial Manager resumes, you should give specific accomplishments that involve you training others, whether that's in your team or other stakeholders.

Highlight leadership and management skills.

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

Use the exact job title.

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

Word Cloud for Clinical Trial Manager Skills & Keywords

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

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Clinical Trial 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
Clinical Trial Manager

Resume Example

Resume Example
Highlights (Free)

Resume Example
Modern Two-Column

Resume Example
Clean Modern

Resume Example
Entry-Level (Free)

Browse Skills from Similar Jobs

Frequently Asked Questions

What skills do hiring managers want to see on a Clinical Trial Manager resume?

Some effective Clinical Trial Manager skills you can add to your resume include:

  • Good Clinical Practice (GCP)
  • Clinical Trial Management System (CTMS)
  • Clinical Trials
  • Electronic Data Capture (EDC)
  • CRO Management
  • Clinical Development
  • Clinical Monitoring
  • Clinical Operations

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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