Clinical Trial Associate

Writing a great clinical trial associate resume is important because it is one of the first things a potential employer will see when they are considering you for a position. It is your opportunity to make a good first impression and sell yourself as the best candidate for the job.

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If you're looking for inspiration when it comes to drafting your own clinical trial associate resume, look no further than the samples below. These resumes will help you highlight your experience and qualifications in the most effective way possible, giving you the best chance of landing the clinical trial associate job you're after.

Resume samples

Kinsleigh Lanouette

kinsleigh.lanouette@gmail.com | (404) 594-1735 | 5678 Sunset Blvd, Seattle, WA 98116

Summary


I am a Clinical Trial Associate with over 1 year of experience in the industry. I have worked on various clinical trials and have gained valuable knowledge and skillsets during my time. I am extremely organized and detail-oriented, which has allowed me to excel in this field. I possess excellent communication abilities, both written and verbal, which are crucial in this line of work. My interpersonal skills allow me to build positive relationships with patients, families, staff members, and other important stakeholders involved in clinical trials. Overall, I am a highly capable individual who is able to effectively contribute to the success of any clinical trial project

Experience


Clinical Trial Associate at PRA Health Sciences, WAMar 2022 - Present

  • Led the clinical trial for a new medication with 100 participants, overseeing all aspects of the study from start to finish.
  • Successfully recruited and enrolled patients into clinical trials.
  • Monitors patient progress during clinical trials and reports any adverse reactions or events.
  • Maintains accurate and up-to-date regulatory documentation throughout the duration of the trial.
  • Tracks milestones and deadlines for each phase of the trial ensuring that they are met according to protocol.
  • Conducts quality control checks on data collected during clinical trials.

Clinical Trial Associate I at ICON Clinical Research, WAAug 2021 - Mar 2022

  • Led the clinical trial for a new cancer drug that was approved by the FDA, resulting in life-saving treatment for hundreds of patients.
  • Conducted research that led to the development of a new vaccine that has been shown to be effective in preventing the spread of disease.
  • Wrote and published a paper on my findings from a clinical study I conducted, which helped advance medical knowledge in this area.
  • Was part of a team that developed and implemented new guidelines for conducting clinical trials, which have now become standard practice.
  • Trained other researchers on how to conduct ethical and responsible clinical trials, ensuring patient safety is always paramount.

Education


Bachelor of Science in Biology at University of Washington, WAAug 2017 - May 2021

I have learned how to effectively communicate with others, how to work well in a team, how to manage my time wisely, and how to conduct research.

Skills


  • Clinical research
  • Regulatory affairs
  • Project management
  • Clinical data management
  • SAS programming
  • Good clinical practice (GCP) guidelines • ICH-GCP Guidelines

Chaniyah Szal

chaniyah.szal@gmail.com | (150) 369-1599 | Newark, NJ

Summary


I have over 1 year of experience as a Clinical Trial Associate. I am responsible for the management and coordination of clinical trials from start to finish. I have experience working with sponsors, CROs, and investigational sites. I am proficient in using EDC systems and other trial-related software. I am an excellent communicator and possess strong organizational skills.

Experience


Clinical Trial Associate at Johnson & Johnson, NJMar 2022 - Present

  • Led the clinical trial for a new cancer drug that resulted in a 70% success rate among participants.
  • Managed a team of 15 nurses and doctors during the course of the trial.
  • Wrote daily reports on progress and changes to be made to improve patient care.
  • Monitored patients' vitals signs and symptoms throughout the duration of their treatment.
  • Assisted in data analysis and interpretation at the conclusion of the study.

Clinical Trial Associate II at Bristol-Myers Squibb, NJJul 2021 - Jan 2022

  • Led the clinical trial for a new heart medication that was approved by the FDA, resulting in life-saving treatment for hundreds of thousands of people.
  • Successfully completed 100% of assigned tasks within timelines on average 98% of the time over 4 years.
  • Authored SOPs related to site activation and maintenance which were implemented company-wide, saving an estimated $100K annually.
  • Led training sessions for new CTAs, resulting in a 95% success rate for knowledge retention and skills development among trainees.
  • Managed 5 clinical trials simultaneously with teams ranging from 3-10 members each, ensuring all milestones were met on time and under budget.

Education


Bachelor of Science in Biology at Rutgers University, NJSep 2016 - May 2021

I have learned how to effectively communicate difficult concepts to people with little to no prior knowledge, how to work confidently and accurately in a laboratory setting and how to design and execute an experiment from start to finish.

Skills


  • Clinical research
  • Regulatory affairs
  • Project management
  • Data analysis
  • Clinical data management
  • SAS programming