Study Coordinator

Writing a great study coordinator 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 study coordinator 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 study coordinator job you're after.

Resume samples

Tearia Rodil

tearia.rodil@gmail.com | (292) 613-1158 | 1065 NW Johnson St, Portland, OR 97209, USA

Summary


I am a study coordinator with over three years of experience. I have worked in both clinic and research settings, which has allowed me to develop strong coordination skills. I am detail-oriented and efficient, able to manage multiple tasks simultaneously. I have excellent communication and organizational skills, as well as the ability to work independently. I am confident in my abilities and would be an asset to any team

Experience


Senior Study Coordinator at Pacific Clinical Research Center, ORApr 2022 - Present

  • Led a team of 5 study coordinators in the successful implementation of clinical research studies.
  • Recruited and enrolled 100 patients into a clinical trial within 6 months.
  • Monitored 10 patient cases per week and addressed any issues that arose.
  • Trained new staff on proper procedures for conducting clinical trials.
  • Wrote standard operating procedures (SOPs) for various aspects of the clinical trial process.
  • Kept detailed records of all patient data and entered it into the electronic database.

Study Coordinator at Willamette Valley Cancer Institute and Research Center, ORAug 2019 - Mar 2022

  • Successfully recruited 400 participants for a clinical study in 4 months.
  • Coordinated schedules for 20+ staff members and 100+ patients.
  • Maintained budget of $50,000 throughout the duration of the study.
  • Created and implemented new policies that improved patient retention by 15%.
  • Increased departmental efficiency by 30% through process improvements.
  • Authored SOPs that are now used company-wide.

Education


Bachelor of Science in Health Studies at Oregon State UniversityAug 2015 - May 2019

I have learned how to effectively communicate with people from diverse backgrounds, how to manage my time efficiently, and how to critically analyze information.

Skills


  • Research
  • Data Analysis
  • Project Management
  • Clinical Trials Experience
  • Good Communication Skills
  • Detail Oriented

Vivien Woods

vivien.woods@gmail.com | (500) 177-6075 | Wichita, KS

Summary


I am a study coordinator with over 3 years of experience in the field. I have worked on a variety of studies, both clinical and research-based. My role is to oversee all aspects of the study, from start to finish. This includes working with the principal investigator to develop the protocol, coordinating site activities, monitoring patient progress, and ensuring data quality. I have a keen eye for detail and thrive in fast-paced environments. I am an excellent communicator and have superb organizational skills

Experience


Senior Study Coordinator at Syneos Health, KSMar 2022 - Present

  • Led the development and implementation of a new clinical research study protocol which resulted in an increase of patient participation by 20%.
  • Successfully recruited 50 patients for a clinical trial studying the effects of a new cancer treatment drug.
  • Monitored 10 patients closely during their participation in a long-term study on heart disease.
  • Completed all necessary paperwork and documentation for 15 different studies being conducted simultaneously.
  • Trained 5 new junior staff members on proper research protocols and procedures.

Study Coordinator at PRA Health Sciences, KSSep 2019 - Jan 2022

  • Led a team of 5 study coordinators in conducting clinical research trials.
  • Coordinated the scheduling and logistics for 50+ patient visits per week.
  • Entered and managed data for 10 active studies in REDCap database.
  • Trained 2 new study coordinators on site procedures and Good Clinical Practice guidelines.
  • Authored 3 Standard Operating Procedures related to clinical trial conduct.

Education


Bachelor of Science in Health Studies at University of KansasSep 2015 - May 2019

Through my degree I have learned excellent research, writing, and communication skills.

Skills


  • Excellent organizational skills
  • Strong written and verbal communication skills
  • Ability to work independently and as part of a team
  • Detail-oriented with strong analytical skills
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Experience coordinating research studies preferred