Clinical Research Assistant Resume Samples

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Clinical Research Assistants play an important role in clinical trials as they perform the actual testing of medications and medical devices. Usual duties mentioned on a Clinical Research Assistant resume include organizing files, handling correspondence, implementing operating procedures, following guidelines from ethics committees, and updating databases. Based on our collection of resume samples, essential skills for the job are computer competencies, multitasking, communication skills, teamwork, and accuracy. An Associate's or Bachelor's Degree in required for this position.

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1

Clinical Research Assistant

Accountable for overseeing Phase III clinical trials for 30 domestic transplant centers who are responsible for all post-transplant data submission to fulfill government contracts.

  • Acted as liaison for 150 world-wide transplant centers submitting data for NMDP clinical studies, IRB approval, and access into international donor registry.
  • Conducted monthly audits of research database, including an independent project related to cryopreservation of bone marrow and peripheral blood stem cells prior to transplant.
  • Resolved all research errors on data collection forms using medical terminology in order to convert data into tangible statistics which validate program integrity.
  • Improved quality control by documenting and submitting severe adverse event reports, protocol deviation forms, and quality improvement forms.
Candidate Info
7
years in
workforce
1
year
at this job
BS
Social Science
Clinical Research
2

Clinical Research Assistant

Directed MS Access patient database of 900+ eligible participants with Asthma and comorbidities

  • Adapted clinical research protocol and IRB amendments across 5 clinic sites in underserved New York communities
  • Created and adapted SQL queries to trends in clinical development and changes in EPIC best available practice queries
  • Conducted Spirometry tests to assess lung functionality and administer Cognitive and Health Literacy assessments
Candidate Info
7
years in
workforce
5
months
at this job
BA
Neuroscience And Behavior
3

Clinical Research Assistant

Supported the Regulatory Coordinator with the preparation of all regulatory documents for Pharmaceutical Companies, Clinical Research Organizations and Cooperative Groups.

  • Managed the patient information database for the Kimmel Cancer Center at [company name] to track patient records.
  • Provided support with "Monitoring and Close Out Visits" from pharmaceutical sponsors to ensure proper compliance.
  • Prepared and obtained signatures for IND safety reports ensuring patient safety.
  • Maintained short and long term follow-up information for Cooperative Group Studies.
  • Updated the Kimmel Cancer Center website with newly approved Clinical Trial information which resulted in availability on upcoming Clinical Trials.
  • Prepared Annual Reviews and Amendments for Cooperative Groups and Pharmaceutical Companies which were submitted to the Institutional Review Board for approval.
Candidate Info
3
years in
workforce
3
years
at this job
HS
High School Diploma
4

Clinical Research Assistant

Managed, as part of a team, one arm of a three-year clinical trial, responsibilities included trial design,
sample processing, sample quality control, and troubleshooting

  • Analyzed preliminary data using Excel, Prism, SigmaPlot, presented findings in PowerPoint regularly
  • Coordinated logistic operations with clinical centers, communicated with site supervisors
  • Organized and tracked over 4000 trial samples using Freezerworks
  • Praised by the supervisor of Pulmonary department in consecutive formal evaluations as effective in terms of performance, teamwork, communication, and time-management
Candidate Info
3
years in
workforce
2
years
at this job
BA
Biology
5

Clinical Research Assistant

Pre-Screened and Screened subjects to determine that clinical trial inclusion and exclusion was met prior to enrollment

  • Performed informed consent process following FDA GCP guidelines
  • Scheduled study visits to include Laboratory, ECG, MRI, ECHO and ultrasound appointments based on protocol schedule of assessments
  • Data collection and management, collection of source documents, using and developing CRFs, registration and management of AEs, filing and archiving, managing monitoring visits, dealing with queries.
  • Prepared lab kits and all required source documents for scheduled appointments
  • Collected required study data including adverse event and serious adverse events and reported as necessary to Sponsor and IRB within required time frame
Candidate Info
5
years in
workforce
3
years
at this job
BS
Nursing
6

Clinical Research Assistant

Actively worked in clinical research studies such as: ♦ Silent Myocardial Ischemia.
&b

  • Educates patients in significant aspects of the study. Ensured that the studies are conducted in accordance with the guidelines of the FDA and other regulatory agencies.
  • Working with Principal Investigator to develop and implement patient recruitment strategies.
  • Organized and maintained study database.
  • Participated in the development of new research protocols including design and data collection system.
  • Assist Principal Investigator with preparation of articles and for presentation
Candidate Info
6
years in
workforce
3
years
at this job
Medicine And Surgery
Hsc
7

Clinical Research Assistant

Facilitated the participation of patients on PI-initiated and industry clinical trials

  • Assisted with recruitment of participants in Phase 1 and Phase 2 trials
  • Prepared source documentation, physician orders and necessary specimen tubes for clinic visits
  • Processed, tracked and shipped specimens for testing; data entry of eCRFs and lab results in EDC and proprietary database
  • Created and maintained database with Excel to organize patient information and lab results
  • Scheduled and maintained travel and lodging itineraries, and coordinated clinic visits
Candidate Info
4
years in
workforce
4
years
at this job
BA
Biology
8

Clinical Research Assistant

Investigated/assisted with 5 clinical drug trials, supporting Physicians and PAs with patient care and follow up.

Helped room 5-10 patients per hour, took vital signs, and oversaw the accurate completion of paperwork and consent forms. Scheduled appointments and responded to inquiries. Aided Head of Clinical Research with home
based visits.

  • Complimented for quick ramp-up and self-motivation that provided opportunities for physicians to partake in additional trials. Personally read clinical trial manuals to rapidly advance skills and on-the-job training.
  • Established trust, interviewed patients, and answered questions to determine if clinical trial eligibility
  • Updated drug logs, placed orders for drugs/kits, and filled out paperwork for proper disposal. Performed
  • Participated in conflict of interest training for all clinical trial drugs: BIIB023, Xoma, Krystexxa, Allure
Candidate Info
5
months in
workforce
4
months
at this job
BS
Engineering Science And Mechanics With Biomechanics Concentration And Biomedical Engineering Minor
9

Clinical Research Assistant

UNC- CH Hospital
Chapel Hill, NC - Conducted neuropsychiatric and cognitive testing on all Memory Disorder Clinic patients

  • Assisted with patient visits for two clinical trial protocols
  • Collected and analyzed patient data in Access database for use in scientific journal articles
  • Processed blood/ urine samples in lab
  • Participated at outreach events for patients and caregivers affected by cognitive disorders
Candidate Info
9
years in
workforce
5
years
at this job
BS
Biology
10

Clinical Research Assistant II / Study Coordinator

Assisted Principle Investigators in conducting clinical trials using FDA approved practices and maintained the protection of human subjects while advancing trial goals.

  • Submitted invoices for applicable charges covered by funded research studies.
  • Served as site lead for all assigned clinical studies ensuring that studies are delivered according to Sponsor requirements on time and with high quality.
  • Prepared Institutional Review Board (IRB) materials related to initial review and approval of assigned studies.
  • Assisted with regulatory compliance including preparing IRB materials for approval of protocol amendments, as well as completing IRB continuing review reports.
  • responsibilities as Clinical Research Assistant for assigned trails in the Macular Function and Rose-Silverthorne Laboratory.
Candidate Info
5
years in
workforce
4
months
at this job
BS
Neuroscience

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