junior resident doctor resume example with 8 years of experience

(555) 432-1000,
, , 100 Montgomery St. 10th Floor

Multi-talented clinical research professional experienced in complying with study protocols, standard operating procedures and good clinical practices for different clinical trials. Well-organized and hardworking with excellent communication and planning skills. Prepared to offer five years of experience in the field and take on a fast-paced position.

  • Trial Oversight
  • Case Report Management
  • Specimen Handling
  • Documentation Requirements
  • Research Experience
  • Computer Skills
  • Planning & Organizing
  • Protocols Development
  • Friendly, Positive Attitude
  • Detailed Documentation
  • Patient Safety
  • Clinical Documentation
  • Laboratory Results Management
  • Dispensing Oversight
Education and Training
University of Ibadan Oyo State, Nigeria, Expected in 02/2017 Master of Science : Pharmarcology And Therapeutics - GPA :
Sumy State University Ukraine, Expected in 07/2011 M.D. : Medicine - GPA :
University of Ibadan Ibadan, Nigeria, Expected in Ph.D. in View : Pharmarcology And Therapeutics - GPA :
Albert Einstein College Of Medicine - Junior Resident Doctor
Bronx, NY, 07/2019 - 10/2022
  • Provided patient diagnosis, test evaluation and treatment under strict time constraints.
  • Prescribed medications, explaining side effects and possible adverse reactions to keep patients informed and alert to potential issues
  • Prescribed medications and other therapeutic interventions to treat and prevent different illnesses.
  • Collaborated closely with fellow medical team members to share knowledge and discuss best courses for treatment.
  • Prescribed medications and advised patients about dosage, schedule and possible side effects.
  • Interviewed patients about symptoms and conducted thorough physical examinations.
Community Health Network - Study Coordinator
Avon, IN, 04/2021 - 01/2022
  • Adhered to good clinical practices, operating procedures, and regulatory requirements in data collection, research protocols, and regulatory reporting.
  • Developed standard operating protocols, source documents, and case report form to standardise operations.
  • Prepared, reviewed, submitted, and maintained IRB/EC submissions and communications.
  • Coordinated and supervised the screening and recruitment of potential research study participants.
  • Provided documentation and communication and maintained essential documents.
  • Communicated with vendors to deliver appropriate clinical supplies to meet operational demands.
  • Attended investigator meetings to provide a framework for successful research studies by establishing responsibilities.
  • Worked successfully with a diverse group of co-workers to accomplish goals and address issues related to the trial.
  • Worked closely with team members to deliver project requirements, develop solutions, and meet deadlines.
  • Administered financial operations, expenditure authorisation, accounting, and financial reporting.
Brewer Science - Clinical Research Assistant
Rolla, MO, 10/2014 - 07/2019
  • Developed study protocols, informed consent forms, and case report form to standardise operations.
  • Adhered to standards in areas involving data collection, research protocols, regulatory reporting, and compiling of vital documentation
  • Supervised participant screening, recruitment, enrollment, and follow-up
  • Analysed records, exam data, and test results to inform diagnoses.
  • Kept patient care protocols and clinical trial operations in compliance with good clinical practice and regulations.
  • Conducted routine laboratory tests and sample analyses to monitor disease response.
  • Held weekend and evening sessions according to project specifications and workload.
  • Collated, reviewed, and analysed study data with Excel and SPSS (qualitative and quantitative).
  • Maintained strict confidentiality to keep personal information and collected data private.
  • Participated in educational training, activities, and professional development programs.
  • Juggled multiple projects and tasks to ensure high-quality and timely delivery.
  • Managed administrative and office operations, including supervision of other team members, financial appropriation, budget disbursement, and post-research evaluation/ audit.
  • Prepared, reviewed, submitted, and managed IRB/EC communications and submissions.
Nmn, - Senior Research Associate
, , -
  • Leveraged SPSS qualitative analysis software to identify data set correlations while performing qualitative functions.
  • Planned, executed and monitored projects pertaining to [Type of Project] as directed by the [Job Title]
  • Identified relevant questions and determined best methods of collection.
  • Participated in regulatory activities and submission by adhering to independent ethics committee and regulatory board.Conducted independent research to assimilate results for technical reports and publications.
  • Organized data in logical ways to enable efficient analysis and effective communication of findings.
  • Utilized [Type of Software] to input data gathered from various sources and compile into detailed reports that were disseminated to proper project staff.
  • Identified potential threats to properly manage project risks.

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Resume Overview

School Attended

  • University of Ibadan
  • Sumy State University
  • University of Ibadan

Job Titles Held:

  • Junior Resident Doctor
  • Study Coordinator
  • Clinical Research Assistant
  • Senior Research Associate


  • Master of Science
  • M.D.
  • Ph.D. in View

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