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intern physician resume example with 3+ years of experience

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Jessica Claire
, , 100 Montgomery St. 10th Floor (555) 432-1000, resumesample@example.com
Professional Summary

Highly qualified medical research professional skilled in all aspects of clinical trial coordination, protocols, and participant relationships. Experienced in both medical practice and clinical research environments. Demonstrate strong working knowledge of ICH-GCP, company standard operating procedures, regulatory guidelines, protocols and monitoring guidelines. Communicate effectively with medical personnel, colleagues, and study participants. Consistently perform at peak professionalism, adhering to code of ethics and business standards. Experienced in multiple study areas, including diabetes, hypertension, gastrointestinal, gynecology, autoimmune disorders, cardiovascular, renal and psychiatry. Recognized for initiative, organization, time and task management, sound problem solving skills and flexibility.

Skills

    Competentin Written and Verbal English

    MSOffice Products (word, excel, power point)

    Fast Learner

    Adaptable

    Flexible

    Extreme Attention to Detail

    Ability to Travel without Limitations

    Strong Knowledge of Medical Terminology

    ElectronicMedical Records

    Documentation& Reporting

    Strong Work Ethic

    Time Management

Work History
01/2015 to 10/2016 Intern Physician Johnson & Johnson | Syracuse, NY,

Delivered comprehensive, compassionate patient care, including testing and evaluation, medication administration, progress monitoring, and treatment planning.  

Increased Patient compliance with office visits and medication by 55%.

Educated community members and patients on disease prevention, diet, and hygiene.  

Trained, supervised and evaluated healthcare providers, nursing, and office staff, ensuring quality and integrity of practice and patient service.  

Managed office staff on patient retention and rapport.

Encouraged complete routine administrative task and patient services in a timely manner.

Cultivated productive relationships with patients, families, and healthcare professionals, optimizing patient progress in meeting short and long-term wellness goals.  

Actively engaged in professional development, deepening awareness of current developments in clinical research and healthcare.  

Showed commitment to and performed consistently in high performance environment

Maintained patient/client focused approaches to work with the ability to interact professionally within a patient/client organization and provide presentations.

Possessed willingness to work in a diverse environment and value the importance of teamwork.


07/2012 to 07/2013 Clinical Research Associate/Assitant Atlanta Center For Medical Research | City, STATE,

Maintained working knowledge of and ensured compliance with applicable ICH-GCP Guidelines, local regulatory requirements, SOPs, and study specific procedures. 

Creating and maintaining screen books and charts for all assigned studies

Prepare visits for the next day, ensuring accuracy of source documents and assessments

Filing of lab results, EKG results, and other communication in designated charts

Timely completion of data entry for all eCRFs, as well as paper CRF completion and transmission

Documented and conducted appropriate correspondence regarding adverse events, including multiple severe adverse events

Ensured study documents are tracked, file, maintained, and archived in audit-ready condition

Aided in the facilitation of study monitoring visits

Built relationships with investigators and site staff 

Participated in Investigator and other external or internal meetings as required

Performed on-site facility inspection



07/2011 to 07/2012 Clinical Research Coordinator Centura Health | City, STATE,

Maintained working knowledge of and ensured compliance with applicable ICH-GCP Guidelines, local regulatory requirements, SOPs, and study specific procedures.

Maintained compliance with required trainings in the Learning Management System (LMS/E-Learning). 

Performed all tasks relevant to study participant selection, including written and oral consent, screening and educating subjects, caregivers, and referral sources on protocol specific details and expectations.  

Expertly conducted full range of patient and protocol assessments, including safety and efficacy, vital signs and EKGs.  

Active contributor in investigator/sponsor and coordinator meetings, sharing valuable study data and insight as requested.  

Communicated professionally to internal and external study teams the performance of recruitment tactics.

Increased study engagement both with patients and site staff along with support study compliance requirements to meet sponsor goals.

Adapt to new and innovative solutions for patient recruitment challenges and fast-paced environments.

Maintenance of study regulator documents, including screening and enrollment logs, drug accountability logs, subject identification logs, site signature logs 

Completion of case report forms (CRFs) 

Coordinate and oversee clinical assessments of clients participating in clinical trial studies of major depression, hypertension and diabetic medications


Education
Expected in to to Master of Science | Health Information Management CUNY School of Profesinal Studies , New York, NY, GPA:
Expected in 06/2012 to to Bachelor of Arts | Anthropology CUNY The City College of New York, New York, NY, GPA:
Certifications
ICH Good Clinical Practice (GCP) | Cardiopulmonary Resuscitation (CPR)  Health Insurance Portability and Accountability Act (HIPAA) | Blood Borne Pathogens Certification

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Resume Overview

School Attended

  • CUNY School of Profesinal Studies
  • CUNY The City College of New York

Job Titles Held:

  • Intern Physician
  • Clinical Research Associate/Assitant
  • Clinical Research Coordinator

Degrees

  • Master of Science
  • Bachelor of Arts

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