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medical research analyst medical writer resume example with 19+ years of experience

Jessica Claire
, , 609 Johnson Ave., 49204, Tulsa, OK 100 Montgomery St. 10th Floor
Home: (555) 432-1000 - Cell: - resumesample@example.com - : - -
Summary

Organized and results-oriented healthcare professional with extensive background in proprietary medical writing and 7+ years of clinical research experience. Proficient at healthcare data analysis and the incorporation of evidence-based medicine to produce high-quality medical documents with scientific accuracy. Adept at managing concurrent projects to promote efficiency and desired outcomes in a timely manner. Integral team player with excellent communication skills and strong problem-solving ability.

Skills
  • Disease Trends
  • Data Collection and Analysis
  • Medical Writing
  • Organization and Time Management
  • Teamwork and Collaboration
  • Problem Solving
  • MS Office Proficiency
  • Document Library Development
  • Flexible and Adaptable
  • Multitasking
  • Project Management
  • Creative, Resourceful, and Efficient
  • Excellent Interpersonal and Communication Skills
Experience
2013 to Current
Medical Research Analyst/Medical Writer Dova Pharmaceuticals, Inc. Durham, NC,
  • Conducted analysis of Evidence-Based Medical studies for proprietary publication to measure the effectiveness of current medical, clinical, and pharmaceutical practices against gold standards of treatment.
  • Wrote articles and reports on research discoveries connected to health and medical fields.
  • Drafted and edited high quality, medically accurate manuscripts, conference abstracts and posters.
  • Advised and consulted with internal and external stakeholders on areas of expertise.
  • Created high-quality content for publication in journals or presentations at meetings to support products, research activities and business needs.
  • Translated clinical trial results, patient-reported outcomes data and health economics analysis into written and visual communications.
  • Designed slide decks and digital content to support publications and medical affairs activities.
  • Prioritized tasks, worked simultaneously on multiple projects, and completed high-quality documents according to tight timelines.
2009 to 2013
Medical Science Liaison Freelancers Union City, STATE,
  • Built professional relationships with healthcare professionals, researchers and academic centers of excellence to access current and emerging information in areas of Immunology, Infectious Disease, and Endocrinology.
  • Partnered with and consulted researchers, physicians, and academic centers of excellence to access current and emerging information in healthcare.
  • Reviewed and critiqued scientific publications to remain informed of healthcare trends in Internal Medicine.
  • Obtained and reviewed data and information from scientific publications and literature.
  • Evaluated information and analyzed data to draw conclusions and present findings to scientific community and public.
  • Documented and published articles in professional proprietary publications.
  • Developed medical information literature and slide decks.
  • Played pivotal role in helping to develop content with high degree of medical accuracy, functionality, and usability on time and on budget.
  • Functioned as primary contact for investigators interested in developing and conducting physician-initiated clinical studies.
  • Communicated large amounts of complex scientific content in clear and concise terminology.
  • Identified and supported potential research expansion projects, collaborations, medical advisors and educational partnership opportunities.
2008 to 2009
Medical Research Analyst Hayes Healthcare Assessment City, STATE,
  • Compiled and organized research data to produce reports and graphs.
  • Partnered with and consulted researchers, physicians, and academic centers of excellence to access current and emerging information in healthcare.
  • Reviewed and critiqued scientific publications to remain informed of healthcare trends in Internal Medicine.
  • Obtained and reviewed data and information from scientific publications and literature.
  • Evaluated information and analyzed data to draw conclusions and present findings to scientific community and public.
  • Documented and published articles in professional proprietary publications.
  • Developed medical information literature and slide decks.
  • Played pivotal role in helping to develop content with high degree of medical accuracy, functionality, and usability on time and on budget.
  • Functioned as primary contact for investigators interested in developing and conducting physician-initiated clinical studies.
  • Communicated large amounts of complex scientific content in clear and concise terminology.
  • Identified and supported potential research expansion projects, collaborations, medical advisors and educational partnership opportunities.
2003 to 2008
Clinical Research Associate I/II Brown University/LifeSpan City, STATE,
  • Performed and documented pre-study site evaluations, site initiations and interim monitoring, document collection, follow-ups, and study close-out visits.
  • Supported team in developing research protocol.
  • Organized, analyzed, and modeled study data.
  • Conducted research activities according to FDA Regulations regarding ICH/GCP guidelines, SOPs, as well as local requirements.
  • Ensured site IRB approval was current and all IRB documentations were in order.
  • Monitored and reported all Serious Adverse Effects (SAE) to IRB.
  • Submitted accurate and timely routine clinical visit reports.
  • Performed regulatory document collection: gathered, prepared, and maintained appropriate information using standard protocol; adhering to federal guidelines to insure Quality Control (QC)patient safety, internal consistency, and data reliability.
  • Maintained drug accountability, strict control over investigational drugs; and maintained highest ethical standards in areas involving data collection, research protocols, and regulatory reporting.
  • Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
  • Attended Investigator Meetings and made presentations.
  • Reviewed clinical data and independently performed CRF reviews.
  • Ensured resolution of issues with investigative sites.
  • Updated and maintained information accuracy within patient database.
  • Obtained informed consent from research subjects and guardians; explained possible SAE and potential outcomes of clinical research.
  • Conducted patient interviews to gather health history, vital signs, and information about current medical issues.
  • Educated clinical study participant and addressed concerns.
  • Transmitted physician's orders to patients, counseling on execution and addressing follow-up questions.
  • Communicated with patients by phone and via written correspondence.
  • Adhered to good clinical practices, operating procedures and regulatory requirements.
Education and Training
Expected in to to
Bachelor of Science: Biology
Tougaloo College - Tougaloo, MS,
GPA:
Expected in to to
M.D.:
Brown University, Alpert Medical School - Providence, RI,
GPA:

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Resume Overview

School Attended

  • Tougaloo College
  • Brown University, Alpert Medical School

Job Titles Held:

  • Medical Research Analyst/Medical Writer
  • Medical Science Liaison
  • Medical Research Analyst
  • Clinical Research Associate I/II

Degrees

  • Bachelor of Science
  • M.D.

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