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Novartis Pharmaceuticals - Pharmaceutical Resume Example

Alexa Coleman
Professional Summary
Experienced and accomplished licensed nurse with over 10 years of solid clinical healthcare experience.  Strong combination of medical information skills and customer service background.  Dedicated to achieving positive outcomes by helping to put life saving products into the marketplace.  
  • Customer and Personal Service
  • Critical Thinking
  • Monitoring
  • Complex Problem Solving
  • Troubleshooting
  • Clerical
  • Time Management
  • Service Orientation
Pharmaceutical Aug 2015Present Novartis Pharmaceuticals East Hanover , NJ
  • Customer Communication Center Analyst responsible for providing superior customer support in the areas of medical information, adverse event (both serious and non serious), product quality complaint reporting, and other processes as required.
  • Review medical literature and assess the article for seriousness according to FDA & ICH guidelines.
  • Attend and participate in marketed products interdisciplinary meetings as needed. 
  • Prepare minutes of relevant product information for call center team.
  • Reviewing medical device reports to determine accuracy to FDA.
  • Contribute to medical information baseline reports for annual reporting.
  • Assist with clinical compliance to SOPs, procedures and regulatory requirements by actively requesting and accurately completing required forms and documents.
  • Working knowledge of GCP Entering cases into a drug safety system and preparing cases for review and reporting as required by the FDA and worldwide regulatory authorities
Charge Nurse Aug 2013Present Tallwoods Care Bayville, NJ
  • Administer prescribed medications or start intravenous fluids, noting times and amounts on patients' charts.
  • Observe patients, charting and reporting changes in patients' conditions, such as adverse reactions to medication or treatment, and taking any necessary action.
  • Provide basic patient care or treatments, such as taking temperatures or blood pressures, dressing wounds, treating bedsores, giving enemas or douches, rubbing with alcohol, massaging, or performing catheterizations.
  • Sterilize equipment and supplies, using germicides, sterilizer, or autoclave.
  • Answer patients' calls and determine how to assist them.
  • Measure and record patients' vital signs, such as height, weight, temperature, blood pressure, pulse, and respiration.
  • Work as part of a healthcare team to assess patient needs, plan and modify care, and implement interventions.
  • Collect samples, such as blood, urine, or sputum from patients, and perform routine laboratory tests on samples.
  • Supervise nurses' aides or assistants.
  • Make appointments, keep records, or perform other clerical duties in doctors' offices or clinics.
  • Prepare patients for examinations, tests, or treatments and explain procedures.
    • Evaluate nursing intervention outcomes, conferring with other healthcare team members as necessary.
    Charge Nurse Sep 2007Mar 2015 Conmed Healthcare Inc Multiple Sites, NJ
    • Administer prescribed medications or start intravenous fluids, noting times and amounts on patients' charts.
    • Observe patients, charting and reporting changes in patients' conditions, such as adverse reactions to medication or treatment, and taking any necessary action.
      • Measure and record patients' vital signs, such as height, weight, temperature, blood pressure, pulse, and respiration.
      Clinical Research Associate (In house) Sep 2013Jun 2014 Covance Clinical Operations Princeton, NJ
      • Direct the preparation and submission of regulatory agency applications, reports, or correspondence.
      • Review all regulatory agency submission materials to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standards.
      • Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.
      • Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced.
      • Communicate regulatory information to multiple departments and ensure that information is interpreted correctly.
      • Manage activities such as audits, regulatory agency inspections, or product recalls.
      • Implement or monitor complaint processing systems to ensure effective and timely resolution of all complaint investigations.
      Clinical Trial Nurse Jan 2004Mar 2006 Trauma Nurses Princeton, NJ
      • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
      • Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
      • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
      • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
      • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
      • Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
      • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
      • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
      • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
      • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
      • Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
      • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
      • Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
      • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
      • Communicate with laboratories or investigators regarding laboratory findings.
      • Contact outside health care providers and communicate with subjects to obtain follow-up information.
      • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
      • Confer with health care professionals to determine the best recruitment practices for studies.
      Associate of Applied Science: Life Science Jun 2015 Ocean County College Toms River, NJ
      Nursing Jul 2005 Rowan College at Burlington County Pemberton, NJ
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      Resume Details

      This is a real resume for a Pharmaceutical in Barnegat, New Jersey with experience working for such companies as Novartis Pharmaceuticals, Tallwoods Care, Conmed Healthcare Inc. This is one of the hundreds of Pharmaceutical resumes available on our site for free. Use these resumes as templates to get help creating the best Pharmaceutical resume.

      Previous Companies:

      • Novartis Pharmaceuticals
      • Tallwoods Care
      • Conmed Healthcare Inc

      Previous Job Positions:

      • Pharmaceutical
      • Charge Nurse
      • Clinical Research Associate
      • Clinical Trial Nurse


      • Ocean County College
      • Rowan College at Burlington County

      Level of Education:

      • Associate of Applied Science

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