Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic

Margaret Graham

West Des Moines,IA

Summary

Knowledgeable RN adept at recognizing clinical values and abstract data from source documents. Use analytical skills to identify data or patient safety issues. Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials.

Highly organized, detail-oriented team player and thorough with good planning and problem-solving abilities. Certified in Oncology Nursing and have the ability to handle multiple projects simultaneously with a high degree of accuracy.

seeking a full-time position that offers professional challenges utilizing interpersonal skills, excellent time management, problem-solving skills and am ready to help team achieve its goals.

Overview

30
30
years of professional experience
1
1
Certification

Work History

Clinical Research Coordinator

Mission Cancer and Blood
05.2023 - Current
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed, and shipped lab specimens.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Followed informed consent processes and maintained records.
  • Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
  • Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
  • Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
  • Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
  • Maintained accurate and up-to-date case report forms and source documents for traceability.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.

Clinical Research Coordinator

Iowa Oncology Research Association
10.2015 - 05.2023
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Followed informed consent processes and maintained records.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Collected data and followed research protocols, operations manuals, and case report form requirement
  • Gathered, processed, and shipped lab specimens.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Collected, evaluated, and modeled collected data.
  • Demonstrated strong organizational and time management skills while managing multiple projects.
  • Used critical thinking to break down problems, evaluate solutions and make decisions.
  • Passionate about learning and committed to continual improvement.
  • Self-motivated, with strong sense of personal responsibility.
  • Developed and maintained courteous and effective working relationships.
  • Gained extensive knowledge in data entry, analysis and reporting.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.

Oncology Infusion Nurse

Medical Oncology Hematology Of Ottumwa
05.1994 - 10.2015
  • Leveraged knowledge of medications, procedures, infection control and safety precaution to initiate appropriate intervention in crisis situations.
  • Prepared chemotherapy doses for patient treatments as per physicians' orders.
  • Educated family members and caregivers on patient care instructions.
  • Counseled patients and provided listening ear and emotional support.
  • Assessed patients during course of treatment to identify concerning reactions.
  • Monitored patient reactions after administering medications and IV therapies.
  • Documented treatments delivered, medications and IVs administered, discharge instructions, and follow-up care.
  • Questioned patients to garner information about side effects, mobility and energy levels.
  • Recorded details regarding therapies to keep patient charts updated.
  • Explained course of care and medication side effects to patients and caregivers in easy-to-understand terms.
  • Educated patients on proper nutrition and medication side effects.
  • Administered IV fluids and medications to alleviate side effects from cancer treatment.
  • Followed all personal and health data procedures to effectively comply with HIPAA laws and prevent information breaches.
  • Remained current on advances in nursing care by participating in educational programs and oriented and educated new staff in nursing techniques and departmental procedures.
  • Evaluated patient histories, complaints, and current symptoms.

Education

Associate of Science - Nursing

Indian Hills Community College
Ottumwa, IA
05.1989

High School Diploma -

Ottumwa High School
Ottumwa, IA
05.1985

Skills

  • Good Clinical Practice
  • Medidata Rave
  • Site Visits
  • Potential Subject Evaluation
  • Case Report Management
  • Adverse Event Documentation
  • Specimen Collection
  • Study Coordination
  • Informed Consent
  • Documentation Management
  • Regulatory Requirements
  • Monitoring Visits
  • Phlebotomy
  • Specimen Coordination and Handling
  • Medication Dispensing
  • Participant Recruitment

Certification

Oncology Nursing Certification

Timeline

Clinical Research Coordinator

Mission Cancer and Blood
05.2023 - Current

Clinical Research Coordinator

Iowa Oncology Research Association
10.2015 - 05.2023

Oncology Infusion Nurse

Medical Oncology Hematology Of Ottumwa
05.1994 - 10.2015

Associate of Science - Nursing

Indian Hills Community College

High School Diploma -

Ottumwa High School

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Margaret Graham