ANGELA KEAN
Arnold
Summary
Dynamic Clinical Research Coordinator with extensive experience at Clinical Research Professionals, adept at managing trial protocols and ensuring patient safety. Skilled in informed consent and adverse event tracking, I excel in participant screening and documentation, fostering collaboration among healthcare teams to achieve timely study completion and enhance data accuracy.
Overview
9
9
years of professional experience
Work History
Clinical Research Coordinator
Clinical Research Professionals
12.2022 - Current
- 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.
- Followed informed consent processes and maintained records.
- Gathered, processed, and shipped lab specimens.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Prepared and maintained regulatory documents for clinical trial submissions.
Clinical Research Coordinator
Sundance Clinical Research
02.2019 - 12.2022
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Maintained accurate and up-to-date case report forms and source documents for traceability.
- 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.
- Followed informed consent processes and maintained records.
- Gathered, processed, and shipped lab specimens.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Prepared and maintained regulatory documents for clinical trial submissions.
Registered Medical Assistant
Signature Orthopedics
10.2016 - 02.2019
- Prepared and administered medications to alleviate patient symptoms.
- Called and faxed pharmacies to submit prescriptions and refills.
- Promoted office efficiency, coordinating charts, completing insurance forms, and helping patients with diverse needs.
- Directed patients to exam rooms, fielded questions, and prepared for physician examinations.
- Assisted with routine checks and diagnostic testing by collecting and processing specimens.
- Taught patients about medications, procedures, and care plan instructions.
- Enhanced patient outcomes by providing knowledgeable education on procedures, medications, and other physician instructions.
- Collected and documented patient medical information such as blood pressure and weight.
- Obtained client medical history, medication information, symptoms, and allergies.
- Assisted physicians with minor surgeries, including preparing operating room and sterilizing instruments.
- Explained procedures to patients to reduce anxieties and increase patient cooperation.
Education
GED -
Windsor High School
Imperial, MOSkills
- Adverse event tracking
- Dispensing oversight
- Study protocols
- Phlebotomy
- Laboratory results management
- Informed consent
- Trial management
- Documentation requirements
- Specimen handling
- Case report management
- Participant screening
- Medication dispensing
Timeline
Clinical Research Coordinator
Clinical Research Professionals
12.2022 - Current
Clinical Research Coordinator
Sundance Clinical Research
02.2019 - 12.2022
Registered Medical Assistant
Signature Orthopedics
10.2016 - 02.2019
GED -
Windsor High School