Annisha Samson
Kansas City,MO
Summary
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Overview
12
12
years of professional experience
Work History
Sr Clinical Trial Enrollment Coordinator
ICON
07.2019 - Current
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records and databases to identify prospective candidates for research studies.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Followed informed consent processes and maintained records.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines.
- Created study specific recruitment materials per protocol for IRB compliance and submission.
- Identified issues, analyzed information and provided solutions to problems.
- Participated in team projects, demonstrating an ability to work collaboratively and effectively.
- Mentored new hires, resulting in stronger staff development and increased productivity.
Recruitment Specialist
ICON
03.2017 - 07.2019
- Worked with principal investigator and study team to ensure compliance with protocols covering patient care and clinical trial operations.
- Collected, evaluated, and modeled collected data.
- Tracked patient laboratory results and screening data.
Medical Research Associate II
ICON
07.2015 - 03.2017
- Assisted in the informed consent process.
- Obtained client medical history, medication information, symptoms, and allergies.
- Documented vital signs and health history and perform venipuncture and ECG's for patients in clinic environments.
- Verified eligibility of patient based on study protocol requirements.
- Oriented and trained new staff on proper procedures and policies.
- Worked in conjunction with the clinical study manager as a study lead providing the expert knowledge of assigned study protocols.
- Monitored and reported trainee progress, introducing new learning tools to address individual needs.
Medical Assistant
ICON
07.2011 - 07.2015
- Sanitized, restocked, and organized exam rooms and medical equipment.
- Directed patients to exam rooms, fielded questions, and prepared for physician examinations.
- Obtained client medical history, medication information, symptoms, and allergies.
- Performed medical records management, including filing, organizing and scanning documents.
- Kept medical supplies in sufficient stock by monitoring levels and submitting replenishment orders before depleted.
Education
Medical Assisting Certificate -
Concorde Career College
Kansas City, MOSkills
- Team Leadership Skills
- Scheduling Appointments
- Confidentiality Understanding
- Office 365
- Clinspark, Trial one, Clinical Ink
- Verified Clinical Trials
- ICH-GCP
Timeline
Sr Clinical Trial Enrollment Coordinator
ICON
07.2019 - Current
Recruitment Specialist
ICON
03.2017 - 07.2019
Medical Research Associate II
ICON
07.2015 - 03.2017
Medical Assistant
ICON
07.2011 - 07.2015
Medical Assisting Certificate -
Concorde Career College