Summary
Overview
Work History
Education
Skills
Hobbies
Timeline
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JACOB SEKINGER

Cincinnati,United States

Summary

Knowledgeable Clinical researcher adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Recognized consistently for performance excellence and contributions to success in the life sciences industry. Strengths in Clinical trials, regulatory compliance, and professional interactions with patients backed by training in Biological sciences. Ready to bring 3 years of related experience to a challenging new role.

Overview

3
3
years of professional experience

Work History

Clinical Trial Educator

IQVIA
Cincinnati, Ohio
11.2021 - Current
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Engaged research sites and surrounding communities to keep the study at the top of mind while also looking for patient recruitment opportunities

Clinical Research Coordinator III

Cincinnati Children's Hospital
Cincinnati, Ohio
01.2021 - Current
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Maintain and oversee 7 Clinical trials while leading 4 trials
  • Maintain awareness of status of all active studies through thorough communication with medical professionals and clinical research professionals
  • Followed informed consent processes and maintained records.

Clinical Research Coordinator

Velocity Clinical Research
Cincinnati , Ohio
08.2020 - 01.2021
  • Lead 2 Clinical trials while supporting 2 other clinical trials.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Supported 2 high profile clinical trials, including Moderna and Pfizer, by scheduling and seeing up to 15 patients each day to ensure progression and collection of data to provide to sponsors
  • Schedule monitor visits and set up for monitoring visits prior to internal monitoring visits.
  • Improved operations through consistent hard work and dedication.

Regulatory Submissions Coordinator

Medpace
Cincinnati, Ohio
08.2019 - 04.2020
  • Managed full life cycle of assigned audits in alignment with departmental procedures, delivering progress as well as closing reports to senior management and clients.
  • Publicized health and safety program requirements and mentored employees on critical nature of compliance.
  • Collecting, reviewing, organizing, and assembling regulatory documents for study start-up.
  • Collaborated with national team to push study startup for 11 studies
  • Provided exceptional support to internal and external team members for compliance of regulations and requirements.

Education

Bachelor of Science - Biological Sciences

University of Cincinnati
Cincinnati, OH
08.2019

Skills

  • Trial Management
  • Patient Care
  • Organization
  • Critical thinking

Hobbies

Avid outdoorsman with experience in Sport climbing, long distance backpacking, and mountaineering

Timeline

Clinical Trial Educator

IQVIA
11.2021 - Current

Clinical Research Coordinator III

Cincinnati Children's Hospital
01.2021 - Current

Clinical Research Coordinator

Velocity Clinical Research
08.2020 - 01.2021

Regulatory Submissions Coordinator

Medpace
08.2019 - 04.2020

Bachelor of Science - Biological Sciences

University of Cincinnati

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JACOB SEKINGER