Summary
Overview
Work History
Education
Skills
Clinical Trials Assistant Experience
Certification
Study Coordinator Experience
Clinical Research Associate Experience
Timeline
Generic

Jamie R. Rittel

Evansville,IN

Summary

With a combined 21 years of Clinical Research experience, currently working as a Senior Clinical Research Associate, Ms. Rittel has been a Lead Clinical Research Coordinator since 2005 with a background as a Licensed Practical Nurse since 2001. In 2015 she started working as a CTA and was quickly promoted to a CRA II within the first 4 months. She has knowledge in a wide range of therapeutic areas within Vaccine, Pediatrics, Infectious Disease, Neurodegenerative Disease, Dermatology, Urology, Rare Disease and General Medicine. Ms. Rittel has extensive experience in FDA audits on a site level and internal auditing across multiple projects on a monitor level.

Overview

20
20
years of professional experience
1
1
Certification

Work History

Independent Clinical Research Consultant

Compass Point Research
Indianapolis, IN
05.2025 - Current
  • Trained new staff on clinical research practices and regulatory requirements.
  • Implemented quality assurance measures to enhance research protocol adherence consistently.
  • Resolved queries raised by sponsors or regulatory authorities related to study processes or outcomes.

Senior Clinical Research Associate

ICON Clinical Research
Blue Bell, PA
08.2022 - 05.2025
  • Managed clinical trial operations, ensuring compliance with regulatory guidelines.
  • Conducted site visits to evaluate performance and adherence to study protocols.
  • Reviewed site regulatory binders for completeness and proper collection procedures.
  • Completed unblinded monitoring visits to oversee investigational product management and accountability.

Senior Clinical Research Associate 2

Syneos Health
Morrisville, NC
02.2021 - 08.2022
  • Reviewed and monitored data collection for accuracy and completeness.
  • Coordinated site selection and initiation for clinical research studies.
  • Conducted site visits to assess trial progress and resolve issues.
  • Reviewed site regulatory binder to check collection procedures and completeness of paperwork.
  • Completed unblinded monitoring visits to oversee investigational product management and accountability.

Senior Clinical Research Associate

IQVIA (formerly QuintilesIMS)
Durham, NC
08.2019 - 02.2021
  • Managed clinical trial operations and ensured compliance with regulatory guidelines.
  • Performed pre-study, closeout and interim visits to check on study activities.
  • Checked electronic data capturing systems for integrity and compliance.

Clinical Research Associate 2

Covance
Princeton, NJ
08.2018 - 08.2019
  • Adhered to good clinical practices, operating procedures and regulatory requirements.
  • Checked electronic data capturing systems for integrity and compliance.
  • Participated in internal audits related to clinical research operations processes.

Clinical Research Associate 2

IQVIA (formerly QuintilesIMS)
Durham, NC
09.2016 - 08.2018
  • Conducted site initiation visits and monitored ongoing studies at investigator sites.
  • Adhered to good clinical practices, operating procedures and regulatory requirements.
  • Identified experienced investigator through careful assessment to oversee conduct of trial at trial site.

Clinical Research Coordinator

Deaconess Clinic
Evansville, Indiana
03.2005 - 09.2015
  • Coordinated clinical trial activities, ensuring compliance with regulatory requirements.
  • Managed patient recruitment and informed consent processes for multiple studies.
  • Conducted screening interviews to assess eligibility of potential subjects.
  • Performed patient assessments, collected data, and prepared comprehensive reports.
  • Took vital signs and gathered medical histories according to study protocols.

Education

LPN - Practical Nursing Program

Ivy Tech State College
08.2001

Skills

  • Good clinical practice
  • Clinical trial management
  • Investigator selection and site monitoring
  • Quality assurance and regulatory compliance
  • Risk assessment and mitigation
  • Effective communication
  • Problem solving and critical thinking
  • Attention to detail
  • Task prioritization

Clinical Trials Assistant Experience

Phase 3-4, Hemophilia, Metastatic Cancer, Clinical Trials Assistant, CTA Responsibilities from Start-up to Close-out

Certification

  • Indiana Practical Nursing License, 27049725A, 2001
  • Certified Clinical Research Coordinator, Association of Clinical Research Professionals, 2011
  • ICH-GCP Accreditation, 2024

Study Coordinator Experience

Phase 1-4, NSCLC, Chemo-Induced Nausea, Metastatic Cancer, Osteoarthritis, Hypertensive Disorder, Hyperlipidemia, Depressive Disorder, Cardiovascular Disease, DM Type 2, Asthma, Psoriasis, Actinic Keratosis, Acne, Rosacea, Eczema, Onychomycosis, Atopic Dermatitis, Prostate Cancer, Cystitis, OAB, Bladder Cancer and BPH, Site CCRC, Study Coordinator Responsibilities from Start-up to Close-out

Clinical Research Associate Experience

  • Phase 1-3, Vaccine-Flu, COVID, RSV and Acne, Sr. Clinical Research Associate, Full blinded and unblinded CRA responsibilities, Start up to Close-out
  • Phase 1-2, Oncology - Multiple Myeloma, Malignant Solid Tumors, Sr. Clinical Research Associate II, Full CRA Interim Visit responsibilities
  • Phase 2/3, Respiratory Syncytial Virus, Senior Clinical Research Associate, CRA responsibilities from Start-up to Interim visits
  • Phase 3b, Type 2 Diabetes Mellitus with CV events, Clinical Research Associate II, CRA responsibilities from Interim visits to Close-out
  • Phase 3, Alzheimer's Disease, Clinical Research Associate II, CRA blinded and unblinded responsibilities from Start-up to Close-out
  • Phase 2, Non-Small Cell Lung Cancer, Clinical Research Associate II, Full unblinded CRA responsibilities from Interim visits to Close-out
  • Phase 2, Crohn's Disease, Clinical Research Associate II, CRA responsibilities from Interim visits to Close-out

Timeline

Independent Clinical Research Consultant

Compass Point Research
05.2025 - Current

Senior Clinical Research Associate

ICON Clinical Research
08.2022 - 05.2025

Senior Clinical Research Associate 2

Syneos Health
02.2021 - 08.2022

Senior Clinical Research Associate

IQVIA (formerly QuintilesIMS)
08.2019 - 02.2021

Clinical Research Associate 2

Covance
08.2018 - 08.2019

Clinical Research Associate 2

IQVIA (formerly QuintilesIMS)
09.2016 - 08.2018

Clinical Research Coordinator

Deaconess Clinic
03.2005 - 09.2015

LPN - Practical Nursing Program

Ivy Tech State College
Jamie R. Rittel
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