Christopher Sleeper
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Christopher Sleeper Email & Phone Number

IBC Community Member at ADVARRA IBC
Location: Dewitt, Michigan, United States 9 work roles 3 schools
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✓ Verified May 2026 3 data sources Profile completeness 86%

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Current company
ADVARRA IBC
Role
IBC Community Member
Location
Dewitt, Michigan, United States

Who is Christopher Sleeper? Overview

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Quick answer

Christopher Sleeper is listed as IBC Community Member at ADVARRA IBC, based in Dewitt, Michigan, United States. AeroLeads shows a matched LinkedIn profile for Christopher Sleeper.

Christopher Sleeper previously worked as Clinical Research Associate at Parexel and Project Leader at Be Well Medical Center. Christopher Sleeper holds Biology/Chemistry from Lake Superior State University.

Profile bio

About Christopher Sleeper

I have worked in the CRO and pharmaceutical industry for over 12 years. My areas of expertise are Oncology and HIV. Specialties include performing and coordinating external and internal clinical studies, with emphasis on site selection, site initiation and training, protocol development, and study closeout. Adept at working with central and local Institutional Review Boards, and well-versed in Good Clinical Practice, ICH guidelines, federal regulations, and Standard Operating Procedures.

Current workplace

Christopher Sleeper's current company

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ADVARRA IBC
Advarra Ibc
IBC Community Member
9 roles

Christopher Sleeper work experience

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Ibc Community Member

Current
Advarra Ibc

Columbia, MD

-Attend assigned meetings via videoconference. ∙ Prepare for each IBC meeting. Read the non-technical abstract and review all submission materials.∙ Participate in relevant discussion during committee meetings, particularly as they relate to community. and the environment. ∙ Vote on each item presented to the committee.

Jul 2021 - Present

Clinical Research Associate

Billerica, Massachusetts, United States

Conduct site monitoring of clinical trials, according to SOP's, ICH guidelines and GCP, including pre study, site initiation, routine monitoring, and close-out visits. ∙ Perform clinical on-site monitoring activities (drive patient recruitment, source date verification, drug accountability, data collection) ∙ Collect regulatory documentation.∙ Mentor new.

Sep 2021 - Jan 2024

Project Leader

Berkley, Michigan, United States

-Inform patients or research staff about study aspects and outcomes to be expedited. ∙ Code, evaluate, or interpret collected study data. ∙ Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional policies. ∙ Communicate with laboratories or investigators about laboratory.

Jul 2018 - Mar 2021

Clinical Research Associate Ii

Morrisville, North Carolina, United States

-Conduct site monitoring of clinical trials, according to SOP's, ICH guidelines and GCP, including pre study, site initiation, routine monitoring, and close-out visits. ∙ Perform clinical on-site monitoring activities (drive patient recruitment, source date verification, drug accountability, data collection) ∙ Collect regulatory documentation. ∙ Protect.

May 2018 - Jun 2018

Clinical Research Associate Ii

Princeton, New Jersey, United States

-Conduct site monitoring of clinical trials, according to SOP's, ICH guidelines and GCP, including pre study, site initiation, routine monitoring, and close-out visits. ∙ Perform clinical on-site monitoring activities (drive patient recruitment, source date verification, drug accountability, data collection) ∙ Collect regulatory documentation. ∙ Protect.

Jul 2015 - Nov 2017

Clinical Research Associate

Quintiles

Kansas City, Missouri, United States

Conduct site monitoring of clinical trials, according to SOP's, ICH guidelines and GCP, including pre study, site initiation, routine monitoring, and close-out visits. ∙ Perform clinical on-site monitoring activities (drive patient recruitment, source date verification, drug accountability, data collection) ∙ Collect regulatory documentation. ∙ Protect.

Jul 2014 - Jun 2015

Clinical Studies Coordinator

Intervention Insights

Grand Rapids, Michigan, United States

Presented Intervention Insights’ technology to hospitals and insurance groups, resulting in successful rate of partnership. ∙ Provided final subject approval for protocol entry. ∙ Monitored all subject data provided to Intervention Insights.

Aug 2011 - Jul 2012

Inpatient Pharmacy Technician

Lansing, Michigan, United States

- Physician Order Entry-Drug Compounding-IV Admixture

Aug 2003 - Aug 2011

Study Coordinator/Clinical Research Associate

Sparrow Regional Cancer Center

Lansing, Michigan, United States

∙ On-stie drug accountability and reconciliation.∙ Audit preparation and execution. ∙ Patient screening. ∙ Data management. ∙ Local IRB/Regulatory affairs.-Monitor PI Initiated Protocols

Feb 2008 - Jul 2011
3 education records

Christopher Sleeper education

FAQ

Frequently asked questions about Christopher Sleeper

Quick answers generated from the profile data available on this page.

What company does Christopher Sleeper work for?

Christopher Sleeper works for ADVARRA IBC.

What is Christopher Sleeper's role at ADVARRA IBC?

Christopher Sleeper is listed as IBC Community Member at ADVARRA IBC.

Where is Christopher Sleeper based?

Christopher Sleeper is based in Dewitt, Michigan, United States while working with ADVARRA IBC.

What companies has Christopher Sleeper worked for?

Christopher Sleeper has worked for Advarra Ibc, Parexel, Be Well Medical Center, Syneos Health Clinical Solutions, and Covance.

How can I contact Christopher Sleeper?

You can use AeroLeads to view verified contact signals for Christopher Sleeper at ADVARRA IBC, including work email, phone, and LinkedIn data when available.

What schools did Christopher Sleeper attend?

Christopher Sleeper holds Biology/Chemistry from Lake Superior State University.

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