Clinical Project Manager, Late Phase Oncology
Current
Iqvia Biotech
Dec 2021 - Present
AeroLeads people directory · profile
Meredith Locklear Email & Phone Number
Clinical Project Manager, Late Phase Oncology
at
IQVIA Biotech
2 work emails found
@novellaclinical.com
1 phone found area 919
LinkedIn matched
✓ Verified Jun 2026
4 data sources
Profile completeness 100%
Current company
IQVIA Biotech
Role
Clinical Project Manager, Late Phase Oncology
Location
Durham, North Carolina, United States
Who is Meredith Locklear? Overview
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Quick answer
Meredith Locklear is listed as Clinical Project Manager, Late Phase Oncology at IQVIA Biotech, based in Durham, North Carolina, United States. AeroLeads shows a work email signal at novellaclinical.com, phone signal with area code 919, and a matched LinkedIn profile for Meredith Locklear.
Meredith Locklear previously worked as Associate Clinical Project Manager, Late Phase Oncology at Iqvia Biotech and Associate Technical Project Manager at Iqvia Biotech. Meredith Locklear holds Bachelor Of Science (Bs), Clinical Research from Campbell University.
Company email context
Email format at IQVIA Biotech
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{first}.{last}@novellaclinical.com
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AeroLeads found 2 current-domain work email signals for Meredith Locklear. Compare company email patterns before reaching out.
Profile bio
About Meredith Locklear
Meredith Locklear is a Clinical Project Manager, Late Phase Oncology at IQVIA Biotech. She possess expertise in powerpoint, microsoft excel, microsoft office, pharmaceutical industry, research and 6 more skills.
Listed skills include Powerpoint, Microsoft Excel, Microsoft Office, Pharmaceutical Industry, and 7 others.
Current workplace
Meredith Locklear's current company
Company context helps verify the profile and gives searchers a useful next step.
Iqvia Biotech
7 roles
Meredith Locklear work experience
A career timeline built from the work history available for this profile.
Associate Clinical Project Manager, Late Phase Oncology
Iqvia Biotech
Dec 2020 - Dec 2021
Associate Technical Project Manager
Iqvia Biotech
- Manages technical scope projects or works on larger technical projects under the supervision of a Technical Project Manager or above
- Responsible for change management on all assigned projects
- Responsible for assuring projects assigned are run according to SOPs and WPs as defined in the contract
- Responsible for assuring project timelines are met as per contract
- Responsible for maintaining client relationships for all assigned work, keeping all project reporting current, and assuring executive management is aware of issues putting Novella at financial or regulatory risk.
- Responsible for identifying, defining and documenting training requirements in LMS systems and assuring project level compliance with study specific training requirements
Oct 2018 - Dec 2020
Senior Project Coordinator
Iqvia Biotech
Apr 2017 - Oct 2018
Project Coordinator
Iqvia Biotech
- Responsible for supporting project management personnel through planning, implementation and effective execution of contracted clinical trials
- Responsible for supporting all project team members both administratively and technically, as appropriate
- Maintains support responsibility or provides directional oversight for Project Review Meetings, post-study review meetings, and other meetings, as assigned
- Responsible for initiating the collection of investigator site end user satisfaction information through an Investigative Site Satisfaction Survey, as applicable
- Assists in the development of project timelines and milestone tracking as directed by the Project Manager
- Provides project administrative support including meeting notes documentation, monthly reports, shipping, filing, tracking, and status summarization, as appropriate
Apr 2015 - Mar 2017
Project Assistant
Iqvia Biotech
- Responsible for supporting project management personnel through planning, implementation and effective execution of contracted clinical trials
- Responsible for supporting all project team members both administratively and technically, as appropriate
- Maintains support responsibility or provides directional oversight for Project Review Meetings, post-study review meetings, and other meetings, as assigned
- Responsible for initiating the collection of investigator site end user satisfaction information through an Investigative Site Satisfaction Survey, as applicable
- Assists in the development of project timelines and milestone tracking as directed by the Project Manager
- Provides project administrative support including meeting notes documentation, monthly reports, shipping, filing, tracking, and status summarization, as appropriate
Jun 2014 - Mar 2015
Project Coordination Intern
Iqvia Biotech
Jan 2014 - Jun 2014
1 education record
Meredith Locklear education
-
Campbell University
FAQ
Frequently asked questions about Meredith Locklear
Quick answers generated from the profile data available on this page.
What company does Meredith Locklear work for?
Meredith Locklear works for IQVIA Biotech.
What is Meredith Locklear's role at IQVIA Biotech?
Meredith Locklear is listed as Clinical Project Manager, Late Phase Oncology at IQVIA Biotech.
What is Meredith Locklear's email address?
AeroLeads has found 2 work email signals at @novellaclinical.com for Meredith Locklear at IQVIA Biotech.
What is Meredith Locklear's phone number?
AeroLeads has found 1 phone signal(s) with area code 919 for Meredith Locklear at IQVIA Biotech.
Where is Meredith Locklear based?
Meredith Locklear is based in Durham, North Carolina, United States while working with IQVIA Biotech.
What companies has Meredith Locklear worked for?
Meredith Locklear has worked for Iqvia Biotech.
How can I contact Meredith Locklear?
You can use AeroLeads to view verified contact signals for Meredith Locklear at IQVIA Biotech, including work email, phone, and LinkedIn data when available.
What schools did Meredith Locklear attend?
Meredith Locklear holds Bachelor Of Science (Bs), Clinical Research from Campbell University.
What skills is Meredith Locklear known for?
Meredith Locklear is listed with skills including Powerpoint, Microsoft Excel, Microsoft Office, Pharmaceutical Industry, Research, Project Management, Clinical Trials, and 21 Cfr Part 11.
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