Meredith Locklear Email & Phone Number
@novellaclinical.com
1 phone found area 919
LinkedIn matched
Who is Meredith Locklear? Overview
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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.
Email format at IQVIA Biotech
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AeroLeads found 2 current-domain work email signals for Meredith Locklear. Compare company email patterns before reaching out.
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.
Meredith Locklear's current company
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Meredith Locklear work experience
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Associate Clinical Project Manager, Late Phase Oncology
Associate Technical Project Manager
• 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 through the approved upon pathways for reporting• Responsible for identifying, defining and documenting training requirements in LMS systems and assuring project level compliance with study specific training requirements• Assists in communication of budget allocations and approval of invoices• Participates and assists in the planning and creation of client related materials as per contract• Oversee delegation of support staff activities, as necessary of Associate Technical PM• Supports Contracts and Proposals with final project contract execution and CIS documentation by the project teamAuthorized to: •Hold client deliverables when deemed appropriate for financial or quality reasons •Negotiate deliverable timelines with clients leading to contract amendments •Negotiate scope of work agreement with clients. (Cannot authorize variances to the scope of work)• Performs other duties as required
Senior Project Coordinator
Project Coordinator
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 • Collaborates in the design, development, and maintenance of study-related web pages, as well as web portal accuracy and consistency• Responsible for the electronic distribution of expedited safety reports, tracking the sent date in CTMS, and filing the project specific email electronically in the Outlook site public folder for the study as well as a hard copy of the email is to be sent to the Novella Clinical Central File Room.• Participates and assists in the planning and creation of client and investigator meetings and related materials • Responsible for printing and forwarding project master file documents to the Novella Clinical Central File Room • Provides other administrative support to senior management, as assigned • Performs other duties, as required
Project Assistant
• 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 • Collaborates in the design, development, and maintenance of study-related web pages, as well as web portal accuracy and consistency• Responsible for the electronic distribution of expedited safety reports, tracking the sent date in CTMS, and filing the project specific email electronically in the Outlook site public folder for the study as well as a hard copy of the email is to be sent to the Novella Clinical Central File Room.• Participates and assists in the planning and creation of client and investigator meetings and related materials • Responsible for printing and forwarding project master file documents to the Novella Clinical Central File Room • Provides other administrative support to senior management, as assigned • Performs other duties, as required
Project Coordination Intern
Meredith Locklear education
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Campbell University
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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