Dan Pick Email & Phone Number
@abbvie.com
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Who is Dan Pick? Overview
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Dan Pick is listed as Associate Director: US/Canada Lead - Immunology - Global Regulatory Strategy at AbbVie at AbbVie, based in United States. AeroLeads shows a work email signal at abbvie.com and a matched LinkedIn profile for Dan Pick.
Dan Pick previously worked as Associate Director - Global Regulatory Strategy at Abbvie and Associate Director - Regulatory Affairs Submissions - Clinical Trial Strategy and Submissions Group at Abbvie. Dan Pick holds Bsc (Hons), Applied Microbiology from John Moores University.
Email format at AbbVie
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AeroLeads found 1 current-domain work email signal for Dan Pick. Compare company email patterns before reaching out.
About Dan Pick
An enthusiastic Regulatory Affairs professional with experience gained within Pharmaceutical, Biotechnology and CRO environments, across a range of therapeutic portfolio areas. A proficient worker, independently and as part of a team, in accordance with company and client policies and SOPs. Experienced in providing Regulatory support at both European and Country level, including CTA submission and maintenance, NeeS and eCTD dossier submissions, pre- and post marketing submission activities, and clinical trial supply management.
Listed skills include Regulatory Submissions, Clinical Trials, Regulatory Affairs, Biotechnology, and 23 others.
Dan Pick's current company
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Dan Pick work experience
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Associate Director - Regulatory Affairs Submissions - Clinical Trial Strategy And Submissions Group
Regulatory Affairs Submissions Contractor - Clinical Trial Strategy And Submissions Group
Freelance Regulatory Affairs Consultant
Regulatory Affairs Manager
Working as part of a Global Regulatory team, both in house and on client placements. Personal responsibilities include:Client Regulatory support and project managementSubmission of MAA dossiers in paper, NeeS, and eCTD formatsProject management, submission, and maintenance of Clinical Trial Authorisation (CTA) applications throughout the EUPost-licensing maintenance: submission of variation and renewal packages, revision and preparation of Summary of Product Characteristics (SPCs), labelling, and package leaflets (PILs)Preparation of Clinical- and Non-Clinical Expert Statements for client EU Marketing Authorisation Applications and licence renewalsMerger of two US New Drug Applications (NDAs) into a single dossier in Common Technical Document (CTD) format for a global pharmaceutical companyTransferal of ownership of product licences between affiliates for a global pharmaceutical clientLiaison and communication with competent authoritiesProvision of regulatory support for colleagues on an ad hoc basis
Regulatory Affairs Executive
Preparation of regulatory documentation for European MAAProject management of dossier compilation and submission for a generic product MAA, via the centralised routeEuropean post-approval activities, for example, variationsClient interaction and consultationRegulatory intelligence activities to support the Regulatory Affairs Group
Regulatory Affairs Executive Trainee
Participated in an intensive 6-month Regulatory Affairs training program covering many aspects of Regulatory Affairs procedures, including:Preparation of mock variations, MAA application forms, EudraCT Application forms and quality overview summariesProvided support to senior colleagues for the preparation, review and compilation of a variety of Regulatory submissionsProvide Regulatory intelligence to the Regulatory Affairs Group through preparation of a fortnightly Newsletter containing the latest information from key Regulatory agencies, such as the EMEA, HMA, FDA and MHRA
Clinical Trial Administrator
Set up and maintenance of study records, tracking systems, and trial documentation files in accordance with ICH Good Clinical Practice requirementsOrganisation of investigator meetings and conferencesCoordination of clinical trial supply dispatch and tracking for chain of custodyCentral point of contact within clinical team, ensuring appropriate dissemination of information to team membersLiaison with investigational site staff, customers and subcontractor companiesProduction and distribution of minutes from study teleconferences
Data Entry Clerk
Accurate and timely entry of CRF Data into Clintrial databaseFollow relevant Data Entry Guidelines for each projectRaise data queries relating to logical inconsistencies with the data and refer to Data Manager/Senior Data Entry Clerk as appropriateVisually review Data Listings to CRFFollow all Standard Operating Procedures in place within the department
Molecular Virologist
Research Technician
Laboratory Technician
Dan Pick education
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John Moores University
Frequently asked questions about Dan Pick
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What company does Dan Pick work for?
Dan Pick works for AbbVie.
What is Dan Pick's role at AbbVie?
Dan Pick is listed as Associate Director: US/Canada Lead - Immunology - Global Regulatory Strategy at AbbVie at AbbVie.
What is Dan Pick's email address?
AeroLeads has found 1 work email signal at @abbvie.com for Dan Pick at AbbVie.
Where is Dan Pick based?
Dan Pick is based in United States while working with AbbVie.
What companies has Dan Pick worked for?
Dan Pick has worked for Abbvie, Dsp Regulatory Ltd, Sra Global Clinical Development, Constella Group, and Origin Pharmaceutical Services.
How can I contact Dan Pick?
You can use AeroLeads to view verified contact signals for Dan Pick at AbbVie, including work email, phone, and LinkedIn data when available.
What schools did Dan Pick attend?
Dan Pick holds Bsc (Hons), Applied Microbiology from John Moores University.
What skills is Dan Pick known for?
Dan Pick is listed with skills including Regulatory Submissions, Clinical Trials, Regulatory Affairs, Biotechnology, Oncology, Clinical Research, Pharmaceutical Industry, and Clinical Development.
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