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Jacob Ekstrøm Email & Phone Number
Principal Consultant and Owner
at
Pharma Native ApS
1 work email found
@varga.dk
LinkedIn matched
✓ Verified Jun 2026
4 data sources
Profile completeness 100%
Current company
Role
Principal Consultant and Owner
Location
Værløse, Capital Region Of Denmark, Denmark
Company size
Who is Jacob Ekstrøm? Overview
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Quick answer
Jacob Ekstrøm is listed as Principal Consultant and Owner at Pharma Native ApS, a company with 1 employees, based in Værløse, Capital Region Of Denmark, Denmark. AeroLeads shows a work email signal at varga.dk and a matched LinkedIn profile for Jacob Ekstrøm.
Jacob Ekstrøm previously worked as Veeva Submissions / Sub Archive Business Support at Ferring Pharmaceuticals and Principal Consultant & Owner at Pharma Native Aps. Jacob Ekstrøm holds Itil® Foundation, Itil Foundation from Service & Support Forum.
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{first}@varga.dk
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Profile bio
About Jacob Ekstrøm
Expert in applying IT within Regulatory Affairs and trimming processes in order to simplify business steps. RIM specialist with experience from multiple RIM implementations. Extensive experience with Data Quality Assessment and Data Governance. Business Process mapping and simplifying project activities. Experience from Document and Data Migration project activities.Passionate RIM Specialist with extensive experience working within Regulatory Affairs and clients.Profound experience with implementation of RIM Systems and aligning with the business.Integrating RIMS solutions with EDMS technologies (Documentum and SharePoint).Extensive RIM Platform knowledge.
Listed skills include Regulatory Affairs, Regulatory Operations, Pharmaceutical Industry, Pharmacovigilance, and 14 others.
Current workplace
Jacob Ekstrøm's current company
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Pharma Native Aps
19 roles
Jacob Ekstrøm work experience
A career timeline built from the work history available for this profile.
Veeva Submissions / Sub Archive Business Support
CurrentE2E Business Process SupportMigration preparationUser Requirements and Configuration Preparation
Sep 2024 - Present
Principal Consultant & Owner
CurrentSelf employed independent Life Science consultant. Process and Software Consulting for Life Sciences.
Aug 2023 - Present
Aug 2023 - Oct 2024
Principal Pharma Consultant
Apr 2022 - Aug 2023
Manager Of Regulatory Applications Services
EpistaLife Science is a team of experts working at the intersection of business priorities and compliance requirements. We are pioneering new methodologies and implementing technologies to help companies balance risk and efficiency to achieve more.We are dedicated to continuously improving compliance and business. By turning compliance obstacles into.
Nov 2018 - Apr 2022
Senior Business Consultant
ISO IDMP business consulting - Structured Substance Information Lead. Aiding the Life Sciences in making qualified decisions based on thorough analysis and assessment work.
Apr 2017 - Oct 2018
Advanced Business Consultant
ISO IDMP business consulting. Life Sciences business consulting within the pharmaceutical industry.
Feb 2015 - Mar 2017
Principal Regulatory Affairs Manager
RIMS Expert - development and maintenance of ALK RIMS (Register) application. Liase with LoB in order to uptimize RIMS usage at ALK.
May 2014 - Jan 2015
Incident And Problem Manager
Leo Pharma A/S
Nov 2013 - Apr 2014
Regulatory Application Professional
Bridging the gap between Regulatory Affairs (business area) and IT (technical area)Providing knowledge about regulatory processes from past experiences to the Regulatory Information Management System project
Jan 2010 - Apr 2014
Regulatory Affairs Manager
Local translations for labellingSubmission management of documentation for National, MRP and CP to local Regulatory Agency (DKMA)Generic competition surveillance
Apr 2008 - Dec 2009
Regulatory Affairs Manager
Stragen Nordic A/S
Managed and coordinated submission of DCP applications for several generic products.
Sep 2007 - Apr 2008
Regulatory Affairs Manager
Local translations for labellingSubmission management of documentation for National, MRP and CP to local Regulatory Agency (DKMA)Generic competition surveillanceLocal pricing submissionsPharmacovigilance back-up
Oct 2006 - Aug 2007
Regulatory Affairs Associate
Local translations for labellingSubmission management of documentation for National, MRP and CP to local Regulatory Agency (DKMA)Generic competition surveillancePharmacovigilance back-upLocal Qualified Person
Mar 2003 - Sep 2006
Regulatory Affairs Associate
Ferrosan A/S
Aug 2002 - Feb 2003
Trainee
Ferrosan A/S
Oct 2001 - Aug 2002
Pharmacist
May 2001 - Sep 2001
Pharmacist
Stengades Apotek, Helsingør
Feb 2000 - Apr 2001
4 education records
Jacob Ekstrøm education
Itil® Foundation, Itil Foundation
Service & Support Forum
Master Of Science, Pharmacy
Danmarks Farmaceutiske Universitet
Master Of Science, Pharmacy
Danmarks Farmaceutiske Universitet
Master Thesis, Pharmacy
FAQ
Frequently asked questions about Jacob Ekstrøm
Quick answers generated from the profile data available on this page.
What company does Jacob Ekstrøm work for?
Jacob Ekstrøm works for Pharma Native ApS.
What is Jacob Ekstrøm's role at Pharma Native ApS?
Jacob Ekstrøm is listed as Principal Consultant and Owner at Pharma Native ApS.
What is Jacob Ekstrøm's email address?
AeroLeads has found 1 work email signal at @varga.dk for Jacob Ekstrøm at Pharma Native ApS.
Where is Jacob Ekstrøm based?
Jacob Ekstrøm is based in Værløse, Capital Region Of Denmark, Denmark while working with Pharma Native ApS.
What companies has Jacob Ekstrøm worked for?
Jacob Ekstrøm has worked for Pharma Native Aps, Ferring Pharmaceuticals, Pharma It, Epista Life Science, and Nnit.
How can I contact Jacob Ekstrøm?
You can use AeroLeads to view verified contact signals for Jacob Ekstrøm at Pharma Native ApS, including work email, phone, and LinkedIn data when available.
What schools did Jacob Ekstrøm attend?
Jacob Ekstrøm holds Itil® Foundation, Itil Foundation from Service & Support Forum.
What skills is Jacob Ekstrøm known for?
Jacob Ekstrøm is listed with skills including Regulatory Affairs, Regulatory Operations, Pharmaceutical Industry, Pharmacovigilance, Regulatory Submissions, Regulatory Requirements, Training, and Employee Training.
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