OSLO, Norway, March 11, 2019 - LINK Medical has announced the appointment of
Marie Moores, MSc, as Executive Vice President of Clinical Operations. Marie will join LINK Medical’s
United Kingdom office and support the delivery of international clinical oversight across the
company’s northern European facilities. This appointment represents an important step forwards in
strengthening LINK Medical’s oncology expertise.
Marie Moores joins LINK Medical from a specialist oncology CRO, where she was Director Clinical and
Regulatory Operations for many years. She holds a degree in Clinical Research and has a longstanding
experience in clinical development and regulatory strategy within the field of oncology, advanced
therapies, biologics and gene therapies. She also serves the European Commission in reviewing the
progress of Horizon 2020-funded clinical trials as an external expert.
“By recruiting Marie, we have added significant competence to our leadership team,” said Ola
Gudmundsen, CEO at LINK Medical. “Marie’s impressive experience and knowledge within
international clinical studies and regulatory affairs will greatly strengthen our customer offerings. In
addition, our expansion to the UK broadens our international footprint, enabling stronger service
provision to more companies looking for the LINK Advantage.”
“I am exhilarated to have been offered the opportunity to develop LINK
Medical’s oncology offerings at such an important time for the
organization,” said Marie Moores. “The company’s goals and values are
a perfect match for my next career step, and I am looking forward to
contributing to our future success while delivering the very best service
to our customers.”
About LINK Medical
LINK Medical is a full-service contract research organization (CRO) providing product development
services for the pharmaceutical and medical device industries across Northern Europe. We offer a
well-integrated local presence in the Nordics and Germany. Reaching from early phase development
to post-marketing, we have over 170 employees providing expert guidance across every aspect of a
project – all from ONE source. Our promise is to improve and accelerate your product development
through transformative methods, active communication and optimal solutions. As a strategic
partner, we provide expert competence and technology to enable evidence-based decision-making
that supports the delivery of superior clinical outcomes.
Ola Gudmundsen: CEO, Ola@linkmedical.no
Marie Moores: EVP International Operations, Marie.firstname.lastname@example.org
Read our latest article published in the MVA YEARBOOK. Ola Gudmundsen, our CEO talks about our organic growth and future growth plans as we strengthen key strategic teams. Download PDF or view online publication.
LINK Medical inviterer til åpent møte med innlegg om temaet «Compliance – Hinder eller mulighet?»
Tidspunkt: Tirsdag 9. april 2019 kl. 12-15.
Besøksadresse: LINK Medical Research, Gjerdrums Vei 19, 0484 Oslo. Parkeringsplass rett utenfor.
Påmelding og problemstillinger som ønskes diskutert kan sendes til email@example.com senest 5. april.
Join us on March 7th in Copenhagen at the MVA BOOST seminar 'From Discovery to Clinic: A Comprehensive and Efficient Development Operation' This event will focus on key considerations for transitioning a molecule from discovery through clinical studies. Gunnar Danielsson, our Sr. Regulatory Advisor and former GCP inspector will speak about dive into the subject of different models of clinical studies and their goals as well as the challenges of executing complex clinical studies. This event will for sure be very insightful and educational. Contact us to meet! https://lnkd.in/e6Zrw5K
Mark your calendars and head to Munich to meet us at the OCT next week. You can find us in Booth #10 where you can meet with our dedicated and knowledgeable Medical Device team. We look forward to hearing about your challenges irrespectively of type of product and stage of development.
In September 2018, LINK Medical acquired PCG Clinical Services, located in Uppsala, Sweden. The acquisition allows us to provide you with a richer spectrum of services and expertise, complementing and strengthening our capabilities in key areas such as clinical design, biometrics and medical writing.
Our enhanced offering is available immediately, please contact your local representative to find out more.
Regulatorisk avdeling hos LINK Medical Research AS ekspanderer og er på jakt etter nye medarbeidere. Erfaring fra regulatorisk arbeid eller pharmacovigilance er en fordel, og vi er på jakt etter både deg med kort og lang erfaring. Kandidater uten relevant erfaring med farmasøytisk eller annen naturvitenskapelig bakgrunn er også aktuelle.
Ta kontakt med Grethe Berven, Director Regulatory & Safety, tlf +47 920 25 155 for spørsmål, eller send din CV til firstname.lastname@example.org.»