phd pharmacy

A two-year position within pharmaceutical sciences focusing on formulation development and biopharmaceutical understanding of the performance of novel compounds for the treatment of tuberculosis is available at the Department of Physics, Chemistry, and Pharmacy in the pharmacy research group. Starting date: 01 October 2026, or as soon as possible...

A two-year position within pharmaceutical sciences focusing on formulation development and biopharmaceutical understanding of the performance of novel compounds for the treatment of tuberculosis is available at the Department of Physics, Chemistry, and Pharmacy in the pharmacy research group.Starting date: 01 October 2026, or as soon as possible...

A two-year position within pharmaceutical sciences focusing on formulation development and biopharmaceutical understanding of the performance of novel compounds for the treatment of tuberculosis is available at the Department of Physics, Chemistry, and Pharmacy in the pharmacy research group. Starting date: 01 October 2026, or as soon as possible...

DescriptionA two-year position within pharmaceutical sciences focusing on formulation development and biopharmaceutical understanding of the performance of novel compounds for the treatment of tuberculosis is available at the Department of Physics, Chemistry, and Pharmacy in the pharmacy research group.  Starting date: 01 October 2026, or as soon as...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.We are seeking a Senior Clinical Scientist / Clinical...

Are you driven by the challenge of acting as the primary Regulatory Affairs contact between commercial and local regulatory teams? Do you have a strategic mindset and developed stakeholder management skills? The position As the EU Regulatory Affairs Director, you will act as a formal point of Regulatory Affairs (RA) contact for the Head of Commercial...

About the Role Genmab is seeking a Senior CMC Project Manager to join the CMC Life Cycle Management (LCM) Team and support our growing portfolio of commercial products globally. Responsibilities Provide day‑to‑day project management support for commercial manufacturing activities at Genmab’s partnered CMOs, including change controls, deviations and...

Select how often (in days) to receive an alert: Create Alert Global Portfolio Director, Obesity Early Pipeline Category: Commercial Marketing Location: Søborg, Capital Region of Denmark, DK Shape the future of obesity treatment by driving portfolio strategy for one of the most dynamic and high-growth therapy areas in the pharmaceutical industry. Your new...

Shape the future of obesity treatment by driving portfolio strategy for one of the most dynamic and high-growth therapy areas in the pharmaceutical industry.Your new roleAs Global Portfolio Director in Obesity Early Pipeline, you will provide strategic leadership for the future obesity portfolio – from early-stage pipeline projects through to G2 gate...

JobbeskrivelsePlaceringSøborg, DenmarkJobkategoriCommercial MarketingShape the future of obesity treatment by driving portfolio strategy for one of the most dynamic and high-growth therapy areas in the pharmaceutical industry.Your new roleAs Global Portfolio Director in Obesity Early Pipeline, you will provide strategic leadership for the future obesity...

DescriptionTwo full-time postdoc positions are available from 1 November 2026 at the University of Southern Denmark (SDU). One position is a 2-year postdoc within the pharmacoepidemiology group at Clinical Pharmacology, Pharmacy and Environmental Medicine (CPPEM), Department of Public Health. The other is a 2.5-year postdoc within reproductive epidemiology...

We are extra[not]ordinary *(ex· tra· not· or· di· nary |/ ik-ˈstr-not-ȯr-də-ˌner-ē) Adjective: A unique word for Genmab meaning to go way beyond what is usual; to be remarkable; proudly unique and authentic JOB DESCRIPTION At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and...

We are extra[not]ordinary (ex· tra· not· or· di· nary |/ ik-ˈstr-not-ȯr-də-ˌner-ē) Adjective: A unique word for Genmab meaning to go way beyond what is usual; to be remarkable; proudly unique and authentic At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking,...

We are seeking a talented and motivated postdoctoral researcher with a passion for computational peptide design to join an interdisciplinary project developing next‑generation brain‑targeted therapeutics for ischemic stroke. The successful candidate will use de novo design (including in‑house developed methods), molecular modelling and omics‑derived...

Job Summary The Clinical Research Associate role at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field, travel...

Category: Clinical Development Location: Søborg, Capital Region of Denmark, DK Are you passionate about ensuring the safety of patients using pharmaceutical products? Do you want to have a lead role in the Safety Surveillance reporting activities across the Novo Nordisk product portfolio? We are looking for experienced professionals to join us as Safety...

Global Patient Safety Søborg, Denmark Are you passionate about ensuring the safety of patients using pharmaceutical products? Do you want to have a lead role in the Safety Surveillance reporting activities across the Novo Nordisk product portfolio? We are looking for experienced professionals to join us as Safety Medical Writing Principal Specialists to...

Serve as lead writer for high-complexity aggregate safety reports, Risk Management Plans (RMPs), and responses to Health Authority questions of significant strategic importance Act as a key contributor to defining the safety reporting strategy across an entire product portfolio Function as a trusted advisor to cross‑functional stakeholders, influencing...

Safety Surveillance Principal Specialist Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Safety Surveillance Post-Marketing Cardiometabolic III Are you driven by patient safety and scientific excellence? Do you want to influence strategic safety decisions for medicines that can improve the lives of millions...

Global Patient Safety Søborg, DenmarkAre you passionate about ensuring the safety of patients using pharmaceutical products? Do you want to have a lead role in the Safety Surveillance reporting activities across the Novo Nordisk product portfolio? We are looking for experienced professionals to join us as Safety Medical Writing Principal Specialists to join...