Resultat af søgning: 18 ledige stillinger
...configuration and business processes?
If so, now is your chance to join Ascendis Pharma as our new IT System Manager for the Pharmacovigilance (PV) Product Team in Global IT.
Ascendis Pharma is a fast-growing biopharmaceutical company with locations in Denmark,...
...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
Per the Clinical Monitoring/Site Management Plan (CMP/SMP):
Assesses site processes
Conducts Source...
...Are you passionate about pharmacovigilance and establishing relationships with key partners? Do you have experience in a drug safety environment with pharmacovigilance operational responsibilities and negotiating contracts with strategic partners?
If so, now is your...
...Date: 27 Mar 2024
Location: Ballerup 2750, Denmark, Denmark
Contract type: Permanent
Job ID: 2022
Senior Pharmacovigilance Business Analyst
We are looking for our new Senior Pharmacovigilance Business Analyst
At LEO Pharma, we are on a transformative...
...protecting our tomorrow. We hope that you will share this mission with us. Specialist/ Senior Specialist, Clinical Safety & Pharmacovigilance
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark...
...our best, and authentic is essential to fulfilling our purpose. The Role & Department
A member of the Global Drug Safety & Pharmacovigilance team, focused on safety operations including but not limited to collection of safety information from various sources, SAE...
...Jobbeskrivelse
Placering
Søborg, Denmark Jobkategori
Reg Affairs & Safety Pharmacovigilance
Do you thrive working with project management and would you like to apply great user experience through colour choices and graphic design solutions – while ensuring...
...Responsibilities:
As the Manager for the RA LCM team, you will lead a team of 11 talented and dedicated regulatory affairs and pharmacovigilance specialists, providing guidance and mentorship while fostering a collaborative and knowledge-sharing environment. You will...
...internal audits; responding to inquiries by health authorities, ethics committees, and internal auditors, compliance, Regulatory, Pharmacovigilance (PV) and Medical Affairs
- Responsible and supports development of audit responses and completion of CAPAs.
Collaboration...
...Jobbeskrivelse
Placering
Søborg, Denmark Jobkategori
Reg Affairs & Safety Pharmacovigilance
Do you want to be a part of enabling and supporting the growing product portfolio and life cycle management activities in Novo Nordisk? Would you like to be part...
...in country of residence)
~4+ years relevant experience such as pharmaceutical industry or CRO, in clinical development or pharmacovigilance or significant clinical trial experience as a principal investigator.
~5+ years medical experience as a Dermatologist treating...
...our purpose. QA PV Associate Director
Do you want to safeguard patients and ensure quality compliance in all aspects within Pharmacovigilance? – Then take this great career opportunity!
Are you inspired by working in a company with ambitious goals, exciting...
...Jobbeskrivelse
Placering
Søborg, Denmark Jobkategori
Reg Affairs & Safety Pharmacovigilance
Are you able to cut through complexity and drive regulatory strategies for high-impact projects? Would you like to work together with experts across multiple...
...Jobbeskrivelse
Placering
Søborg, Denmark Jobkategori
Reg Affairs & Safety Pharmacovigilance
We are rapidly expanding our product and project pipeline in Novo Nordisk and are looking for experienced Regulatory Affairs CMC Experts to join RA CMC & Device...
...together with a growing and dynamic quality team take part in the oversight of the compliance, quality, standards, and training for Pharmacovigilance. You will maintain an up-to-date knowledge of regulatory requirements and ensure implementation of these in internal corporate...
...Jobbeskrivelse
Placering
Søborg, Denmark Jobkategori
Reg Affairs & Safety Pharmacovigilance
Are you adept at planning, coordination, problem-solving, and collaboration across the organization? Do you boast experience within clinical trial activities?...
...preferred
~5+ years of previous experience in supporting or participating in FDA or other Health Authorities (HA) related GCP or Pharmacovigilance inspections
~ Previous experience in clinical QA or clinical compliance related functions desired
~ Strong experience in...
...Jobbeskrivelse
Placering
Søborg, Denmark Jobkategori
Reg Affairs & Safety Pharmacovigilance
Do you aspire to accelerate your leadership career within a global pharmaceutical company built on life-changing innovations? Does leading a department of incredibly...
