Associate Director Pharmacovigilance Operations
Aachen
Home Office
PAION Pharma GmbH
… set-up of PhV processes. Knowledge of PhV requirements and legislation for drug development, regional PhV experience. Experience in using a defined … Your tasks About the role: The Associate Director Pharmacovigilance Operations is responsible for ensuring that all … Operations is responsible for ensuring that all aspects of safety reporting in relation to PAION (both marketed and in development) products …Drug Safety Stellenangebote
Clinical Research Associate, sponsor dedicated
Home Office
Vollzeit
ICON
… and guidelines Coordinate timely shipment of clinical supplies and study drug to sites in collaboration with regional CRAs Maintain adequate site … The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main … open issue resolution, work on recruitment strategies, and monitor safety at the site. The CRA will conduct site qualification visits as assigned, …Drug SafetyAssociate Director Pharmacovigilance Operations (part-time)
Aachen
Home Office
PAION Pharma GmbH
… set-up of PhV processes. Knowledge of PhV requirements and legislation for drug development, regional PhV experience. Experience in using a defined … Your tasks About the role: The Associate Director Pharmacovigilance Operations is responsible for ensuring that all … Operations is responsible for ensuring that all aspects of safety reporting in relation to PAION (both marketed and in development) products …Drug Stellenangebote
Clinical Research Coordinator I
Hamburg
Vollzeit
Velocity Clinical Research, Inc.
… population for each assigned protocol. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab … degree with 1 year of relevant experience in the life science industry OR Associate’s degree with 2 years of relevant experience in the life science industry … information and Velocity confidential information Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse …Drug Safety AssociateAssociate Specialist, Clinical Research (m/f/d)
Schwabenheim
Vollzeit
MSD
… and expedite clinical studies on products that have investigational new drug or medical devices approval. Responsible for reviewing adverse event cases … our Schwabenheim location, we are looking for you as a Clinical Research Associate (m/f/d), starting immediately, for a fixed-term period of 2 years and on a … Research team is responsible for clinical studies to demonstrate the safety and efficacy of new drugs, and new indications for products already on the …Drug Safety AssociateDrug Safety Associate (m/w/d)
Bad Homburg vor der Höhe
Ausbildung
Fresenius Medical Care
… von Arzneimittelrisiken medizinischer Art (Adverse Event (AE), Adverse Drug Reaction (ADR)) als auch die Eingabe von Arzneimittelrisiken medizinischer … Als „Drug Safety Associate (m/w/d)" übernehmen Sie die Registrierung von Arzneimittelrisiken … Als „Drug Safety Associate (m/w/d)" übernehmen Sie die Registrierung von …Safety AssociateAssociate Director Real World Evidence (Oncology) all genders/part-time/full-time
Darmstadt
Vollzeit
Merck KGaA
… and Data (RWE/D) strategy and studies, with a particular focus on early drug development and integrated evidence planning. You will provide scientific … or drug-specific RWE studies, encompassing regulatory grade studies, i.e. safety related studies, external control arm studies and natural history of …Drug Safety AssociateClinical Research Coordinator II
Wiesbaden
Vollzeit
Velocity Clinical Research, Inc.
… and in preparation for monitor visits. Perform clinical duties (e.g., drug preparation and administration, fibroscan, phlebotomy, ECG,lab processing) … degree and 2 years relevant experience in the life science industry OR Associate’s degree with 4 years relevant experience in the life science industry OR … and Velocity confidential information Verify and escalate patient safety concerns by ensuring all adverse events, serious adverseevents, and …Safety Associate StellenangeboteClinical Research Coordinator I
Leipzig
Vollzeit
Velocity Clinical Research, Inc.
… population for each assigned protocol. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab … degree with 1 year of relevant experience in the life science industry OR Associate’s degree with 2 years of relevant experience in the life science industry … information and Velocity confidential information Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse …Drug AssociateClinical Research Coordinator II
Wiesbaden
Vollzeit
Velocity Clinical Research, Inc.
… and in preparation for monitor visits. Perform clinical duties (e.g., drug preparation and administration, fibroscan, phlebotomy, ECG,lab processing) … degree and 2 years relevant experience in the life science industry OR Associate’s degree with 4 years relevant experience in the life science industry OR … and Velocity confidential information Verify and escalate patient safety concerns by ensuring all adverse events, serious adverseevents, and …Drug AssociateClinical Program Lead
Biberach an der Riß
Vollzeit
BI International GmbH
… Company Core Data Sheet, Annual Safety Report / IND (Investigational New Drug) Safety Reports. Thanks to your expertise, you provide medical leadership … you review and approve publications within your project in collaboration associate Head of Medicine. As a Senior Clinical Program Leader, you: You author … Brochure, medical input to the Company Core Data sheet, Annual Safety Report / IND Safety Reports, preparation for the Milestones Start of …Safety StellenangeboteClinical Research Coordinator I
Hamburg
Vollzeit
Velocity Clinical Research, Inc.
… population for each assigned protocol. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab … degree with 1 year of relevant experience in the life science industry OR Associate’s degree with 2 years of relevant experience in the life science industry … information and Velocity confidential information Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse …Safety Stellenangebote(Associate) Director* Non-Clinical Safety & DMPK
Mainz
Vollzeit
BioNTech AG
… different stages of pharmaceutical development by implementing strategic drug metabolism and pharmacokinetics (DMPK) paths. BioNTech is expanding its … for a healthy future in many people's lives. Senior DMPK Scientist* as (Associate) Director* Non-Clinical Safety & DMPK At BioNTech, you will contribute to … lives. Senior DMPK Scientist* as (Associate) Director* Non-Clinical Safety & DMPK At BioNTech, you will contribute to non-clinical development and …Safety AssociateSenior Associate Medical Affairs CE
Kreis Neuss
Vollzeit
Kenvue
… area of Johnson & Johnson OTC drugs. Closely cooperates with the drug regulatory affairs, quality department and marketing and sales departments … Description Kenvue is currently recruiting for: Senior Associate Medical Affairs CE This position reports into the Senior Associate Manager … use of medicines, their pharmaceutical quality, effectiveness, and safety. Answers inquiries from practicing pharmacists and hospital pharmacists …Drug Associate