drug safety

... employment Next Steps: By completing the registration process after clicking on "Apply Now", you will speed up your invitation for an interview. Please note that our central recruiting team is responsible for selecting applicants. They will also call you to arrange an appointment (area code 0211). Health and safety are a top priority for all our activities - even more so in the current situation. We and our clients consult with medical and health experts on an ongoing basis and implement all recommended precautions on our premises to ensure the health of our employees and all other people. Your Contact Adecco Personaldienstleistungen ...

Evotec is a leader in the discovery and development of novel pharmaceuticals with operational sites in Europe and the US. The company has built substantial drug discovery expertise and an industrialized platform that can drive new innovative drugs into the clinic. In addition, Evotec has built a deep internal knowledge-base for the treatment of diseases related to neuroscience, pain, oncology, inflammation, and metabolic diseases. Leveraging these skills and expertise, the company intends to develop best-in-class differentiated therapeutics and deliver superior science-driven discovery alliances with pharmaceutical and biotechnology companies. At our ...

... employment Next Steps: By completing the registration process after clicking on "Apply Now", you will speed up your invitation for an interview. Please note that our central recruiting team is responsible for selecting applicants. They will also call you to arrange an appointment (area code 0211). Health and safety are a top priority for all our activities - even more so in the current situation. We and our clients consult with medical and health experts on an ongoing basis and implement all recommended precautions on our premises to ensure the health of our employees and all other people. Your Contact Adecco Personaldienstleistungen ...

... unmet medical needs and contribute science-based information - Supervise provision of information to the respective disease areas and product-specific training, enabling the sales representatives to understand and convey the scientific benefits of a brand appropriately - Close interactions with Regulatory Affairs and Drug Safety when needed: manage the impact of SAEs and help manage the customer accordingly when SAEs and unexpected AEs arise - Act as Therapeutic Area Consultant for all other departments outside of the medical team including health economy as well as sales and marketing: provide ongoing scientific and medical support - Give ...

... Management and branding - Close collaboration with Product PR and Medical - Close collaboration with sales e.g. communicate and effectively work out new strategies and activities with / for the sales team, train the Sales Force - Recognizing, documenting and reporting of adverse events and technical product complaints to Drug Safety Germany or the responsible service center according to local SOPs Qualifications - Minimum of 3 years of experience in pharma marketing - academic degree (e.g. Master in Science or Economics) - meet local pharma industry requirements Your Personality and Skils: - Strong project management skills - Ability to drive ...

... and clinical data for marketed or developmental client products utilizing scientific resources to deliver impactful presentations in a variety of different settings. - Works collaboratively with client personnel in EMEA/Global Medical Affairs, Clinical Research, Marketing, Market Access, Sales, HEOR, Regulatory Affairs, Drug Safety. - Is responsible for supporting and coordinating Investigator Sponsored Trials in the EMEA region - including collaboration with investigators and internal client personnel and assisting with site selection for clinical trials. - Supports the development of complex clinical data through clinical trials and investigative ...

... based in Noord-Brabant Netherlands. The Company Part of an international organisation, specialising in the production of APIs, Drug Products, and associated Packaging Services. A dedicated professional team ensure the highest standards are pursued at all stages of ... the necessary investigations for commercial and clinical products. Responsibilities - Initiate and own product quality complaints, Safety quality investigations and product security investigations - Perform assessments in support of complaint investigations (e.g. batch record ...

... Senior Drug Safety Associate you will report to the Drug Safety Manager and will be responsible for having an oversight of local Drug Safety and Risk Management related ... activities - data entry of adverse event information into the companys global safety data base - assist E2B submissions to the national competent authority - assist ... event information - assist in overseeing training of new Drug Safety hires as well as non-Drug Safety staff on adverse event report requirements and ... and meetings in agreement with the Drug Safety Manager Your profile: - at least 2 years working experience in Drug Safety / PV - life science degree, registered ...

... products in the local country - Manages all aspects of local individual case safety report (ICSR) Management: - Collecting, recording, processing, translating and ... (where not covered in the global search) for adverse drug reactions, SSRs or other relevant safety data on a weekly basis or according to journal publications - ... - Ensures the PRP is alerted to any safety issues/actions or concerns in a timely manner - Ensures archiving of safety data in accordance with the retention ... background in Pharmacy, Medical or Human Biology Sciences - Understanding of drug safety regulations and obligations - Some experience in the pharmaceutical industry, ...

... academic societies. - Plans and conducts Advisory Boards as needed to obtain insights and advice. - Presents scientific and clinical data in a variety of different settings. - Works collaboratively with personnel in EMEA/Global Medical Affairs, Clinical Research, Marketing, Market Access, Sales, HEOR, Regulatory Affairs, Drug Safety, Public and Patient Affairs. - Supports the generation of scientific data through collaboration with R&D and Clinical Operations, site support in clinical trials and by developing local clinical trials including study protocols. - Is responsible for supporting and coordinating Investigator Sponsored Trials - including ...

The ideal candidate will possess: - Scientific background along with a medico-scientific university degree e.g. Life Science - Pharmaceutical research / drug safety experience in post-marketing environment - Comprehensive knowledge of global safety regulatory requirements and extensive knowledge of safety regulations pertaining to Germany - Working knowledge of European GVP and Regulations pertaining to Adverse Event Reporting - Effective communicator (written and oral); concise, accurate and business appropriate - Proven ability to work cross functionally - Teamwork and initiative - Excellent attention to detail and be able to demonstrate and ...

Responsibilities & key activities - Oprational IIT management according to client and external (legal) requirements - Tracking of IIT progress and filing of all relevant IIT documents (databases, document repositories) - Liaise closely with respective local Medical Affairs Teams, Regulators Affairs, Compliance and Drug Safety - Liaise with Global Medical Affairs Operations group - Establish local SOPs and Working procedures where needed Requirements - Strong interpersonal skills, be a team player and be willing to work in an environment where individual initiative and accountability to the team are required - Effective communicator: interpersonal ...

... Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands.They are a leading organisation in drug development that focuses on Chemistry, Manufacturing and Control (CMC). Role Description You will be part of the team of statisticians, which ... Responsibilities - Create scripts and data files for NONNEM software using SAS - Doing analytical research in clinical trial safety - Oversee all quality regarding data - Identify opportunities and improvements in software modules used - Creating macros to automatize data. ...

... transfer, and commercial supply of biological drug substance and aseptic drug product from CMOs. · Establish supplier strategies and ... make and deliver biologics, meeting established KPIs for safety, quality, customer service, cycle time, and financial targets. - Lead a ... for clinical and commercial manufacturing of drug substance and commercial drug product. - Responsible to align and maintain collaborative ... experience in manufacturing of biologics/vaccines drug substance and aseptic drug product. Demonstrated capability - Multi-disciplinary ...

... Medical Care. freseniusmedicalcare.de Drug Safety Associate (m/w/d) befristet bis 28.02.2022 Innerhalb von ... erhält und aufrechterhält. Als Drug Safety Associate (m/w/d) übernehmen Sie die Registrierung von ... Art (Adverse Event (AE), Adverse Drug Reaction (ADR)) als auch die Eingabe von Arzneimittelrisiken ... Dokumentation von "Periodic Safety Update Report"-bezogenen, sowie fallbezogenen Compliancedaten Sie ... Ebenfalls unterstützen Sie den Drug Safety Manager administrativ bei der Pflege des Pharmacovigilance System Master ... Als Drug Safety Associate (m/w/d) erwarten wir eine abgeschlossene Berufsausbildung zur ...

... Engineer (f/m) 1042 Ihre Aufgaben: - Work on system, subsystem and component/equipment level - Support the Reliability, Availability, Maintainability, Safety (RAMS) project work - Work within technology, budget and schedule with internal and external customers - Perform qualitative Analysis (e.g. FMECA -Failure Mode and ... engineering tasks Ihr Profil: - Experience is necessary for this position - must have experience in RAMS (Reliability, Availability, Maintainability, Safety) project work - Ability to work well in teams and to relate instructions to others in a supportive manner - Ability to work analytically and structured in order to ...

... 0201-279678-20 nutzen Ansprechpartner: Jessica Liel Björn van Andel oder Dich klassisch per E-Mail an: [Apply online] oder [Apply online] bewerben Warte nicht lang - Wir freuen uns auf Dich! Unsere Ansprechpartner für die Organisation der Jobangebote und Stellenausschreibungen im Bereich Security / Sicherheit, Safety sowie Jobs in der Überwachung des Unfallschutzes / Arbeitsschutzes sind in Essen zu erreichen. Weitere Niederlassungen sind Deutschland unter anderem: Magdeburg, Gelsenkirchen, Bochum, Ludwigshafen, Mannheim, Kaiserslautern, Berlin, Eberswalde, Schwedt/Oder, Essen, Köln Keywords: Helfer, Hilfskraft, Security, Werkfeuerwehr, ...

... 0201-279678-20 nutzen Ansprechpartner: Jessica Liel Björn van Andel oder Dich klassisch per E-Mail an: [Apply online] oder [Apply online] bewerben Warte nicht lang - Wir freuen uns auf Dich! Unsere Ansprechpartner für die Organisation der Jobangebote und Stellenausschreibungen im Bereich Security / Sicherheit, Safety sowie Jobs in der Überwachung des Unfallschutzes / Arbeitsschutzes sind in Essen zu erreichen. Weitere Niederlassungen sind Deutschland unter anderem: Magdeburg, Gelsenkirchen, Bochum, Ludwigshafen, Mannheim, Kaiserslautern, Berlin, Eberswalde, Schwedt/Oder, Essen, Köln Keywords: Helfer, Hilfskraft, Security, Werkfeuerwehr, ...