Pharmacovigilance Specialist Stellenangebote

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Stellenangebote Pharmacovigilance Specialist Jobs bei Neuvoo

Job vom 02.12.2024 Mag. Monika Kail

PV/ QA Specialist (f/m/d)

• Vienna, Austria Homeoffice möglich

MEHR

[...] sized pharmaceutical wholesaler based in the city centre of Vienna who distributes pharmaceutical products and medical devices within the European Union and in several countries outside the EU. The company is currently offering a fulltime position for a PV/ QA Specialist (f/m/d) 38, 5 hours per week, hybrid, Vienna This coordinative role is part of a small cross functional and highly [...] the companys business partners. Supporting the Quality Manager in various Quality Assurance tasks like the preparation of documents, the creation of SOPs, support during Audits, etc. Having some years of working experience in Pharma/ Biotech Industry in the field of Pharmacovigilance is necessary. Experience in Materiovigilance would be great. Having a good understanding of Quality Management Systems and GDP. Being fluent [...]
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Stellenangebote Pharmacovigilance Specialist Jobs bei Jobleads

Job vom 28.11.2024

Vice President- Research Development

Führungs-/ Leitungspositionen

MEHR

[...] development plans with milestones to achieve technical, development regulatory objectives. Established R D track record, credibility and reputation in cancer therapeutics and/ or diagnostics including relevant publications, grants and fundraising How to Apply Click apply or contact Jo Turner, Senior Specialist Consultant on 03 9938 7120 for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group recruits all positions: executive, permanent, contracting/ temp, at all levels, across all areas of healthcare- Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care. Medical Affairs Life Sciences Recruitment - Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific Commercial Recruitment - Marketing, Sales, Analytics, Government and External Affairs Business Operations Infrastructure Recruitment [...]

Job vom 23.11.2024

Specialist, Pharmacovigilance

• Mannheim, Baden- Württemberg

MEHR

[...] challenges and opportunities? Then, Pharmalex is your career opportunity. Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, market development, and effective product maintenance. Specialist, Pharmacovigilance Your Job Management of safety- related information from all sources (incl. but not limited to spontaneous, literature, clinical studies, medical [...]
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Job vom 08.11.2024

Data Analytics Senior Specialist (m/f/x)

• München, Bayern

MEHR

Select how often (in days) to receive an alert: Data Analytics Senior Specialist (m/f/x) Passion for Innovation. Compassion for Patients. With over 120 years of experience and more than 17, 000 employees in [...] Canada. For Daiichi Sankyo Europe GmbH in Munich we are looking for a qualified Data Analytics Senior Specialist (m/f/x) Purpose of the function: As Systems Manager Senior Specialist in the Database Management and Analytics (DBMA) team within Clinical Safety and Pharmacovigilance (CSPV) , you will focus on data analysis and global adverse event monitoring using Oracle Argus and other data sources. [...]

Job vom 04.11.2024

Director- (Senior) Patient Safety Physician (gn) : Psychiatry

Führungs-/ Leitungspositionen

MEHR

[...] DAS UNTERNEHMEN For a globally leading (bio) pharmaceutical company, we are assigned to recruit a Director Patient Safety (gn) for the therapeutic area Psychiatry and CNS. Your primary focus will revolve around orchestrating the global initiatives for Patient Safety and Pharmacovigilance (PSPV) and Risk Management (RM) pertaining to compounds at various stages of development. In this role, you will work closely [...] scientific insights into regulatory documents, including PSURs, DSURs, RMPs, and Clinical Overview Statements. Chair multidisciplinary Benefit Risk Teams. Keeping senior management apprised of the safety profile of designated drugs and suggesting PV/ RM actions. IHR PROFIL Medical degree (ideally with specialist education in psychiatry) with clinical and/ or clinical research experience in the according therapeutic area. Proficient knowledge in pharmacovigilance (PV) [...]
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Weitere Stellenangebote Pharmacovigilance Specialist bei Neuvoo

Stellenangebot Pharmacovigilance Specialist Job bei Wörwag Pharma

Job vom 20.11.2024 Wörwag Pharma

Specialist Medical Writing Advice (m/f/x)

• Böblingen, Baden- Württemberg Work-Life-Balance

MEHR

[...] is an expression of our colorful corporate culture and our collegial cooperation among our now 1, 200 employees worldwide. Become a part of our team in our headquarter in Böblingen (near Stuttgart) because we are looking for you as a Specialist Medical Writing and Advice (m/w/d) These tasks await you Collaboration for preparation of parts of eCTD dossiers which are relevant [...] evaluation of the accuracy, consistency, and plausibility of externally produced clinical and non- clinical documents which are relevant for marketing authorisation Review and evaluation of information texts for medicinal products and food supplements Interface/ support of Regulatory Affairs and Global Pharmacovigilance in medical/ scientific issues Editing/ review of technical information and directions for use with regard to medico- scientifically relevant passages, [...]

Stellenangebot Pharmacovigilance Specialist Job bei Miltenyi Biomedicine

Job vom 13.11.2024 Miltenyi Biomedicine

Global Regulatory Affairs Manager- ATMP (m f d)

• Bergisch Gladbach, North Rhine- Westphalia

MEHR

[...] planning in line with the global regulatory strategy. Working closely with health authorities to coordinate, communicate and manage all regulatory interactions is another essential part of this position. You will also contribute relevant aspects of product safety and quality regarding pharmacovigilance and regulatory requirements. Managing the development and maintenance of prescribing information and risk management plans completes the diverse range of [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, sport, and [...]

Stellenangebot Pharmacovigilance Specialist Job bei Chiesi Group

Job vom 14.08.2024 Chiesi Group

Specialist Regulatory Affairs Pharmacovigilance (all genders)

• Hamburg Abgeschlossenes Studium Abgeschlossene Ausbildung Flexible Arbeitszeiten

MEHR

Specialist Regulatory Affairs Pharmacovigilance (all genders) Abteilung: Pharmaceutical Affairs Team: R D, Pharmacovigilance Regulatory Affairs Stellentyp: Direkter Mitarbeiter Vertragsart: Vorübergehend Standort: Hamburg, DE Über [...]

Job vom 28.06.2024 Miltenyi Biomedicine

Manager- Global Regulatory Affairs- ATMP (m f d)

• Bergisch Gladbach, North Rhine- Westphalia

MEHR

[...] planning in line with the global regulatory strategy. Working closely with health authorities to coordinate, communicate and manage all regulatory interactions is another essential part of this position. You will also oversee relevant aspects of product safety and quality regarding pharmacovigilance and regulatory requirements. Leading the development and maintenance of prescribing information and risk management plans completes the diverse range of [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, sport, and [...]

Stellenangebot Pharmacovigilance Specialist Job bei Pro Pharma Group

Job vom 27.06.2024 Pro Pharma Group

Multilingual Medical Information Specialist- Norwegian Speaking

MEHR

[...] therapies. As the world s largest RCO (Research Consulting Organization) , Pro Pharma partners with its clients through an advise- build- operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality compliance, pharmacovigilance, medical information, and R D technology, Pro Pharma offers an end- to- end suite of fully customizable consulting solutions that de- risk and accelerate our partners most high- profile drug and device programs. We re looking for a Multilingual Medical Information Specialist to join our Medical Information Department. You will be responsible for providing a high- quality Medical Information service via phone [...]

Stellenangebot Pharmacovigilance Specialist Job bei Bio Marin

Job vom 26.06.2024 Bio Marin Temporary Territory Manager, Germany

MEHR

[...] of the organization. The willingness to travel up to 70 of the working hours is expected. EDUCATIONBS/ BA degree in life sciences or business with pharmaceutical sales representative education Sales- experience in innovative product- areas, preferred for hospital drugs in specialist indications EXPERIENCE Work experience in commercial and marketing for pharmaceutical and/ or biotechnology company Good skills in English as well as effective communication skills in the local language Computer competency in Power Point, Microsoft Word and Excel Familiarity with basic regulatory requirements, particularly sales and marketing activities as well as pharmacovigilance Good understanding of Health Care Systems including financing and public health policy Flexible, dedicated, ability to recognize customers needs, open [...]
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Stellenangebote Pharmacovigilance Specialist Jobs bei NewScientist Jobs

Job vom 30.11.2024 Jazz Pharmaceutical Senior Clinical Quality Assurance Specialist • United Kingdom

MEHR

[...] of all participants in drug development activities on behalf of the company. To understand and apply appropriate guidelines and regulations, including ICH, FDA, MHRA and EMA and other worldwide regulations, in a risk- based manner to Clinical Studies/ Trials, including Pharmacovigilance activities and quality vendor management. CQA Quality Lead for Clinical Quality Assurance to support Study teams, providing quality support and [...]

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