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9 Jobs für Pharmacovigilance Associate


Stellenangebote Pharmacovigilance Associate Jobs


Job am 02.03.2026 bei Mindmatch.ai gefunden Syneos Health

CRA single sponsor-Germany

• AT- 9 Wien [. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT[...] deviation/ violations and pharmacovigilance issues. For the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and [. .. ] oversight of the Lead CRA, to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA) . Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ]

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Job am 22.02.2026 bei Mindmatch.ai gefunden Syneos Health, Inc.

CRA Germany or Austria-single-client

• AT- 9 Wien [. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project [. .. ]

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Job am 22.02.2026 bei Mindmatch.ai gefunden Syneos Health, Inc. CRA single sponsor-Germany • AT- 9 Wien [. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

Business Consultant-R D (Remote)

• Berlin Beratungs-/ Consultingtätigkeiten [. .. ] of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy Operations as well as Quality [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and Safety (eg. Pharmacovigilance) . As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R D planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through facetoface discussions, workshops, email, etc. ) to deliver demonstrable, [. .. ] faced by the customer Be a primary client contact for operational project questions, developing the relationship through facetoface discussions, workshops, phone, and email contact Manage the work and priorities of Associate Consultants in your workstream Support and mentor Associates in developing skills and professional capabilities Build trusted relationships with customer stakeholders Bring to your customers a good level of industry/ market/ functional insights Input into business development opportunities and proposals Help develop and disseminate thought leadership Requirements Bachelors or Masters degree [. .. ]

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Job am 02.03.2026 bei Jobleads gefunden

Associate Director, Medical Affairs Amyloidosis

• München, Bayern Führungs-/ Leitungspositionen [. .. ] the development of a deep understanding of the respective indication area. Acquisition of sufficient knowledge of current local regulations of the pharmaceutical industry and collaboration with the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Regulatory Affairs department, Pharmacovigilance department, Quality Assurance, Legal, Commercial Department and all other company divisions. You Will Need To Have University degree in medicine (preferred) , pharmacy, or biology, Ph D desirable 5-8 years of experience in the pharmaceutical/ biotechnology industry in medical affairs Strong leadership skills and the ability to motivate teams Proven [. .. ]

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Job am 20.11.2025 bei Jobleads gefunden

Manager (w/m/d) Regulatory Affairs Biocides

• Köln, Nordrhein- Westfalen [. .. ] Menschen an und setzen uns dafür ein, unsere Mitarbeitenden bei der Entwicklung ihres individuellen Potenzials zu unterstützen. Bitte richten Sie Ihre Bewerbung an das Recruiting Team. Seniority [...]
MEHR INFOS ZUM STELLENANGEBOT[...] level Seniority level Associate Employment type Employment type Full-time Job function Job function Other Industries Chemical Manufacturing Referrals increase your chances of interviewing at LANXESS by 2x Get notified about new Manager (w/m/d) Regulatory Affairs Biocides jobs in Cologne, North Rhine-Westphalia, Germany. Cologne, North Rhine-Westphalia, Germany 3 weeks ago [. .. ] ago Cologne, North Rhine-Westphalia, Germany 2 weeks ago Regulatory Affairs-Labelling Specialist (w/m/d) Langenfeld, North Rhine-Westphalia, Germany 2 weeks ago Global ICT Business Partner (Regulatory Affairs Pharmacovigilance) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 70115425 [. .. ]

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Job am 14.10.2025 bei Jobleads gefunden

Projektmitarbeiter der Geschäftsführung (m/w/d) Vollzeit in München

• München, Bayern Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium Betriebliche Altersvorsorge [. .. ] type Full-time Job function Job function Project Management Industries Professional Services Referrals increase your chances of interviewing at BONAGO Incentive Marketing Group by 2x Get notified about [...]
MEHR INFOS ZUM STELLENANGEBOT[...] new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Tester for a car voice assistant project-English (Australian) speaker Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Supply Chain Project Coordinator (m/f/d) Product Process Support Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Junior Projektmanager Elektrotechnik (all gender) Working Student Smart Site Operations Strategy (m/f/d) Intern Sustainability Management [. .. ]

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Job am 01.03.2026 bei Neuvoo gefunden Alexion Pharmaceuticals Associate Director, Medical Affairs Amyloidosis • Munich, Bavaria Führungs-/ Leitungspositionen [. .. ] the development of a deep understanding of the respective indication area. Acquisition of sufficient knowledge of current local regulations of the pharmaceutical industry and collaboration with the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Regulatory Affairs department, Pharmacovigilance department, Quality Assurance, Legal, Commercial Department and all other company divisions You will need to have: University degree in medicine (preferred) , pharmacy, or biology, Ph D desirable 5-8 years of experience in the pharmaceutical/ biotechnology industry in medical affairs Strong leadership skills and the ability to motivate teams Proven [. .. ]

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Job am 24.01.2026 bei Neuvoo gefunden Parexel

Associate Medical Director/ Study Physician-Oncology trials-FSP-Remote

• Berlin Führungs-/ Leitungspositionen [. .. ] of 4 years of active clinical practice experience; specialization in internal medicine or general practice is desirable. Experience in pharma industry or CRO in medical or project [...]
MEHR INFOS ZUM STELLENANGEBOT[...] management or global pharmacovigilance functions/ any other relevant medical function ideally in Clinical Development is desirable. Understanding of relevant regulations and guidance including ICH-GCP. Ideally experienced with data visualization systems and IT systems. Clinical development/ trials experience which would be an additional asset 77820497 [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Pharmacovigilance Associate pro Jahr?

Als Pharmacovigilance Associate verdient man zwischen EUR 50.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Pharmacovigilance Associate Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Pharmacovigilance Associate Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Associate Jobs?

Aktuell suchen 5 Unternehmen nach Bewerbern für Pharmacovigilance Associate Jobs.


Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Associate Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Associate Stellenangebote:


  • Syneos Health (1 Job)
  • Alexion Pharmaceuticals (1 Job)
  • Parexel (1 Job)


In welchen Bundesländern werden die meisten Pharmacovigilance Associate Jobs angeboten?

Die meisten Stellenanzeigen für Pharmacovigilance Associate Jobs werden derzeit in Berlin (2 Jobs), Bayern (2 Jobs) und Nordrhein-Westfalen (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Pharmacovigilance Associate Jobs?

Pharmacovigilance Associate Jobs gehören zum Berufsfeld Pharmazie.


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