23 Jobs für Pharmacovigilance Associate
Stellenangebote Pharmacovigilance Associate Jobs
Job vor 4 Tagen bei Jooble gefunden
• München
[. .. ] 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 via review of site source documents and medical records Applies [. .. ] 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 project-specific 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 and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Project Manager
• München
[. .. ] and FDA regulations and within established timelines. Serves as study lead and primary contact for sponsors. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data management, biostatistics, pharmacovigilance, and central laboratory. Generates and presents frequent study status updates and reports to sponsor. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Supervises and trains Associate PMs. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones. Ensures accuracy of reports and material work product. Provides monthly billing information [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
[. .. ] 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 project-specific 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 [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
[. .. ] 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 via review of site source documents and medical records Applies [. .. ] 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 project-specific 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 and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
[. .. ] the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
[. .. ] 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 project-specific 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 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
[. .. ] the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
CRA-single sponsor-Germany
• München
[. .. ] 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 project-specific 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 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
[. .. ] the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor (m/w/d)
• München
[. .. ] the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
[. .. ] the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Associate Director Quality Assurance (hybrid in Europe-onsite when needed for audits and inspe. . .
Führungs-/ Leitungspositionen
Work-Life-Balance
Overview We are Prime Vigilance (part of Ergomed Group) , a specialised mid-size
pharmacovigilance service provider established in 2008. We cover services within: Medical Information, Pharmacovigilance, Regulatory Affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Quality Assurance. Prime Vigilance provides first class support to our pharmaceutical and biotechnology partners, maintaining long lasting relationships and covering all therapy areas including medical device. We invest in staff with training and development, value [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Baden- Württemberg
Führungs-/ Leitungspositionen
Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, Germany, or relocation to Germany (relocation assistance available) . #clientvacancy #director #pv oncology Together with a German member of INRALS [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (International Network of Recruitment Agencies in Life Sciences) , we are looking for an Associate Director Patient [. .. ] for the therapeutic area Oncology. Client : One Of the Worlds 20 Leading (Bio) Pharmaceutical Companies 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 with the clinical development department and will be involved in a very strategic and global function. TASKS RESPONSIBILITIES: Crafting proactive, patient-centric RM strategies tailored to designated compounds. Overseeing and [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Associate Medical Director Study Physician Oncology trials FSP
• 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. Key Skills EMR Systems Post Residency Experience Occupational Health Experience [. .. ]
Job gestern bei Jobleads gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München, Bayern
[. .. ] 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 via review of site source documents and medical records [. .. ] 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 project-specific 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 and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Associate Director-(Senior) Patient Safety Physician (gn) : Inflammation Baden-Württemberg, Ge. . .
• Baden- Württemberg
Führungs-/ Leitungspositionen
Associate Director-(Senior) Patient Safety Physician (gn) : Inflammation Baden-Württemberg, Germany, or relocation to Germany (relocation assistance available) . #clientvacancy #director #pv Together with a German member of INRALS (International [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Network of Recruitment Agencies in Life Sciences) , we are looking for an Associate Director Patient Safety [. .. ] for the therapeutic area Inflammation. Client : One Of the Worlds 20 Leading (Bio) Pharmaceutical Companies 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 with the clinical development department and will be involved in a very strategic and global function. TASKS RESPONSIBILITIES: Crafting proactive, patient-centric RM strategies tailored to designated compounds. Overseeing and [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
• Berlin
[. .. ] support our customers to deliver on their complex business challenges. As part of the team, you will focus on one or more critical areas such as Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development, Regulatory Affairs, Pharmacovigilance/ Drug Safety, and Quality Management. What Youll Do Lead multiple project engagement teams empowering the team to plan and manage all aspects of delivery, from scope to quality assurance Be responsible for the end-to-end design, build, and delivery of deliverables that meet overall project goals and objectives Proactively [. .. ] your chances of interviewing at Veeva Systems by 2x Customer Success Manager-Agencies (m/f/d) Engineering Manager-Public Cloud, Python, Golang Software Engineering Manager-Desktop and Embedded Linux Optimisation Associate Event Project Manager (based in Germany) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 77870955 [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Drug Safety Associate Freelance
• Mainz, Rheinland- Pfalz
Freiberuflich
[. .. ] (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Freelance Drug Safety Associate handles drug safety and pharmacovigilance activities in accordance with TFS/ client SOPs and regulatory requirements. The role provides flexible, on-demand expertise to ensure accurate collection, assessment, coding, and documentation of safety data. Key Responsibilities Manage the handling, collection, assessment, and entry of SAEs, AEs, spontaneous reports, related activities in compliance with SOPs and regulatory [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
• 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 [. .. ]
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 [. .. ]
Job am 05.09.2025 bei Jobleads gefunden
Business Consultant-R D (Remote)
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 and Safety [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (e. g. , 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 face-to-face discussions, workshops, email, etc. ) to [. .. ] the customer Be a primary client contact for operational project questions, developing the relationship through face-to-face 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 Qualifications Bachelor s or Masters [. .. ]
Job am 28.08.2025 bei Jobleads gefunden
Projektmitarbeiter der Geschäftsführung (all genders) Vollzeit in München
• München, Bayern
Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium
[. .. ] type Full-time Job function Job function Project Management Industries Software Development 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) Tester for a car voice assistant project-English (Australian) speaker Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Supply Chain Project Coordinator (m/f/d) Product Process Support Greater Munich Metropolitan Area 4 weeks ago Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Hallbergmoos, Bavaria, Germany 1 month ago Client Success Project Business Coordinator (m/f/x) Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Working Student Smart Site Operations [. .. ]
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 [. .. ]
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 23 offene Stellenanzeigen für Pharmacovigilance Associate Jobs.
In welchen Bundesländern werden die meisten Pharmacovigilance Associate Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Associate Jobs werden derzeit in Berlin (4 Jobs), Bayern (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Associate Jobs?
Pharmacovigilance Associate Jobs gehören zum Berufsfeld Pharmazie.
