16 Jobs für Pharmacovigilance Associate
Stellenangebote Pharmacovigilance Associate Jobs
Job vor 12 Tagen bei Mindmatch.ai gefunden
Amgen Inc. (IR)
• AT- 2 Lavamünd
Amgen seeks a Senior
Associate Global Safety (Local Safety Switzerland) based in Rotkreuz to support local
pharmacovigilance activities and provide safety expertise to the local business. You will collaborate with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] German and Austrian teams, manage safety data processing, and ensure Swiss regulatory compliance within Amgens safety framework. You will contribute to safety reporting, audits, and inspections, while training staff and aligning PV requirements across affiliates. J-18808-[. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Swiss Local Safety Pharmacovigilance Associate
• Lavamünd, Kärnten
Amgen seeks a Senior
Associate Global Safety (Local Safety Switzerland) based in Rotkreuz to support local
pharmacovigilance activities and provide safety expertise to the local business. You will collaborate with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] German and Austrian teams, manage safety data processing, and ensure Swiss regulatory compliance within Amgens safety framework. You will contribute to safety reporting, audits, and inspections, while training staff and aligning PV requirements across affiliates. #J-[. .. ]
Job gestern bei Mindmatch.ai gefunden
Jobgether
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
Jobgether is seeking an
Associate Director, Medical Affairs on behalf of a partner company. This role is remote with travel up to 20 for congresses and external engagements, and you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will lead medical affairs activities across thought leader engagement, scientific communications, publications, and literature surveillance. You will translate clinical evidence into strategic recommendations, build relationships with key thought leaders, plan scientific exchanges, and support pharmacovigilance and J-18808-Ljbffr 03498761 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Planet Pharma
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
We are seeking an experienced and highly motivated
Associate Director, Clinical Biomarker Biostatistics to play a pivotal role in advancing our clinical development and precision medicine strategies. This is an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] exciting opportunity for a strategic and handson biostatistician to drive the statistical leadership of biomarker initiatives across a diverse clinical portfolio. As a key member of the Biometrics organization, [. .. ] 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. J-18808-Ljbffr 03446195 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Revolution Medicines
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] urgency and hold ourselves to a high standard of rigorall in service of patients. The Opportunity: As part of our expanding European organization, we seek a strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and hands-on Associate Director, Regulatory Affairs, Europe who will provide regulatory leadership for designated programs at Rev Med. The candidate will be responsible for the preparation end-to-end execution of regulatory MAA filings across the EU, EEA, UK and Switzerland for oncology programs, ensuring alignment of the European regulatory strategy with the [. .. ] global and regional regulatory strategies. Act as a strategic partner to cross-functional teams, including R D, Medical Affairs, Safety, Market Access, and Commercial. Ensure compliance with applicable European regulatory, pharmacovigilance, and governance requirements. Monitor and interpret evolving European regulatory requirements, guidelines, and trends, and communicate their impact across functions. Oversee external vendors and CROs to ensure timely, high-quality regulatory submissions and approvals. Required Skills, Experience and Education: Degree in biological or life sciences, pharmacy, medicine, or related fields. An [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Amgen Inc. (IR)
• AT- 2 Lavamünd
[. .. ] collaborators who achieve togetherresearching, manufacturing and delivering ever-better products that read over 10 million patients worldwide. Its time for a career you can be proud of. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us. SENIOR ASSOCIATE GLOBAL SAFETY (LOCAL SAFETY SWITZERLAND) LIVE What you will do In this vital role as a Senior Associate Global Safety (Local Safety Switzerland) you will support local pharmacovigilance activities in Switzerland and support provision of safety expertise to the local business. You will conduct core safety activities including data collection, processing, distribution and regulatory submission, based on appropriate training and assigned roles within the safety database and related systems. You will maintain compliance with Swiss legislation, Amgen policies [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
[. .. ] protecting the confidentiality of each subject/ patient. Assess 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 project 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, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ]
Job gestern bei Jobleads gefunden
Senior Associate Director, Medical Affairs (Remote)
• Lavamünd, Kärnten Lavamuend
Führungs-/ Leitungspositionen
Jobgether is seeking an
Associate Director, Medical Affairs on behalf of a partner company. This role is remote with travel up to 20 for congresses and external engagements, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will lead medical affairs activities across thought leader engagement, scientific communications, publications, and literature surveillance. You will translate clinical evidence into strategic recommendations, build relationships with key thought leaders, plan scientific exchanges, and support pharmacovigilance and #J-18808-Ljbffr 03493143 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director, Regulatory Affairs, Europe
• Lavamünd, Kärnten Lavamuend
Führungs-/ Leitungspositionen
[. .. ] urgency and hold ourselves to a high standard of rigorall in service of patients. The Opportunity: As part of our expanding European organization, we seek a strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and hands-on Associate Director, Regulatory Affairs, Europe who will provide regulatory leadership for designated programs at Rev Med. The candidate will be responsible for the preparation end-to-end execution of regulatory MAA filings across the EU, EEA, UK and Switzerland for oncology programs, ensuring alignment of the European regulatory strategy with the [. .. ] global and regional regulatory strategies. Act as a strategic partner to cross-functional teams, including R D, Medical Affairs, Safety, Market Access, and Commercial. Ensure compliance with applicable European regulatory, pharmacovigilance, and governance requirements. Monitor and interpret evolving European regulatory requirements, guidelines, and trends, and communicate their impact across functions. Oversee external vendors and CROs to ensure timely, high-quality regulatory submissions and approvals. Required Skills, Experience and Education: Degree in biological or life sciences, pharmacy, medicine, or related fields. An [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director Biostatistics
• Lavamünd, Kärnten Lavamuend
Führungs-/ Leitungspositionen
We are seeking an experienced and highly motivated
Associate Director, Clinical Biomarker Biostatistics to play a pivotal role in advancing our clinical development and precision medicine strategies. This is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an exciting opportunity for a strategic and handson biostatistician to drive the statistical leadership of biomarker initiatives across a diverse clinical portfolio. As a key member of the Biometrics organization, [. .. ] 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. #J-18808-Ljbffr 03438143 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate-Berlin/ Leipzig/ Dresden
Clinical Research
Associate-Berlin/ Leipzig/ Dresden Updated: Yesterday Location: Remote, Germany Job ID: 25112473 Description Clinical Research Associate-Berlin/ Leipzig/ Dresden Syneos Health is a leading fully-integrated life sciences services organization [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them [. .. ] 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 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 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate Multi-Sponsor
[. .. ] Communicate and escape serious issues to the project team and develop action plans Verify informed consent processes and documentation Assess subject/ patient safety, clinical data integrity, protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviations/ violations and pharmacovigilance issues Assess site processes and conduct source document review of site source documents and medical records Verify clinical data entered in case report forms is accurate and complete Resolve queries remotely and on site and guide site staff toward closure Use hardware and software for clinical study data review and [. .. ] items to resolution Manage site-level activities and communications to meet project objectives, deliverables and timelines Act as primary liaison with study site personnel or collaborate with the Central Monitoring Associate Train assigned sites and project-specific site team members Prepare for and attend Investigator Meetings and sponsor face-to-face meetings Participate in global clinical monitoring/ project staff meetings and clinical training sessions Support audit readiness, audit preparation and follow-up actions Requirements Bachelors degree or RN in a related [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Associate Director, Regulatory Affairs, Europe
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] with urgency and hold ourselves to a high standard of rigorall in service of patients. The Opportunity As part of our expanding European organization, we seek a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategic and handson Associate Director, Regulatory Affairs, Europe who will provide regulatory leadership for designated programs at Rev Med. The candidate will be responsible for the preparation end-to-end execution of regulatory MAA filings across the EU, EEA, UK and Switzerland for oncology programs, ensuring alignment of the European regulatory strategy with the [. .. ] between global and regional regulatory strategies. Act as a strategic partner to crossfunctional teams, including R D, Medical Affairs, Safety, Market Access, and Commercial. Ensure compliance with applicable European regulatory, pharmacovigilance, and governance requirements. Monitor and interpret evolving European regulatory requirements, guidelines, and trends, and communicate their impact across functions. Oversee external vendors and CROs to ensure timely, highquality regulatory submissions and approvals. Required Skills, Experience and Education Degree in biological or life sciences, pharmacy, medicine, or related fields. An advanced [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior Associate Global Safety (Local Safety Switzerland)
• Lavamünd, Kärnten
[. .. ] collaborators who achieve togetherresearching, manufacturing and delivering ever-better products that read over 10 million patients worldwide. Its time for a career you can be proud of. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us. SENIOR ASSOCIATE GLOBAL SAFETY (LOCAL SAFETY SWITZERLAND) LIVE What you will do In this vital role as a Senior Associate Global Safety (Local Safety Switzerland) you will support local pharmacovigilance activities in Switzerland and support provision of safety expertise to the local business. You will conduct core safety activities including data collection, processing, distribution and regulatory submission, based on appropriate training and assigned roles within the safety database and related systems. You will maintain compliance with Swiss legislation, Amgen policies [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
CRA II-multi-sponsor (north-east Germany)
• München, Bayern
CRA Germany multisponsor (northeast Germany) We are looking for an experienced Clinical Research
Associate (CRA) to join our team in Germany. The CRA will perform site qualification, initiation, monitoring, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] management, and closeout activities, ensuring compliance with regulatory, ICHGCP, and company SOPs. Job Responsibilities Perform site qualification, site initiation, interim monitoring, site management activities and closeout visits (performed onsite or remotely) ensuring regulatory, ICHGCP, and/[. .. ] protecting the confidentiality of each subject/ patient. Assess factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Assess site processes and conduct Source Document Review of appropriate site source documents and medical records. Verify required clinical data entered in the case report form (CRF) is accurate and complete. Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary, driving query [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Associate Director, Deputy QPPV, Europe
Führungs-/ Leitungspositionen
[. .. ] pathway. The Opportunity We are seeking a highly qualified and experienced EU-d QPPV to join our dynamic team and will report to the QPPV. The Deputy EU [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Qualified Person for Pharmacovigilance (Deputy EU QPPV) serves as the designated deputy to the EU QPPV and supports the oversight, maintenance, and continuous improvement of the companys European pharmacovigilance (PV) system. The role ensures compliance with European Union pharmacovigilance legislation, Good Pharmacovigilance Practices (GVP) , and applicable local requirements. The Associate Director, Deputy QPPV supports the QPPV in maintaining, executing, and continuously improving a fully compliant global Pharmacovigilance system. In the absence of the QPPV, this individual assumes full legal and functional responsibility for the safety of all marketed products and products under clinical development. Key Responsibilities Pharmacovigilance System Oversight PSMF [. .. ]
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 16 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:
- Jobgether (1 Job)
- Planet Pharma (1 Job)
- Revolution Medicines (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Associate Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Associate Jobs werden derzeit in Bayern (1 Jobs), Sachsen (1 Jobs) und Berlin (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Associate Jobs?
Pharmacovigilance Associate Jobs gehören zum Berufsfeld Pharmazie.
