13 Jobs für Pharmacovigilance Scientist
Stellenangebote Pharmacovigilance Scientist Jobs
Job vor 6 Tagen bei Jobleads gefunden
[. .. ] delegated QPPV activities and maintain inspection readiness Serve as representative and point of contact for Health Authority Inspections and Internal Process Audits Requirements Doctorate degree and 2 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] years of industry pharmacovigilance experience, OR Masters degree and 4 years of industry pharmacovigilance experience, OR Bachelors degree and 6 years of industry pharmacovigilance experience, OR Associates degree and 10 years of industry pharmacovigilance experience, OR high school diploma/ GED and 12 years of industry pharmacovigilance experience Experience in signal detection, evaluation and management [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
GSK
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] are consistently applied across studies within a programme. Operating within the clinical strategy defined by the Clinical Development Lead (CDL) , the Senior Medical Director partners closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Senior Scientist and crossfunctional teams to guide the integration of physician expertise into study execution and programmelevel decisionmaking. The role serves as a senior member of the Clinical Matrix Team (CMT) , contributing to complex clinical decisions, regulatory interactions, and external scientific engagement. The Senior Medical Director provides oversight and guidance to [. .. ] supporting consistency and development of clinical capability Detailed Responsibilities: Medical Monitoring and Safety Oversight consistency in approach, patient safety, and protocol adherence Guide interpretation of safety data in collaboration with pharmacovigilance, supporting signal detection, escalation, and benefitrisk evaluation across the programme Participate in and contribute to safety review forums (e. g. , SRT, IDMC) , providing senior physician perspective on complex safety questions Ensure medical monitoring approaches are aligned across studies and consistent with regulatory and organisational standards Study Design and [. .. ]
Job am 26.07.2026 bei Mindmatch.ai gefunden
Bio Talent
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
Senior Director,
Pharmacovigilance, Remote + Switzerland/Germany office locations. Lead the future of pharmacovigilance in a strategic portfolio leadership role. Bio Talent is collaborating with an internationally growing pharmaceutical company. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are looking to appoint a Portfolio Owner in Pharmacovigilanceto take end-to-end accountability for the safety strategy of a global product [. .. ] pharmacovigilance experience within the pharma or biotech industry Strong expertise in post-marketing safety, benefit-risk management and PV strategy Experience in leadership roles such as Global Safety Lead, Safety Scientist, Therapeutic Area Lead, or similar Proven ability to lead teams and influence stakeholders in complex global environments Location: Switzerland or Germany This is an excellent opportunity for senior PV professionals looking to move beyond operational oversight and into a role with true strategic ownership and organisational impact. J-18808-Ljbffr [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Director, Pharmacovigilance
• Schweiz, Kärnten
Führungs-/ Leitungspositionen
Senior Director,
Pharmacovigilance, Remote + Switzerland/Germany office locations. Lead the future of pharmacovigilance in a strategic portfolio leadership role. Bio Talent is collaborating with an internationally growing pharmaceutical company. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are looking to appoint a Portfolio Owner in Pharmacovigilanceto take end-to-end accountability for the safety strategy of a global product [. .. ] pharmacovigilance experience within the pharma or biotech industry Strong expertise in post-marketing safety, benefit-risk management and PV strategy Experience in leadership roles such as Global Safety Lead, Safety Scientist, Therapeutic Area Lead, or similar Proven ability to lead teams and influence stakeholders in complex global environments Location: Switzerland or Germany This is an excellent opportunity for senior PV professionals looking to move beyond operational oversight and into a role with true strategic ownership and organisational impact. #J-18808-[. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
• Melsungen, Hessen
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten Betriebliche Altersvorsorge
Innerhalb des Qualitätsmanagements der Sparte Hospital Care suchen wir in der Abteilung Global
Pharmacovigilance and Patient Safety (GPVS) der B. Braun Melsungen AG zum nächstmöglichen Zeitpunkt einen Safety
Scientist (w/m/d) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] für das QPPV-Office/ die Veterinär-Pharmakovigilanz am Standort Melsungen. Das QPPV-Office bildet eine zentrale Governance-Funktion innerhalb des globalen Pharmakovigilanz-Systems für Humanarzneimittel der B. Braun Melsungen AG. Gemeinsam mit der QPPV stellt das Team die regulatorisch konforme Steuerung, kontinuierliche Weiterentwicklung und wirksame Überwachung des [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Safety Scientist (w/m/d) - QPPV-Office/ Veterinär-Pharmakovigilanz
• Melsungen, Hessen
Beratungs-/ Consultingtätigkeiten Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] Sharing Expertise. Unternehmen: B. Braun Melsungen AG Stellenstandort: Melsungen, Hessen, Deutschland Funktionsbereich: Qualität Arbeitsmodell: Hybrid Anforderungsnummer: 13849 Innerhalb des Qualitätsmanagements der Sparte Hospital Care suchen wir in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der Abteilung Global Pharmacovigilance and Patient Safety (GPVS) der B. Braun Melsungen AG zum nächstmöglichen Zeitpunkt einen Safety Scientist (w/m/d) für das QPPV-Office/ die Veterinär-Pharmakovigilanz am Standort Melsungen. Das QPPV-Office bildet eine zentrale Governance-Funktion innerhalb des globalen Pharmakovigilanz-Systems für Humanarzneimittel der B. Braun Melsungen AG. Gemeinsam mit der QPPV stellt das Team die regulatorisch konforme Steuerung, kontinuierliche Weiterentwicklung und wirksame Überwachung des [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] of Alexion with relevant customer groups Timely and complete reporting and presentation of account plans including KPIs to senior positions and accurate maintenance of the CRM database [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Collect and report pharmacovigilance information according to internal SOPs Represent their territories in regular territory reviews and account plan discussions Represent the respective country at national and international events and congresses Obey data protection law according Alexions policy and follow Alexions SOPs and compliance policies. You Will Need To Have B. A. or B. S. degree in a scientific or related field. Or qualified nurse or other degree-level ancillary medical staff (e. g. Physiotherapy or Clinical Research Scientist) and/or equivalent experience. 6+ years of sales experience preferably in niche/ orphan drug area Track record of achievement managing sales territory in a highly specialized area of medicine Must have established industry network and relationships within territory Excellent communication skills both verbal and written Influential presentation style with demonstrated [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Baar, Zug
Führungs-/ Leitungspositionen
[. .. ] safety and clinical integrity are maintained throughout study execution. Operating within the clinical strategy defined by the Clinical Development Lead (CDL) , the Medical Director partners closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Senior Scientist and crossfunctional teams to ensure that the physician perspective is fully integrated into study delivery. The role serves as a core member of the Clinical Matrix Team (CMT) , contributing to studylevel decisions, investigator engagement, and regulatory interactions. For more complex or multistudy programmes, the Medical Director may provide medical [. .. ] and safety oversight Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical review activities Interpret and contextualise safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefitrisk assessment at the study level Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews, and internal governance as required Ensure medical monitoring activities are conducted in compliance with GCP, ICH guidelines, and applicable regulatory [. .. ]
Job am 21.08.2026 bei Jobleads gefunden
• Berlin
[. .. ] therapies. 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. Job responsibilities Authoring and Quality review of Aggregate reports (PSURs/ PBRERs, PADERs/ Annual Reports/ ACO/ DSUR) for [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
• Hannover, Niedersachsen
Overview and key accountabilities The Medical
Scientist is a field-based medicalscientific expert in the assigned Therapeutic Area. The MS assumes full responsibility for all Medical activities within the assigned [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] territory and executes the field medical strategy under the guidance of the MS Lead. This involves gathering insights, medical education and communication, supporting clinical research projects, and [. .. ] which includes collaboration with investigators and study sites. Actively collaborating with the office and fieldbased national and international Medical Affairs team. Working collaboratively with personnel in Sales, Marketing, Clinical Research, Pharmacovigilance, Medical Communications, and other functions. Utilizing scientific resources to deliver impactful presentations in a variety of different settings. Contributing to the development of educational programs and materials. Traveling to appointments, meetings, and conferences on a frequent and regular basis, occasionally with short notice; including national and international travel. Essential background [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Medical Director, Oncology Clinical Development-Hematology
• Baar, Zug
Führungs-/ Leitungspositionen
[. .. ] safety and clinical integrity are maintained throughout study execution. Operating within the clinical strategy defined by the Clinical Development Lead (CDL) , the Medical Director partners closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Senior Scientist and cross-functional teams to ensure that the physician perspective is fully integrated into study delivery. The role serves as a core member of the Clinical Matrix Team (CMT) , contributing to study-level decisions, investigator engagement, and regulatory interactions. For more complex or multi-study programs, the Medical Director [. .. ] and safety oversight Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical review activities Interpret and contextualize safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefitrisk assessment at the study level Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews, and internal governance as required Ensure medical monitoring activities are conducted in compliance with GCP, ICH guidelines, and applicable regulatory [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] patients worldwide. We are a company in motion, growing, evolving, and investing in early development as a core engine of innovation. At Incyte, every idea begins with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] science and every scientist plays a part in shaping what comes next. The Role This position is responsible for implementing early clinical development efforts for Incytes Dermatology, Immunology, Rheumatology products (preclinical candidate nomination through transition to registrational studies) . Duties and Responsibilities Leads development efforts for assets post-candidate selection through first in human [. .. ] organization, regulatory and others. Provides medical and scientific expertise for internal cross-functional team members for development of specific, dermatology and immunology agents including discovery scientists, clinical scientists, biostatisticians, pharmacokinetics, pharmacovigilance, and clinical operations. Supports interactions with global regulatory bodies including the FDA, EMA, PMDA and TGA and ethics committees to accomplish tasks related to product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and other regulatory documents. [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Director Real World Evidence Scientist (Oncology) (all genders)
• Darmstadt, Hessen
Führungs-/ Leitungspositionen
[. .. ] world evidence is reshaping how medicines are developed, approved, and valued and in this role, you will be at the forefront of that transformation. As a Director [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Real-World Evidence Scientist in Oncology, you will own and drive the end-to-end RWE strategy for one or more complex, high-priority oncology programs, operating as a recognized scientific authority across the organization and beyond. You will define and lead the integration of RWE into clinical development and regulatory strategies, working directly [. .. ] collection. You are proficient in working with federated data networks and familiar with data standards such as OMOP CDM or FHIR, and bring strong methodological skills spanning epidemiology, pharmacology, and pharmacovigilance. You have a proven track record of leading RWE strategy at a global program level, navigating complex, matrixed organizations and collaborating effectively across clinical development, regulatory affairs, and market access functions. You bring experience in regulatory and/or payer submissions and interactions, and a thorough understanding of the evolving regulatory [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Scientist pro Jahr?
Als Pharmacovigilance Scientist verdient man zwischen EUR 70.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Scientist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 13 offene Stellenanzeigen für Pharmacovigilance Scientist Jobs.
In welchen Bundesländern werden die meisten Pharmacovigilance Scientist Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Scientist Jobs werden derzeit in Niedersachsen (6 Jobs), Hessen (3 Jobs) und Sachsen-Anhalt (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Scientist Jobs?
Pharmacovigilance Scientist Jobs gehören zum Berufsfeld Pharmazie.
