53 Jobs für Pharmacovigilance Manager
Stellenangebote Pharmacovigilance Manager Jobs
Job am 12.02.2026 bei Jobleads gefunden
• Berlin
[. .. ] introduce new therapies. Pro Pharma partners with its clients through an advisebuildoperate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research [...]
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[...] solutions, quality compliance, pharmacovigilance, medical information, and R D technology, Pro Pharma offers an endtoend suite of fully customizable consulting solutions that derisk and accelerate our partners most highprofile drug and device programs. Responsibilities The Senior PV Manager will be responsible for Signal Detection Services provided to clients. Commitment to Diversity, Equity Inclusion We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and [. .. ]
Job vor 5 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
Quality Assurance GVP Manager (m/w/d)
• Freiburg
Homeoffice möglich
[. .. ] well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks As the Quality Assurance [...]
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[...] (QA) GVP Manager within the GCP and GVP Quality Department, you will play a pivotal role in maintaining and enhancing the quality management framework in alignment with Good Pharmacovigilance Practice (GVP) guidelines. By collaborating with internal teams and external partners, you will ensure regulatory compliance and foster a robust culture of vigilance and safety. Your primary responsibilities will include, but are not limited to: Audits and Inspections: Plan, Conduct, and Follow Up on Pharmacovigilance Audits including oversight and training [. .. ]
Job am 04.02.2026 bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Homeoffice möglich
[. .. ] achieved by working together. That is why we are looking for: Your tasks Supporting the Head of Global Safety QPPV Office/ EU QPPV/ Graduated Plan Officer in [...]
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[...] the fulfillment of pharmacovigilance obligations, including: Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e. g. KPIs, PSMF) Collection, systematic documentation and evaluation of all necessary information in connection with indications [. .. ] at or call 0761 1514-253. We look forward to receiving your application via our online portal. . Dr. Falk Pharma Gmb H sucht in Freiburg eine/n Global Safety Project Manager-Operations Compliance (m/f/d) (ID-Nummer: 13602237) 79200198 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Rhythm Pharmaceuticals
Scientific Affairs Manager, Austria
• AT- 9 Wien
[. .. ] GSA team, you will focus on advancing medical and scientific initiatives in Rare MC4R pathway diseases. In close collaboration with the national and international Medical Affairs teams, [...]
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[...] the Scientific Affairs Manager (SAM) will provide scientific leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Austria. Responsibilities and Duties Serve as the Scientific Affairs Manager for Austria and as a member of the international Medical Affairs team. Contribute [. .. ] and assistance with patient recruitment. Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements. Collaborate closely with Commercial, Regulatory, Pharmacovigilance and Market Access. Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations. Participate in local medical and cross-functional projects and initiatives. Ensure effective and compliant communication with internal and external stakeholders. Support the commercial team and HCPs with knowledge building around the efficacy and safety of [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Grünenthal Group
• AT- 9 Wien
[. .. ] analyzing scientific insights from the field to inform medical and commercial strategies. Shaping the scientific content of congresses, symposia, advisory boards, webinars, and other medical education events. [...]
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[...] Supporting regulatory and pharmacovigilance teams with your therapeutic expertise. What Youll Bring To The Table To make the most of this role and grow successfully, you should bring: A successfully completed degree in Medicine, Pharmacy, or a natural science discipline, ideally complemented by a Ph D. At least 3 years of relevant experience in the [. .. ] structured, evidencebased approach to work. Proven ability to effectively manage external agencies and scientific content providers. Fluency in German and businesslevel English, both written and spoken. Jan Jastorff, the Hiring Manager J-18808-Ljbffr 82511742 [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
Senior Clinical Evaluation Manager (m/f/d)
• AT- 9 Wien
[. .. ] history of my Sugr Roche. Heres what were looking for: We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as [...]
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[...] a Senior Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experince with clincial evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] state-of-the-art. Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space. Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety. Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset. Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans. Excellent communication, presentation, and interpersonal skills. A true team player is a must. Fluency in English is required. [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
Colgate
• AT- 9 Wien
[. .. ] of life and programmes that enrich communities. A career at Colgate-Palmolive offers global experience, constant challenge, and development opportunities in a respectful work/ life environment. Job Title [...]
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[...] Scientific Affairs Manager (f/m/d) Travel Required? : Travel-25 of time Posting Start Date: 04/ 02/ 2026 Hybrid No Relocation Assistance Offered Job Number #171542-Vienna, Vienna, Austria Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising in Oral Care, Personal Care, Home [. .. ] MDR for any device-related items National implementation of EU cosmetics rules, plus local advertising and professional conduct codes Other skills: Scientific communication, Stakeholder mapping, Instructional tools, Data ethics and pharmacovigilance, Measurement and impact, Project management, Cultural agility, Digital savviness German (C1+) and very good level of English Field readiness (60 of travel) : Comfortable with frequent travel across Austria/ Switzerland; able to manage university and clinic calendars and congress circuits Inclusion and Equal Opportunity Our Commitment to Inclusion Our journey [. .. ]
Job vor 14 Tagen bei Mindmatch.ai gefunden
Roche
Senior Clinical Evaluation Manager (m/f/d)
• AT- 9 Wien
[. .. ] Roche here. Here s what we re looking for: We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as a [...]
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[...] Senior Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experience with clinical evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] state-of-the-art Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans Excellent communication, presentation, and interpersonal skills A true team player is a must Fluency in English is required. [. .. ]
Job am 09.02.2026 bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
• AT- 9 Wien
[. .. ] Roche here. Here s what we re looking for: We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as a [...]
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[...] Senior Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experience with clinical evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] for medical devices) ; solid understanding of Diabetes and CGM technologies; ability to manage relationships with Diabetes-focused experts. Clinical safety knowledge: Strong understanding of clinical trial design, data analysis, pharmacovigilance/ device safety; experience as Study Safety Officer is an asset. Communication teamwork: Excellent communication, presentation, and interpersonal skills; true team player; fluent in English; German proficiency is highly advantageous. In Austria, we disclose the minimum salary according to our collective agreement: gross EUR 3, 843 per month for this position. [. .. ]
Job am 08.02.2026 bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
Senior Medical Manager/ Senior Clinical Evaluation Manager
• AT- 9 Wien
[. .. ] # # # Heres what were looking for: We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as a Senior [...]
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[...] Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experince with clincial evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] state-of-the-art. Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space. Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety. Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset. Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans. Excellent communication, presentation, and interpersonal skills. A true team player is a must. Fluency in English is required. [. .. ]
Job am 14.12.2025 bei Jobleads gefunden
• München, Bayern
Abgeschlossenes Studium
30+ Urlaubstage
[. .. ] Erweiterung unseres Teams suchen wir mit Verantwortung für die Produkte der Strathmann Gmb H und Co. KG und mit Dienstsitz am Standort Grünwald bei München zum nächstmöglichen [...]
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[...] Termin in Vollzeit einen Manager Medical Affairs (m/w/d) . Im Bereich Medical Affairs Beantwortung externer Anfragen und Beratung von Ärzten, Apothekern und Patienten Erstellung und Freigabe medizinisch-wissenschaftlicher Informationen zu Produkten und Indikationen Schulung von Außendienstmitarbeitern, Ärzten und Apothekern Erstellung und Aktualisierung von Fach- und Gebrauchsinformationen, Schulungsmaterialien und Publikationen Aufbau Pflege von Netzwerken [. .. ] für medizinische Fachkreise und Patienten Interdisziplinäre Zusammenarbeit mit cross-funktionalen Teams zur ganzheitlichen und effektiven Umsetzung medizinischer Strategien Beurteilung neuer Produkte z. B. hinsichtlich Evidenz, Effektivität und Verträglichkeit Im Bereich Pharmacovigilance Stellvertretung der QPPV: Unterstützung bei Pflege des PV-Systems und bei Erstellung von Risikomanagementplänen; zeitliche Vertretungsregelungen Erfassung, Dokumentation, Meldung und Nachverfolgung unerwünschter Arzneimittelwirkungen Unterstützung der QPPV bei Bewertung von Verdachtsfällen hinsichtlich Kausalität, Bekanntheit oder verändertem Nutzen Risiko Verhältnis Erstellen von periodischen Sicherheitsberichten (PBRER, DSUR) und von CCDS Case Narratives zu [. .. ]
Job am 01.12.2025 bei Jobleads gefunden
Country Medical Director, Germany
• München, Bayern
Führungs-/ Leitungspositionen
Reporting to the General
Manager (GM) Germany, the Country Medical Director Germany is responsible for the development and execution of the German medical affairs strategy and programs that support [...]
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[...] the successful commercialization of current and future Jazz Pharmaceuticals products. As a strategic partner to the GM, the incumbent will lead the German Medical Affairs department [. .. ] accordance with Jazz values and codes of practice. Ensure full compliance with applicable German laws, including AMG and HWG, and Jazz Pharmaceuticals Code of Conduct. Maintain strict adherence to Jazz Pharmacovigilance Policy. Foster strong partnerships with KEEs by delivering balanced, evidencebased scientific information, ensuring decisionmakers are equipped to appropriately position Jazzs portfolio within treatment guidelines and protocols. Participate in relevant scientific congresses to remain current with medical advancements and to actively support national KEE engagement. Contribute to establishing Jazz EU/ INT [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Glattbrugg, Zürich Zuerich
[. .. ] impact for patients. We are building a future-ready team that thrives in dynamic biotech ecosystems. The Post Marketing, Medical Coding and Device Safety PV Scientists Lead is [...]
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[...] the line manager of PV Scientists who contribute to lifecycle safety and risk management activities for CSL products, particularly for products with existing open marketing authorizations. The role provides strategic input into processes and ensures scientific analyses are conducted with rigor to enable proactive safety management. Responsibilities Ensure implementation of GVP-compliant PV standards and processes by the Pharmacovigilance Scientists, Device expert, and Medical coding expert under their management. Collaborate cross-functionally with relevant individuals within PV and with key stakeholders; support PVS for products in post-marketing and those in ongoing clinical development as required. Partner with Signal Management, Governance, Literature and Aggregate Reports, and Risk Management Heads [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Regulatory Affairs Manager
• Frankfurt, Hesse
We are seeking an experienced Regulatory Affairs
Manager to support and maintain our portfolio of generic medicinal products and marketed brands in Germany and the EU. Based in Frankfurt, [...]
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[...] you will be responsible for lifecycle management activities, regulatory strategy implementation, and ensuring continued compliance with German (Bf Ar m/PEI) and European (EMA) regulatory requirements. This is a key role within the Regulatory Affairs team, collaborating cross-functionally with Quality, Supply Chain, Pharmacovigilance, Medical Affairs, and Commercial teams. Key Responsibilities Regulatory Strategy Submissions Develop and implement regulatory strategies for generic and established medicinal products in Germany and EU markets. Prepare, compile, and submit variations (Type IA/ IB/ II) , renewals, line extensions, and marketing authorisation applications (MAAs) where applicable. Manage national (DE) , [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Wien
Beratungs-/ Consultingtätigkeiten
[. .. ] Roche here. Here s what we re looking for: We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as a [...]
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[...] Senior Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experience with clinical evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] state-of-the-art Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans Excellent communication, presentation, and interpersonal skills A true team player is a must Fluency in English is required. [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
Senior 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 [...]
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[...] and Safety (eg. Pharmacovigilance) . As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R D) space managing teams and planning, organizing, and tracking all aspects of delivery. You will analyze interesting problems, build insightful solutions, and develop close working relationships with stakeholders [. .. ] IT Consulting, and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Veeva Systems by 2x Get notified about new Senior Business Consultant jobs in Berlin, Germany. DG Business Development Manager-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 80761906 [. .. ]
Job am 12.02.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] cardiology, pediatrics, emergency medicine are preferred) with following experience:-Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. [...]
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[...] -Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. -Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company. -Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in CRO/ Pharma company. Clinical Practice Experience Qualifications Clinical practice experience of minimum 4 years is mandatory. Typical candidates have 1015 years of working experience (clinical practice +/-industry) post residency/ fellowship. Its not necessary that they are licensed in US or a specific country (check local legal requirements) [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
Senior Medical Manager/ Senior Clinical Evaluation Manager
• Wien
[. .. ] Roche. # # # Heres what were looking for:We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as a Senior [...]
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[...] Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experince with clincial evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] state-of-the-art. Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space. Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety. Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset. Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans. Excellent communication, presentation, and interpersonal skills. A true team player is a must. Fluency in English is required. [. .. ]
Job am 06.02.2026 bei Jobleads gefunden
Global Safety Project Manager-Operations Compliance (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Global [...]
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[...] Safety Project Manager-Operations Compliance (m/f/d) Responsibilities Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e. g. KPIs, PSMF) Collection, systematic documentation and evaluation of all necessary information [. .. ] use, abuse or counterfeit drugs Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Passing on necessary information to pharmacovigilance departments at service providers, licensees/ licensors, distribution partners and affiliates within the framework of contractual pharmacovigilance agreements Support with periodic reconciliations with partners, subsidiaries and internal departments Support in the preparation of pharmacovigilance agreements Support in creation and maintenance of pharmacovigilance system master file (PSMF) Overview of the pharmacovigilance system [. .. ]
Job am 28.01.2026 bei Jobleads gefunden
Medical Affairs Manager (f/m/d)
• Garching bei München, Bayern
Homeoffice möglich
Jobticket
[. .. ] congresses Build and maintain strategic relationships with Key Medical Experts (KMEs) and facilitate advisory boards and scientific meetings Provide medical expertise across the full drug development lifecycle, [...]
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[...] including Safety and Pharmacovigilance support Ensure compliance with regulatory, ethical, and scientific standards (MLR review, GCP, promotional compliance) Manage external vendors and ensure rapid, compliant responses to emerging data and competitive intelligence Your profile Master Degree/ Ph D preferred with a strong scientific and medical background At least 3 years of industry experience with a [. .. ] pre-launch Medical Affairs activities in regional and global settings Scientific expertise in Oncology combined with solid knowledge of ICH-GCP and relevant regulatory and compliance guidelines Confident, hands-on manager with experience working cross-functionally (e. g. , Regulatory, Compliance, Corporate Communications) Proven expertise in digital medical communications, including platforms such as Veeva CRm/Promomats and SEO/ SEM fundamentals Excellent presentation and communication skills, with the ability to synthesize and present complex scientific data to expert audiences Fluent in business [. .. ]
Job am 27.01.2026 bei Jobleads gefunden
Global Pharmacovigilance QA Manager
[. .. ] in-house development pipeline; and a specialized drug discovery engine focused on small-molecule drugs that can change the treatment paradigm for many patients. We are looking for a [...]
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[...] Global Pharmacovigilance QA Manager to join our team Job Responsibilities The Global Pharmacovigilance QA is a strategic role that drives enhanced compliance throughout the PV domain to support the obligation of the Marketing Authorization Holders and appointed QPPV, to maintain and improve a Global PV system in accordance with international regulations. He/ She independently [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
Engagement Manager-R D (Remote)
• Berlin
[. .. ] our leading R D consulting practice is a strategic priority for Veeva, with high visibility within the company and to leaders of the wider Life Sciences industry. [...]
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[...] As an Engagement Manager, you will manage complex and novel consulting projects for Veeva customers in the research and development (R D) space managing teams and planning, organizing, and tracking all aspects of delivery. You will support building our brand in the market, developing our customer network, and identifying and acquiring new projects to 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 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 [. .. ]
Job am 02.01.2026 bei Jobleads gefunden
Medical Science Liaison Manager für Bayern/ Baden-Würtemberg
• Hannover, Niedersachsen
[. .. ] 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, [...]
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[...] 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 17.12.2025 bei Jobleads gefunden
Clinical Safety Manager-Pharmacovigilance/ Drug Safety
• München, Bayern
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety
Manager to join our team in Munich. This position plays a key role [...]
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[...] in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the companys success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Manage Clinical [. .. ]
Job am 16.12.2025 bei Jobleads gefunden
Clinical Trial Manager-single sponsor
• München, Bayern
[. .. ] Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates [...]
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[...] to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problemsolving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation point [. .. ] of other functions roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA) . Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central Monitors assigned to the study and routinely assesses studyspecific process and training compliance, CMP compliance, and identifies emerging risks. May develop and support execution of corrective action plans at site and study level. [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Manager pro Jahr?
Als Pharmacovigilance Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 53 offene Stellenanzeigen für Pharmacovigilance Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Manager Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Pharmacovigilance Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Manager Stellenangebote:
- Dr. Falk Pharma GmbH (8 Jobs)
- F. Hoffmann- La Roche AG (2 Jobs)
- Alexion Pharmaceuticals (2 Jobs)
- Pro Pharma Group (2 Jobs)
- Eraneos (2 Jobs)
- Rhythm Pharmaceuticals (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Manager Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Manager Jobs werden derzeit in Bayern (11 Jobs), Niedersachsen (8 Jobs) und Berlin (6 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Manager Jobs?
Pharmacovigilance Manager Jobs gehören zum Berufsfeld Pharmazie.
