23 Jobs für Pharmacovigilance Director
Stellenangebote Pharmacovigilance Director Jobs
Job vor 5 Tagen bei Jooble gefunden
Alira Health
• München
Führungs-/ Leitungspositionen
[. .. ] encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Biontech
Medical Director Clinical Development (Infectious Diseases)
• Mainz
Führungs-/ Leitungspositionen
Are you passionate about advancing medicine to unlock the full potential of the immune system against infectious diseases? Join Bio NTech as a Medical
Director in Clinical Development and play [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a key role in defining and executing the global development strategy for cutting-edge programs. Reporting to the VP of Clinical Development for Infectious Diseases, you will lead a cross-functional team to drive innovation in the design and execution of clinical trials that impact [. .. ] environment. Your contribution In this role, you will: Define the strategy and oversee the global execution of assigned Infectious Diseases programs, ensuring timely delivery Steer cross-functional teams, including Regulatory, Pharmacovigilance, and Biostatistics, providing clinical guidance for innovative solutions Guide the development and operationalization of Target Product Profiles, shaping clinical and submission plans Take ownership of clinical trials, leading protocol development, medical monitoring, and analysis for groundbreaking therapies Innovate trial design and accelerate program development to improve patient outcomes using advanced [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Takeda Pharmaceuticals International AG
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
A global biopharmaceutical company is seeking an experienced professional to ensure compliance and quality in clinical research and
pharmacovigilance. You will manage stakeholder relationships and direct audit strategies across business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] units to support effective transitions of R D activities. Ideal candidates have a BSc, relevant experience in the pharmaceutical industry, and excellent communication skills. The role also requires strategic thinking and a commitment to quality in regulated activities. J-[. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Takeda Pharmaceuticals International AG
Associate Director, Clinical PV Medical Quality, CPMQ Global Regions
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. OBJECTIVES: Provides oversight from a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates. Contributes to and implements the engagement strategy among R D, Business Units and affiliates and Quality to ensure a global framework and robust quality systems are in place for the transition of R D pipeline to the [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Overview Senior/ Medical
Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the [. .. ] 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with shifting priorities and deadlines. Communication Skills: Excellent verbal and written communication, able to convey complex ideas clearly to diverse audiences. Professional Credibility: Trusted medical professional with a strong foundation in both clinical and research settings. What We Offer [. .. ]
Job am 04.01.2026 bei Jobleads gefunden
Associate Director, Head of MSL Oncology, Germany
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Country Medical Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, [. .. ] national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, highquality medical information to both internal stakeholders and external customers. Strategic Cross Functional Collaboration and Insight Integration Ensure delivery of the German Oncology Medical Affairs field strategy and plan in close collaboration with business partners and aligned to the EU/ [. .. ]
Job am 01.12.2025 bei Jobleads gefunden
• 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 the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 and serve as the primary medical [. .. ] 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 5 Tagen bei Jobleads gefunden
Global Director, Clinical PV Medical Quality
• Schweiz, Kärnten
Führungs-/ Leitungspositionen
A global biopharmaceutical company is seeking an experienced professional to ensure compliance and quality in clinical research and
pharmacovigilance. You will manage stakeholder relationships and direct audit strategies across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] business units to support effective transitions of R D activities. Ideal candidates have a BSc, relevant experience in the pharmaceutical industry, and excellent communication skills. The role also requires strategic thinking and a commitment to quality in regulated activities. [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Schweiz, Kärnten
Führungs-/ Leitungspositionen
[. .. ] of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. OBJECTIVES: Provides oversight from a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates. Contributes to and implements the engagement strategy among R D, Business Units and affiliates and Quality to ensure a global framework and robust quality systems are in place for the transition of R D pipeline to the [. .. ]
Job am 26.12.2025 bei Jobleads gefunden
Medical Director-Oncology Clinical Development
• Zug
Führungs-/ Leitungspositionen
Medical
Director Oncology Clinical Development GSK Oncology Clinical Development is seeking a highly skilled and motivated Clinical Development Medical Director Oncology to join our dynamic Oncology Research and Development team. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The role requires a physician capable of developing and executing oncology clinical trials, supporting the successful clinical development, regulatory filing and initial [. .. ] directly as needed and/or via oversight of delegated medical review. Oversee review of data packages intended for internal and/or external IDMCs. Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies. Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries. Collaborate with Principal Investigators in the evaluation and assessment of data during dose escalation [. .. ]
Job am 15.12.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Jobticket
Medical
Director Clinical Development (Infectious Diseases) Join to apply for the Medical Director Clinical Development (Infectious Diseases) role at Bio NTech SE. Mainz, Germany; London, United Kingdom; Munich, Germany [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] full time Job ID: 10513 About the Role Are you passionate about advancing medicine to unlock the full potential of the immune system against [. .. ] thriving in a dynamic and fastpaced environment. Your contribution Define the strategy and oversee the global execution of assigned Infectious Diseases programs, ensuring timely delivery Steer crossfunctional teams, including Regulatory, Pharmacovigilance, and Biostatistics, providing clinical guidance for innovative solutions Guide the development and operationalisation of Target Product Profiles, shaping clinical and submission plans Take ownership of clinical trials, leading protocol development, medical monitoring, and analysis for groundbreaking therapies Innovate trial design and accelerate program development to improve patient outcomes using advanced [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
Senior Director (m/f/d) DSE Pharmacovigilance Operations (PVOps)
• München, Bayern
Führungs-/ Leitungspositionen
Senior
Director (m/f/d) DSE
Pharmacovigilance Operations (PVOps) Job Description: Job Title: Senior Director (m/f/d) DSE Pharmacovigilance Operations (PVOps) , Posting Start Date: 04/ 12/ 2025. For our Daiichi [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Sankyo European Headquarters (in Munich) , we are looking for a Senior Director to lead the PV Operations team at DSE which is responsible for [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
• Berlin
Führungs-/ Leitungspositionen
Director, Business Development-PV Projects For the past 20 years, Pro Pharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new 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 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. Essential Functions Develop and maintain long-term client relationships resulting in the expansion of our client base, [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Senior Director (m/f/x) DSE Pharmacovigilance Operations (PVOps)
• München, Bayern
Führungs-/ Leitungspositionen
Senior
Director (m/f/x) DSE
Pharmacovigilance Operations (PVOps) Job Alerts Link Job Title: Senior Director (m/f/x) DSE Pharmacovigilance Operations (PVOps) Posting Start Date: 04/ 12/ 2025 Job Description: Senior [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director (m/f/x) DSE Pharmacovigilance Operations (PVOps) The Position: Leads the PV Operations team at DSE which is responsible for the oversight and management [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] discovery organization, regulatory and others. Provides medical and scientific expertise for internal cross-functional team members for development of specific, hematology-oncology agents including discovery scientists, clinical scientists, biostatisticians, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. [. .. ] Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. Seniority level Director Employment type Full-time Job function Research Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 71927131 [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Director, Business Development-Compliance Quality Assurance
• Berlin
Führungs-/ Leitungspositionen
Director, Business Development-Compliance Quality Assurance Join to apply for the Director, Business Development-Compliance Quality Assurance role at Pro Pharma For the past 20 years, Pro Pharma has improved the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all [. .. ] 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 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. Essential Functions Develop and maintain long-term client relationships resulting in the expansion of our client base, [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
Director, Business Development-PV Projects
Führungs-/ Leitungspositionen
Director, Business Development-PV Projects page is loaded # # Director, Business Development-PV Projectslocations: Germany: Sweden: United Kingdom: Netherlandstime type: Full timeposted on: Posted Yesterdayjob requisition id: JR 8671For the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] past 20 years, Pro Pharma has improved the health and wellness of patients by providing advice and expertise that empowers [. .. ] 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 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. Essential Functions: Develop and maintain long-term client relationships resulting in the expansion of our client base, [. .. ]
Job am 03.12.2025 bei Jobleads gefunden
Early Clinical Development Medical Director, Oncology
• Zug
Führungs-/ Leitungspositionen
GSK Oncology Early Clinical Development is seeking a highly skilled and motivated Early Clinical Development Medical
Director-Oncology, to join our dynamic Oncology Research and Development team. In this role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the successful candidate will create a strong link between Clinical Development and Pre-clinical/ Discovery teams to improve forward and reverse translation and, thereby, increase the success of our Oncology clinical portfolio in the prostate cancer space. [. .. ] directly as needed and/or via oversight of delegated medical review. Oversee review of data packages intended for internal and/or external IDMCs. Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies. Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries. Collaborate with Principal Investigators in the evaluation and assessment of data during dose escalation [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
• Holzkirchen, Bayern
Führungs-/ Leitungspositionen
Associate
Director Global Signal Management (m/f/d) 6 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Job Description Sandoz continues [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic [. .. ] mentoring activities for new members Lead audits and inspections as an SME for Safety Signal Management Essential Requirements What youll bring to the role: At least 6 years experience in pharmacovigilance operations, including some handson experience in performing signal detection and management Additional handson experience in the preparation of aggregate reports, case processing, and risk management plans is a plus Excellent understanding of ICH GCP, GVP guidelines, local pharmacovigilance regulations and medical terminology Excellent understanding of signal detection process; understanding of [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
Senior Director, Global Process Owner-Quality Risk Management
Führungs-/ Leitungspositionen
Responsibilities The Senior
Director, Global Process Owner for Quality Risk Management, as a leader within the Global Quality Systems team, will establish and maintain the global quality system for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Quality Risk Management. They will provide strategic oversight and expertise for the global QRM process, including Global Quality System standards, practices, business processes, implementation tools [. .. ] with common QRM tools, how and when to apply them, and maintenance of a risk log or risk register. Prior experience working in at least two of Clinical Operations/ Development, Pharmacovigilance, Product Research Development or Commercial Manufacturing preferred. Role may be based at selected Lilly Locations in Europe or the US. At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Executive Medical Director Clinical Development Endocrinology, Europe
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] deserve brave science. For more information, visit neurocrine. com, and follow the company on Linked In, X and Facebook. (in collaboration with Abb Vie) About the Role: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Executive Medical Director, Europe is responsible for providing medical oversight of clinical programs in the endocrinology therapeutic area, including marketed products and investigational medications. The Executive Medical Director will help lead the strategy, planning, and execution of the clinical development plan, including Phase 1 to 4 clinical studies in collaboration with cross-functional project team members, including clinical operations, clinical pharmacology, biometrics, regulatory, drug safety/ pharmacovigilance. The Executive Medical Director will also partner with medical affairs, HEOR, and commercial to provide guidance on publication strategy, data generation needs, and label expansion opportunities for marketed products. Your Contributions (include, but are not limited to) : Oversight of the clinical development strategy in the endocrinology therapeutic area Oversight [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
Executive Director, Regulatory Affairs (Contract) Clinical European/ Global Focus
• Zug
Führungs-/ Leitungspositionen
Executive
Director, Regulatory Affairs (Contract) Clinical European/ Global Focus Join our Mission to Protect Humankind Vaxcyte is a clinicalstage vaccine innovation company engineering highfidelity vaccines to protect humankind from [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such [. .. ] clinical outcomes. Lead interactions and negotiations with global regulatory authorities for reconciliation of specific clinical and preclinical issues to expedite regulatory application submissions and approvals. Support regulatory requirements for safety/ pharmacovigilance notifications to regulatory authorities. Provide guidance on contemporary regulatory intelligence, statutory legislation and changes in regulatory authority requirements and expectations. Manage crossfunctional teams to demonstrate and ensure regulatory compliance. Optionally, people development and management may be expected. Requirements BA or BS in a relevant scientific or technical discipline, i. e. [. .. ]
Job am 01.11.2025 bei Jobleads gefunden
Director, Business Development-CE
• Berlin
Führungs-/ Leitungspositionen
Candidates must be located in Central Europe Company Overview: Rx Logix is a global leader in
pharmacovigilance solutions, providing innovative software and expert consulting services. Our team collaborates with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the advancement of medical and scientific research, Rx Logix values bold, innovative thinkers. We leverage the [. .. ] PV Surveillance Suite Platform to replace its legacy FAERS signaling system, utilizing our modules for advanced data analytics, signal detection, evaluation, signal management, and benefit-risk assessment. General Purpose: The Director, Business Development will report directly to the Vice President of Business Development for US and Europe of Rx Logix. Managing territory by selling directly into pharmaceutical companies and Contract Research Organizations (CROs) . Build and work the entire sales pipeline from prospecting for new business, to cold-calling, to getting [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Director pro Jahr?
Als Pharmacovigilance Director verdient man zwischen EUR 80.000,- bis EUR 120.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Director Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 23 offene Stellenanzeigen für Pharmacovigilance Director Jobs.
In welchen Bundesländern werden die meisten Pharmacovigilance Director Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Director Jobs werden derzeit in Bayern (5 Jobs), Berlin (3 Jobs) und Sachsen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Director Jobs?
Pharmacovigilance Director Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
