33 Jobs für Pharmacovigilance Director
Stellenangebote Pharmacovigilance Director Jobs
Job vor 10 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
Senior
Director (m/f/x) DSE
Pharmacovigilance Operations (PVOps) Job Title: Senior Director (m/f/x) DSE Pharmacovigilance Operations (PVOps) Posting Start Date: 04/ 12/ 2025 Job Description For our Daiichi Sankyo European Headquarters [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (in Munich) , we are looking for a Senior Director (m/f/x) DSE Pharmacovigilance Operations (PVOps) . The Position Leads the PV [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. [. .. ]
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 am 11.07.2025 bei Jobleads gefunden
Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, German. . .
• 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 (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 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 gestern bei Jobleads gefunden
• 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 vor 12 Tagen bei Jobleads gefunden
Medical Director Clinical Development (Infectious Diseases)
• 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 full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 12 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] efforts on accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science, technology, and talent to get ahead of disease [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] together. The Medical Director Oncology Clinical Development, Breast and Gynecologic Cancerswill report to the Executive Medical Director, Clinical Development Lead (CDL) , Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSKs clinical portfolio and will also have responsibility for engaging in medical dialogues [. .. ] trial data, both directly as needed and/or via oversight of delegated medical review. Oversee blinded review of data packages intended for 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 publications (abstracts, posters, manuscripts) [. .. ]
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
Führungs-/ Leitungspositionen
Associate
Director, Distribution Quality Join to apply for the Associate Director, Distribution Quality role at Be One Medicines Be One continues to grow at a rapid pace with challenging [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most [. .. ] comply with GDP/ GSP requirements, maintaining the quality, safety and efficacy of pharmaceutical products throughout the supply chain. Cultivate productive and collaborative relationships across functional areas and geographies, including Commercial, Pharmacovigilance, Medical, Supply Chain, Operations, Internal and External Supply Quality, Regulatory Affairs and Regional Quality teams. Supervisory Responsibilities None Computer Skills PC literate with MS Office skills (Project Plan, Power Point, Outlook, Word, Excel, Visio) Veeva Vault, SAP UL Compliance Wire, UL Learn Share Ability to work on a computer (remotely) [. .. ]
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 04.12.2025 bei Jobleads gefunden
Global Head of Pharmacovigilance
Führungs-/ Leitungspositionen
[. .. ] Talent, part of The IN Group Bio Talent are delighted to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Global Head of Pharmacovigilance. This is a strategic leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. The role will direct safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. It is central to [. .. ] oversee budgets, resources, and department objectives in a dynamic environment. Fluency in English. If interested, please apply using the link or reach out to Ella Jobson on +498954194957. Seniority level Director Employment type Fulltime Job function Pharmaceutical Manufacturing and Biotechnology Research Referrals increase your chances of interviewing at Bio Talent by 2x. Get notified about new Head of Clinical Research jobs in Germany. #J-18808-Ljbffr 71599924 [. .. ]
Job am 03.12.2025 bei Jobleads gefunden
• 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
Associate Director Global Signal Management (m/f/d)
• 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
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 19.11.2025 bei Jobleads gefunden
Associate Director, deputy QPPV
• Heidelberg, Baden- Württemberg
Führungs-/ Leitungspositionen
About the Role Are you passionate about quality processes and patient safety? Do you have experience within
Pharmacovigilance and the QPPV role/ QPPV office related activities? If so, now [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is your chance to join Ascendis Pharma as our new Associate Director, deputy QPPV. Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in patients lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative Trans Con technology platform to fulfill our mission of developing new therapies that demonstrate best-in-class [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
• 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 11.07.2025 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 Physician [. .. ] 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 09.07.2025 bei Jobleads gefunden
Senior Director, PV Quality Management Lead (m/f/x) Europe
• München, Bayern
Führungs-/ Leitungspositionen
Work-Life-Balance
Senior
Director, PV Quality Management Lead (m/f/x) Europe Join to apply for the Senior Director, PV Quality Management Lead (m/f/x) Europe role at Daiichi Sankyo Europe Gmb H Senior [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director, PV Quality Management Lead (m/f/x) Europe Join to apply for the Senior Director, PV Quality Management Lead [. .. ] Skills And Professional Experience A minimum of Bachelors degree preferably in healthcare or life sciences required; Medical Doctor, Masters Degree, Pharmacist. Sufficient expertise in local, European and international regulatory and pharmacovigilance requirements. Work experience in pharmacovigilance of at least 12 years, experience, including both investigational and marketed products, and comprising at least 7 years management experience. Reads, writes and speaks English fluently. Develops quality expectations and supervises others within the function; actively develops and implements changes to improve quality within the [. .. ]
Job vor 13 Tagen bei Neuvoo.com gefunden
Tepsivo
Local Contact Person for Pharmacovigilance-LCPPV in Germany (Freelance)
• Berlin
Freiberuflich
Tepsivo is a young company on an ambitious mission to reshape the world of Pharma and
pharmacovigilance into a modern-day industry. Since our conception in 2020, weve become the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] worlds first fully digital global drug safety provider, with a genuine end-to-end PV system run by our in-house developed tools. Were looking for an experienced Local Contact Person for Pharmacovigilance (LCPPV) who is ready [. .. ] expect you to be able to operate in a highly regulated environment requiring full documentation of all performed activities. As the LCPPV in Germany, you will report directly to the Director of PV Services. General areas of responsibilities: Acting as LCPPV for Tepsivo Customers Support Tepsivo Customers in their local PV needs within Germany Reporting of local ICSRs via Tepsivo Platform Regulatory Intelligence within Germany Support in local audits and inspections Completion of CAPAs Liaising with the local regulatory authorities Our [. .. ]
Job vor 13 Tagen bei Neuvoo.com gefunden
Tepsivo
Local Contact Person for Pharmacovigilance-LCPPV in Germany (Freelance)
• Leipzig
Freiberuflich
Tepsivo is a young company on an ambitious mission to reshape the world of Pharma and
pharmacovigilance into a modern-day industry. Since our conception in 2020, weve become the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] worlds first fully digital global drug safety provider, with a genuine end-to-end PV system run by our in-house developed tools. Were looking for an experienced Local Contact Person for Pharmacovigilance (LCPPV) who is ready [. .. ] expect you to be able to operate in a highly regulated environment requiring full documentation of all performed activities. As the LCPPV in Germany, you will report directly to the Director of PV Services. General areas of responsibilities: Acting as LCPPV for Tepsivo Customers Support Tepsivo Customers in their local PV needs within Germany Reporting of local ICSRs via Tepsivo Platform Regulatory Intelligence within Germany Support in local audits and inspections Completion of CAPAs Liaising with the local regulatory authorities Our [. .. ]
Job vor 13 Tagen bei Neuvoo.com gefunden
Tepsivo
Local Contact Person for Pharmacovigilance-LCPPV in Germany (Freelance)
• Hamburg
Freiberuflich
Tepsivo is a young company on an ambitious mission to reshape the world of Pharma and
pharmacovigilance into a modern-day industry. Since our conception in 2020, weve become the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] worlds first fully digital global drug safety provider, with a genuine end-to-end PV system run by our in-house developed tools. Were looking for an experienced Local Contact Person for Pharmacovigilance (LCPPV) who is ready [. .. ] expect you to be able to operate in a highly regulated environment requiring full documentation of all performed activities. As the LCPPV in Germany, you will report directly to the Director of PV Services. General areas of responsibilities: Acting as LCPPV for Tepsivo Customers Support Tepsivo Customers in their local PV needs within Germany Reporting of local ICSRs via Tepsivo Platform Regulatory Intelligence within Germany Support in local audits and inspections Completion of CAPAs Liaising with the local regulatory authorities Our [. .. ]
1 von 2Weiter » Weitere Suchergebnisse laden »
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 33 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 (7 Jobs), Sachsen (5 Jobs) und Baden-Württemberg (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Director Jobs?
Pharmacovigilance Director Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
