28 Jobs für Pharmacovigilance Director
Stellenangebote Pharmacovigilance Director Jobs
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical
Director/ Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions The role includes [. .. ] Adverse Events (AEs) . # # May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. # # May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance department. # # May perform medical review of adverse event coding. # # Performs review of the Clinical Study Report (CSR) and patient narratives. [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Sr Medical Director
• Bayern
Führungs-/ Leitungspositionen
[. .. ] site engagement. Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews. Contribute to clinical study reports (CSRs) , regulatory submissions, and medical writing. Collaborate with [...]
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[...] Clinical Operations and Pharmacovigilance teams. Qualifications MD or Ph D with deep expertise in the therapeutic area. Extensive experience in clinical development. Strong strategic thinking and leadership capabilities. Equal Opportunity Employer GE Health Care is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical
Director/ Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] science involvement on assigned trials, serve as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development activities. Essential [. .. ] of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance department. May perform medical review of adverse event coding. Performs review of the Clinical Study Report (CSR) and patient narratives. Attends Kick-Off meetings, weekly team meetings, and client [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
Medical Director
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
The Medical
Director will support clinical trials across early to late development phases, contributing to clinical strategy, safety oversight, and data interpretation. This role involves collaboration across crossfunctional teams to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deliver on clinical development goals and regulatory milestones. This is a Hybrid position. Key Responsibilities Draft and review clinical trial documents (protocols, IBs, ICFs, CSRs) . Serve as medical monitor for clinical trials, including oversight of external CROs. Oversee safety data reporting in coordination with safety and pharmacovigilance teams. Support study data interpretation, efficacy/ safety analyses, and DSMB activities. Contribute to clinical and regulatory strategies and interactions with health authorities. Engage with investigators, KOLs, and advisory boards. Represent medical input across internal teams and external meetings. Qualifications Medical degree (MD) required. Minimum 5 years of clinical and/or [. .. ]
Job am 21.03.2026 bei Jobleads gefunden
• Gräfelfing, Bayern
Führungs-/ Leitungspositionen
Your mission We are looking for an experienced and strategic Medical
Director (m/f/x) to provide medical leadership for a mature global Phase 3 program in relapsing Multiple Sclerosis. In this [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role, you will combine deep strategic understanding of MS clinical outcomes with handson medical monitoring expertise to support the successful execution of a registrational study, evaluating safety and efficacy. Clinical [. .. ] 3 results to support global registration, reimbursement strategies, and scientific publications. Medical Trial Oversight: Provide handson medical monitoring for the ongoing Phase 3 trial, including review activities during data cleaning. Pharmacovigilance Support: Partner with the Pharmacovigilance team on medical assessment of safety cases, including review and preparation of narratives for serious adverse events (SAEs) . Leadership in Regulatory Interactions: Serve as a medical leader in planned interactions with regulatory authorities, ensuring alignment on clinical evidence and program strategy. Your profile Medical [. .. ]
Job am 01.03.2026 bei Jobleads gefunden
Medical Director Safety
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] core. A dynamic international environment empowering you to learn, develop and grow. Dont hesitate to connect with us during the recruitment process to learn more Position Summary [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As a Medical Director for Clinical Trial/ Research Safety you will provide expert safety leadership and input to clinical development programs for nutritional solutions and therapeutics across the lifespan, and ensure safety compliance with regulatory frameworks applicable to pharma, medical nutrition and food for medical purposes (FSMP) . A Day in the Life of [. .. ] trial designs Respond to inquiries regarding safety issues and collaborate closely with regulatory teams for health authority responses for nutritional solutions Support a core team working on end-to-end pharmacovigilance for nutrition therapeutics with signal evaluation and risk management This position will have functional/ dotted line alignment to internal patient safety risk management governance frameworks What Will Make You Successful Medical degree, Md/Ph D, preferably with specialization in one of the following areas: internal medicine/ gastroenterology/ pediatrics/ clinical pharmacology. Swiss [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
• Ulm, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] and flexible environment with a strong patient focus and enterprise mindset. Experienced and adept at working collaboratively across different cross-functional teams such as commercial, R D, health [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes, regulatory, pharmacovigilance and compliance and others. Strong record of leadership with the appropriate skills working in a matrix set-up. Able to translate complex scientific content into what this means in medical practice for the HCP and patient. JOB CONDITIONS: Position based in the UK or Germany (flexible location) . International travel [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical 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 vor 3 Tagen bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As Associate
Director Audit Management, you will play a pivotal role in ensuring the quality and compliance of Bio NTechs clinical trials and processes. As part of the Global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to regulatory standards and fostering continuous improvement in clinical development activities. Your Contribution: Lead global audits with a focus on clinical investigator sites and vendor audits in the EU, UK, [. .. ]
Job am 24.04.2026 bei Jooble gefunden
Gilead Sciences
Sr Director, Patient Safety-Deputy EU-QPPV
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Führungs-/ Leitungspositionen
[. .. ] an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Deputy EU QPPV (m/f/d) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Senior Director, Patient Safety Help shape how we protect patients across the EEA. In this highly visible leadership role, you will partner closely with the EU QPPV and the broader Patient Safety organization to ensure our pharmacovigilance system remains robust, inspection-ready, and responsive to emerging safety needsso patients can benefit from our medicines with confidence. Role at a glance As Deputy EU QPPV, you act as the designated back-up for the EU QPPV during periods of absence and provide day-to-day operational leadership within [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
The Associate
Director, Safety Sciences provides scientific expertise for medical safety tasks. Core responsibilities include safety data review and analysis from different sources, periodic report authoring and the oversight [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of the safety surveillance activities for the assigned program (s) . The Safety Scientist ensures that all processes are conducted according to Bio NTech s [. .. ] inspections for key safety processes such as Safety Surveillance and aggregate report generation A Good Match: Advanced degree in life sciences/ healthcare; Ph D in a relevant discipline or post-doctoral pharmacovigilance certification preferred At least 5 years of experience in clinical research with significant exposure to pharmacovigilance activities within biotech/ pharmaceutical industries or CROs Expert knowledge of pharmacovigilance laws/ regulations as well as GCP/ GVP guidelines Proven experience in designing and implementing clinical safety processes/ tools and assessing/ reporting safety data [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Medical Director Clinical Development (Infectious Diseases)
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] play 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 am 08.04.2026 bei Jooble gefunden
Incyte Corporation
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Führungs-/ Leitungspositionen
[. .. ] most strategic markets, the company is strengthening its Public Affairs team to shape the next phase of growth. As such, we are creating a pivotal role to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead this ambition: Director of Public Affairs Inflammation and Autoimmunity (IAI) This position will define how Incytes strategy for immune-mediated dermatological conditions is understood, trusted and embraced by the German healthcare ecosystem. It will ensure stakeholder alignment, policy enablement, and long-term market shaping to unlock innovation and access for patients. The Role [. .. ] access enablers and reputation metrics Provide external intelligence and ecosystem insight to senior leadership and cross-functional teams Partner closely with Medical, Market Access, Commercial, HEOR, Regulatory, Legal, Compliance and Pharmacovigilance Ensure excellence in governance, ethics and compliance across all external engagements You will combine strategic vision, operational excellence and executive presence. Your Profile You bring: 810+ years of experience in healthcare public affairs, patient advocacy and communications Very good understanding of healthcare environment in Germany Knowledge of the area of [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
Senior Director Medical Affairs-Neurology
• Region Donau- Iller, Württemberg; Regierungsbezirk Tübingen; Württemberg Ulm, DE
Führungs-/ Leitungspositionen
[. .. ] and flexible environment with a strong patient focus and enterprise mindset. Experienced and adept at working collaboratively across different cross-functional teams such as commercial, R D, health [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes, regulatory, pharmacovigilance and compliance and others. Strong record of leadership with the appropriate skills working in a matrix set-up. Able to translate complex scientific content into what this means in medical practice for the HCP and patient. JOB CONDITIONS: Position based in the UK or Germany (flexible location) . International travel [. .. ]
Job gestern bei Jobleads gefunden
• Basel, Basel- Stadt
[. .. ] Aufbau und Pflege eines starken Netzwerks mit internen wie externen Stakeholdern, einschließlich enger Zusammenarbeit mit europäischen und globalen Teams Gewährleistung der Compliance und Einhaltung aller relevanten Kodizes, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatorischen Anforderungen und Pharmacovigilance Vorgaben Fachliche und personelle Führung, Motivation und Weiterentwicklung des Product Management Teams sowie Förderung einer leistungsorientierten, lernenden Teamkultur Verantwortung für das Bereichsbudget inklusive Planung, Steuerung und Controlling Leitung strategisch bedeutender, funktionsübergreifender Projekte mit hoher Relevanz für die Schweizer Vertriebsgesellschaft Aktive Mitarbeit im Leadership Team und Mitgestaltung der langfristigen strategischen Ausrichtung [. .. ] in diverse Businessprozesse Fortschrittliche Anstellungsbedingungen (e. g. Lunchcard, Zuschlag zum öffentlichen Verkehr, Option für mobiles Arbeiten) Zentrale Lage nur wenige Gehminuten entfernt vom Bahnhof Basel SBB Funktion: Marketing Berichtet an: Director Marketing Kontakt: Maria Herzog, Human Resources Pre Employment Screening: Vor der Bestätigung eines Beschäftigungs-/ Beförderungsangebots führt die Mepha Schweiz AG eine angemessene Überprüfung Ihrer Angaben und eine Sicherheitsüberprüfung Ihrer Person durch, soweit dies gesetzlich zulässig ist. Wenn Sie diese Phase des Bewerbungsprozesses erreichen, erhalten Sie vor der Überprüfung und Sicherheitsüberprüfung [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Senior Medical Director, Oncology Clinical Development-GU
• Zug
Führungs-/ Leitungspositionen
Site Name: UK London New Oxford Street, Stevenage, Switzerland-Zug, USA-Massachusetts-Waltham, USA-Pennsylvania-Upper Providence, Warsaw Posted Date: May 1 2026 The Senior Medical
Director, Oncology Clinical Development GU will report to [...]
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[...] the Executive Medical Director, Clinical Development Lead, Oncology Clinical Development. The Sr. 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 with relevant internal [. .. ] for clinical trials including active participation in realtime medical monitoring of studies, including patient eligibility assessment, study design questions and medical data review. 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 vor 4 Tagen bei Jobleads gefunden
• Schwyz
Führungs-/ Leitungspositionen
[. .. ] other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity Reporting to the VP, Medical Affairs, Europe, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Senior Medical Director for Thoracic Oncology (Lung) provides strategic and operational medical leadership across the European region for the lung cancer portfolio. This role contributes to the development and execution of the regional medical strategy in alignment with global objectives, ensuring scientific excellence, patient centricity, and compliance. The position serves as a key [. .. ] and Grants teams to integrate patient perspectives and support independent medical education. Support scientific congress activities and ensure alignment of medical communications within compliance standards. Ensure adherence to all regulatory, pharmacovigilance, and medical governance requirements. Required Skills, Experience And Education Advanced degree (MD, Ph D, Pharm D) in a relevant medical/ scientific field. 1215 years of experience in biotech or pharmaceutical industry, with strong focus in Medical Affairs. Deep scientific expertise in thoracic oncology, particularly NSCLC and biomarkerdriven lung cancers (e. g. , [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Senior Medical Director, Oncology Clinical Development-GU
Führungs-/ Leitungspositionen
Site Locations: UK London New Oxford Street, Stevenage, Switzerland-Zug, USA-Massachusetts-Waltham, USA-Pennsylvania-Upper Providence, Warsaw. Posted Date: May 1 2026. The Senior Medical
Director, Oncology Clinical Development-GU will report to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Executive Medical Director, Clinical Development Lead (CDL) , Oncology Clinical Development. The Sr. 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 with [. .. ] for clinical trials including active participation in realtime medical monitoring of studies, including patient eligibility assessment, study design questions and medical data review. 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 vor 8 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Executive
Director, Regulatory Strategy page is loaded # # Executive Director, Regulatory Strategyremote type: Hybridlocations: CH Allschwiltime type: Full timeposted on: Posted Todayjob requisition id: R6763 # # Who [...]
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[...] We Are:At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We [. .. ] of programs in a therapeutic area (TA) , overseeing and directing all regulatory activities across the entire product lifecycle. Drives collaboration with cross-functional partners (eg, Clinical, Quality, Drug Safety Pharmacovigilance, Legal, Government Affairs Public Policy, Patient Advocacy) to ensure consideration of regulatory perspectives. Devotes significant time to talent and workforce development. Sets the tone for the group from a leadership perspective. Performs due diligence activities. Serves as a trusted advisor across the company and may be recognized as an expert [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Executive Director, Regulatory Strategy
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] regulatory leadership of programs in a therapeutic area (TA) , overseeing and directing all regulatory activities across the entire product lifecycle. Drives collaboration with crossfunctional partners (Clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Quality, Drug Safety Pharmacovigilance, Legal, Government Affairs Public Policy, Patient Advocacy) to ensure consideration of regulatory perspectives. Devotes significant time to talent and workforce development. Sets the tone for the group from a leadership perspective. Performs due diligence activities. Serves as a trusted advisor across the company and may be recognized as an expert [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Global Medical Safety PV Director
• Bern
Führungs-/ Leitungspositionen
Bavarian Nordic in Bern, Switzerland, is seeking an experienced Head of Medical Safety to provide medical leadership in Global Clinical Safety
Pharmacovigilance (GCSP) . The role involves overseeing the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical safety team, ensuring compliance with regulations, and contributing to strategic initiatives. Candidates should possess an MD degree and over 10 years of experience in clinical safety. This position offers the chance to make a significant impact in public health and advance patient [. .. ]
Job am 23.04.2026 bei Jobleads gefunden
Senior Director, Regulatory Affairs-Oncology Strategy (Remote)
Führungs-/ Leitungspositionen
[. .. ] molecule, dual-selective inhibitor of vß8 and vß1 integrins, that has shown encouraging clinical activity in the development of a treatment of immune checkpoint resistant solid tumors. Description [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Senior Director, Regulatory Affairs will report to the Vice President, Regulatory Compliance and is responsible for leading, developing and executing the global regulatory strategy for Pliants oncology programs. This involves oversight for regulatory activities across the product lifecycle, from development through post-approval, while overseeing department activities and representing Regulatory Affairs in [. .. ] medical affairs, commercial and corporate activities, including the review and submission of clinical protocols and regulatory documents, publications, investor relations/ legal public disclosures throughout the product life cycle. Support the Pharmacovigilance and Safety functions as an active member of the Safety Governance and Review team. Lead, manage, and develop a high performing team to support organizational growth as a latestage clinical organization, including providing professional and personal growth opportunities, mentorship, and change management. Provide the business development team with guidance and [. .. ]
Job am 20.04.2026 bei Jobleads gefunden
Regulatory Affairs Director
• Zürich
Führungs-/ Leitungspositionen
Role Overview The Regulatory Affairs
Director is responsible for supporting and managing EU Marketing Authorisation Applications (MAA) , lifecycle activities and lead new MAAs. The role focuses on EMA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] submissions, CTAs, authority interactions, and post-authorisation maintenance for centrally authorised medicinal products. Key Responsibilities Lead EU MAAs via the Centralised Procedure (CP) . Coordinate preparation, review, [. .. ] renewals, and commitments. Prepare and coordinate responses to Lo Q, Lo OI, and other EMA requests. Oversee labeling updates (Sm PC, PIL, labeling) for centrally authorised products. Collaborate closely with CMC, Quality, Clinical, Pharmacovigilance, and Supply Chain teams. Maintain accurate regulatory records and submission tracking in regulatory systems. Qualifications Experience Bachelors degree in Life Sciences, Pharmacy, Engineering, or related field. 10+ years experience in EU Regulatory Affairs, with strong focus on the Centralised Procedure. Proven experience with EMA MAAs and lifecycle management of centrally [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
DRUG SAFETY UNIT DIRECTOR EEA/ UK QPPV
Führungs-/ Leitungspositionen
[. .. ] diretto riporto un team di dieci Risorse. Principali Responsabilit assunzione formale del ruolo di EEA e UK QPPV, in conformit con la normativa vigente-, responsabilit legale e [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] operativa del Pharmacovigilance System; funzione di single point of contact 24/ 7 con Autorit Competenti UE, EMA, MHRA; supervisione della gestione ICRS e SUSARs, segnalazioni Eudra Vigilance e MHRA, x EVMPD e ICSR Submission Portal. Inoltre avr la responsabilit strategica e operativa della Drug Safety Unit e il coordinamento delle attivit di Farmacovigilanza a [. .. ]
Job am 03.04.2026 bei Jobleads gefunden
Medical Director, Oncology Clinical Development
• Zug
Führungs-/ Leitungspositionen
Medical
Director, Oncology Clinical Development Responsible for clinical research activities and medical dialogue for GSKs oncology antibody drug conjugate portfolio, supporting early to late stage development. Key Responsibilities Collaborate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with crossfunctional teams to develop and execute phase 13 interventional clinical trials. Develop high quality protocols aligned with the Clinical Development Plan to [. .. ] pharmacokinetics, and patient outcomes. Assume medical responsibility for trials, including patient eligibility, study design questions, and urgent safety issues. Oversee medical review of clinical trial data; collaborate with IDMC and pharmacovigilance. Participate in authoring study reports and regulatory documents; respond to health authority and ethics committee queries. Collaborate with Principal Investigators on publications (abstracts, posters, manuscripts) . Build strategic partnerships with external thought leaders. Contribute to diseasearea strategy and integrated evidence/ medical affairs teams. Engage in Oncology Clinical Developmentwide initiatives and [. .. ]
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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 28 offene Stellenanzeigen für Pharmacovigilance Director Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Director Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Pharmacovigilance Director Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Director Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Director Stellenangebote:
- Biontech (3 Jobs)
- Gilead Sciences (1 Job)
- Incyte Corporation (1 Job)
- Teva Pharmaceutical Industries Ltd. (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Director Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Director Jobs werden derzeit in Bayern (6 Jobs), Rheinland-Pfalz (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Director Jobs?
Pharmacovigilance Director Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
