31 Jobs für Drug Safety Officer
Stellenangebote Drug Safety Officer Jobs
Job vor 2 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk profile [. .. ] and non-interventional studies, as well as other data collection activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Job vor 4 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
Global Safety Project Manager-Operations Compliance (m/f/d)
• Freiburg
Homeoffice möglich
[. .. ] and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Supporting the Head [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety QPPV Office/ EU QPPV/ Graduated Plan Officer in 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 of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
• Regierungsbezirk Freiburg
[. .. ] therapeutic practice as well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. Team management of a group [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety Product Leads including l eading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk [. .. ] and non-interventional studies, as well as other data collection activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Ensuring the required quality of pharmacovigilance data Responsibility as Deputy Graduated Plan Officer according to 63a AMG which includes the following in absence of the G raduated Plan Officer: Ensuring an adequate quality management system [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Regierungsbezirk Freiburg
Führungs-/ Leitungspositionen
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including l eading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk [. .. ] and non-interventional studies, as well as other data collection activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
• Regierungsbezirk Freiburg
[. .. ] therapeutic practice as well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. Team management of a group [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety Product Leads including l eading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk [. .. ] and non-interventional studies, as well as other data collection activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Ensuring the required quality of pharmacovigilance data Responsibility as Deputy Graduated Plan Officer according to 63a AMG which includes the following in absence of the G raduated Plan Officer: Ensuring an adequate quality management system [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
Global Product Marketing Manager
• Regierungsbezirk Freiburg
[. .. ] therapeutic practice as well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. Team management of a group [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety Product Leads including l eading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk [. .. ] and non-interventional studies, as well as other data collection activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Ensuring the required quality of pharmacovigilance data Responsibility as Deputy Graduated Plan Officer according to 63a AMG which includes the following in absence of the G raduated Plan Officer: Ensuring an adequate quality management system [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
• Regierungsbezirk Freiburg
[. .. ] and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Supporting the Head [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety QPPV Office/ EU QPPV/ Graduated Plan Officer in 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 of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
IPS Powerful People
Safety Officer
• Soest
Short Description We are seeking an experienced Offshore
Safety Officer to join offshore vessel projects for our clients worldwide. If you are interested, read the description below. Function Description As [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an Offshore Safety Officer, you will be responsible for promoting and maintaining a safe working environment on offshore vessels. You will oversee health, safety, and environmental (HSE) compliance, conduct inspections, [. .. ] CPR Strong understanding of PTW (Permitto Work) systems, toolbox talks, risk assessments, and incident reporting Documentation Compliance Valid passport and offshore work authorization Seafarer s Book (for vessel-based roles) Drug alcohol clearance Experience 2-5 years of HSE experience in offshore, marine, drilling, or heavy industrial environments 77892287 [. .. ]
Job gestern bei Stellen-Online.de gefunden
Dr. Falk Pharma GmbH
• freiburg im breisgau, 79106
[. .. ] health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for:Your tasks Supporting the Head [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety QPPV Office/ EU QPPV/ Graduated Plan Officer in 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 of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Chief Executive Officer (CEO) - Maayu Mali
Führungs-/ Leitungspositionen
Chief Executive
Officer (CEO) - Maayu Mali Reports to: Board of Directors, Pius X Aboriginal Corporation About Maayu Mali: Maayu Mali is a leading Aboriginal
Drug and Alcohol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Rehabilitation Centre located in Moree, NSW. We provide culturally appropriate and holistic rehabilitation services to Aboriginal individuals and families impacted by drug and alcohol misuse. Our mission is to empower individuals to achieve lasting recovery, reconnect with their culture, and build stronger, healthier communities. About Pius X Aboriginal [. .. ] of high-quality, evidence-based, and culturally safe drug and alcohol treatment programs. Develop, implement, and monitor operational policies and procedures to ensure efficient and effective service delivery. Ensure the safety and well-being of clients and staff, maintaining a therapeutic and supportive environment. Monitor program outcomes and client progress, continuously seeking to improve service effectiveness. Manage and optimise the physical facilities and resources of Maayu Mali. Develop and manage Maayu Malis annual budget in conjunction with the Pius X Aboriginal [. .. ]
Job am 08.09.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] To continue as one of the most adaptive, effective and advanced police forces in the world, the AFP is seeking a suitably qualified professional for the role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Chief Medical Officer (CMO) . The role The CMO is the senior clinical leader for the AFP, responsible for shaping the AFPs approach to supporting the health, safety and wellbeing of our people. The role has a broad range of responsibilities across the organisation providing clinical representation both internally and across various external forums. The CMO is responsible for the strategic clinical leadership, oversees health governance, and ensures AFP members operate under evidence based, ethical and compliant medical [. .. ] areas of the AFP in support of AFP business objectives Provide Medical review services for Professional Standards including, for example, advice regarding prohibited drugs, pharmaceutical products, and alcohol and positive drug screen results. Act as a liaison with service providers when medical repatriations are required and give timely and expert advice to members unwell on posting overseas or on their return. All AFP appointees must ensure that the achievement of outcomes is in accordance with the regulatory framework, the AFP Code [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] 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: Head [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety Product Leads-Risk Label Management (m/f/d) . Responsibilities Team management of a group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Global pharmacovigilance product responsibility for the medicinal products Monitoring of the [. .. ] as well as other data collection activities including preparation and review of study-specific documents Pharmacovigilance obligations and roles Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Job gestern bei Jobleads gefunden
Chief Medical Officer
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] company focused on developing innovative therapies for patients with solid tumours. With an advancing pipeline spanning Phase I to Phase III clinical development, we are seeking an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accomplished Chief Medical Officer (CMO) to lead our global clinical and medical strategy. Reporting directly to the CEO, the CMO will be a key member of the executive leadership team and will play a central role in regulatory success, late-stage development, and value creation. Responsibilities Define and execute the overall clinical development and [. .. ] and marketing authorisation procedures. Serve as the primary medical representative in regulatory meetings, advisory committees, and interactions requiring expert medical judgment and credibility. Oversee clinical operations, medical monitoring, pharmacovigilance, and safety governance. Partner closely with Regulatory Affairs to shape regulatory strategy, briefing documents, and responses to agency questions. Engage and manage relationships with key investigators, KOLs, academic collaborators, and advisory boards. Represent the company externally at major scientific congresses, partnering discussions, and investor presentations. Build, lead, and mentor a high-performing clinical and medical organisation. Qualifications Experience MD or Md/Ph D with formal clinical training; oncology background strongly preferred. Extensive experience in oncology drug development, with senior leadership across Phase IIII clinical trials in solid tumours. Demonstrated track record of directly defending investigational or marketed oncology products with health authorities, including leading regulatory meetings and responding to complex clinical and safety questions. Proven experience supporting successful regulatory submissions (e. g. INd/CTA, MAA, NDA/ [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Global Safety Project Manager-Operations Compliance (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Responsibilities Support the Head [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Global Safety QPPV Office/ EU QPPV/ Graduated Plan Officer in 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 of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Halle (Saale) , Sachsen- Anhalt
Job Description Summary The HSE Head will be responsible for all HSE compliance aspects of a dynamic Radioligand Therapy (RLT)
drug product manufacturing plant. Job Description Key Responsibilities: As [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a member of the site leadership team, lead the creation of an injury-free work environment that protects employees from hazards (including radiation exposure) using a strong hierarchy of controls. Drive the implementation and execution of the HSE roadmap defined by the company, working closely with all functions within the site and the broader Novartis organization. Function as the Site Radiation Safety subject matter expert and collaborate with operations and technical teams to safely manage radioactive materials from raw materials to finished product and waste disposal. Maintain knowledge of and ensure strict adherence to all applicable regulatory compliance standards including Radiation Safety, Governance, Business Continuity Emergencies Management and Environmental Health and Safety. Coordinate timely application and renewals for all required HSE permits to ensure continuous operations and support all regulatory inspections and audits. Serve as the site Radiation Safety Officer and collaborate with the operations and technical teams to safely manage radioactive materials from raw materials to product and waste. Support Project Manager in the development of the project specific HSE Strategy, selection of competent team members, determination of competency of planned/assigned resources (internal and external) and ensuring that [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
HSE Head
• Halle (Saale) , Sachsen- Anhalt
Summary The HSE Head will be responsible for all HSE compliance aspects of a dynamic Radioligand Therapy (RLT)
drug product manufacturing plant. About The Role Key Responsibilities: As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of the site leadership team, lead the creation of an injury-free work environment that protects employees from hazards (including radiation exposure) using a strong hierarchy of controls. Drive the implementation and execution of the HSE roadmap defined by the company, working closely with all functions within the site and the broader Novartis organization. Function as the Site Radiation Safety subject matter expert and collaborate with operations and technical teams to safely manage radioactive materials from raw materials to finished product and waste disposal. Maintain knowledge of and ensure strict adherence to all applicable regulatory compliance standards including Radiation Safety, Governance, Business Continuity Emergencies Management and Environmental Health and Safety. Coordinate timely application and renewals for all required HSE permits to ensure continuous operations and support all regulatory inspections and audits. Serve as the site Radiation Safety Officer and collaborate with the operations and technical teams to safely manage radioactive materials from raw materials to product and waste. Support Project Manager in the development of the project specific HSE Strategy, selection of competent team members, determination of competency of planned/assigned resources (internal and external) and ensuring that [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Ershausen/ Geismar, Thüringen
[. .. ] be part of a team that contributes to a culture that positively impacts the communities and customers we serve. Job Description LOCATION: Geismar, LA SITE: Petroleum plant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] POSITION: TWIC Security Officer PAY: 16.00/ hour/ pays weekly SHIFT: 12-hr shifts MUST HAVE BADGING AND ACCESS CONTROL EXPERIENCE AND ADVANCE COMPUTER KNOWLEDGE Qualifications ABLE TO PASS BACKGROUND AND DRUG SCREEN (DISA) ACTIVE TWIC CARD (NO RECEIPTS) LOUISIANA DRIVERS LICENSE ADVANCE COMPUTER SKILLS AND COMFORTABLE USING A TABLET OR COMPUTER ABLE TO STANd/WALK FOR EXTENDED PERIODS ABLE TO WORK OUTDOORS IN THE ELEMENTS High school diploma or equivalent required; at least 21 years of age Licensing requirements are subject [. .. ] Ensure the facility is provided with high quality security services to protect people and property. Maintains proficiency in the use of all assigned protective equipment, restraint devices and weapons. Report safety concern, security breaches and unusual circumstances both verbally and in writing. Preserves order and acts to enforce regulations and directives for the site pertaining to personnel, visitors and premises. Monitors closed circuit television systems and alarms; Reports safety concerns, security breaches and unusual circumstances both verbally and in writing. Maintains [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
Supervisory Engineer, GS-08XX-13 (57557)
• Ansbach, Bayern
Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten
[. .. ] to the provisions of the Joint Travel Regulations. Incentives are not authorized. Appointment Type: Permanent Work Schedule: Full-time Service: Competitive Promotion Potential: 13 Supervisory Status: Yes Security [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clearance: Secret Drug Test: Not required Financial Disclosure: Yes Position Summary Assigned as Resident Engineer or Chief of a significant Project Office, responsible for the administration and management of construction work assigned. Ensures timely and economical execution; proper quality and quantity of materials, equipment, and workmanship; adequacy of contractors methods and operations; and that all work is carried out in accordance with plans and specifications. Work is performed by direct contract, troop construction, or indirect contracts through the Host Nation. Acts as Contracting Officer Representative (COR) or Administrative Contracting Officer (ACO) with specific authorized delegations. Duties Supervises the work of approximately 512 subordinate employees engaged in the overall management and surveillance of assigned construction projects. Plans and assigns work, establishing priorities and deadlines, considering the relative difficulty of the work and capabilities of employees. [. .. ] as progress payments, contract modification, delays in construction, etc. , as related to field construction activities. Conduct review of plans for conformance to Department of Defense standards, project criteria, and safety codes. Other Conditions And Requirements One-year trial/ probationary period may be required. Appointment may be subject to a suitability or fitness determination, as determined by a completed background investigation. This position requires you to submit a Confidential Financial Disclosure Report (OGE450) upon entry, and annually thereafter. Male applicants born [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
• Minden, Nordrhein- Westfalen
[. .. ] Shift Differential 7/ hour Weekend Night Shift Differential Up to 15, 000 Sign-on Bonus available Tuition Assistance Flexible Scheduling Low Nurse-to-Patient Ratio Reports To : Chief Nursing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Officer Expectations: RN will be responsible for Med/Surg, Swing Bed (Skilled) , and ER patient flow. BLS, ACLS, PALS, and TNCC certifications will be required within one year of employment if not already obtained. Incentives: Competitive wage and benefit package including shift differentials, sign-on bonus, and education assistance. Position [. .. ] of medications during administration to patients. Reports the potential for unsafe medication delivery/ harm using Incident Trackers medication error form. Works in collaboration with e Pharmacy and medical staff to calculate drug doses and drip rates in order to administer appropriate doses of medications to patients. Organization Establishes priorities and organizes work for efficient delivery of patient care. Demonstrates ability to adapt to changes in work load or patient assignments. Computer Skills Generation of MAR, documentation in MAR Patient admissionable to admit [. .. ] Demonstrates correct hand washing technique. Demonstrates knowledge of appropriate personal protective equipment (PPE) and uses same in practice. Notifies the Infection Control Nurse of real or potential exposures. Risk Management Safety Program Demonstrates adherence to risk management and safety policies and codes as evidenced by in-service attendance records and employee practices. Maintains a clean and safe environment for patient and co-workers. Follows all general safety rules. Notified the Safety Director and/or Risk Manager of incidents involving injury or [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Senior Medical Director, Early Clinical Development
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] through transition to registrational studies) . Essential Functions Of The Job (Key Responsibilities) Leads development efforts for assets post-candidate selection through first in human trials, including early [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] dose escalation, safety and tolerability evaluation, dose selection, translational medicine (proof of mechanism studies) and proof of concept studies in human (ph 1 or 2) . Participates in asset/ portfolio strategies and prioritization, internal and external messaging, governance, and cross-functional interface with all key stakeholders, including translational science, clinical pharmacology and pharmacometrics, [. .. ] 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. Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans. Collaborates with external vendors such as CROs, external imaging and laboratory vendors for [. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for 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 09.10.2025 bei Jobleads gefunden
HSE Head
• Rasch, Bayern
Summary The HSE Head will be responsible for all HSE compliance aspects of a dynamic Radioligand Therapy (RLT)
drug product manufacturing plant. Summary The HSE Head will be responsible [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for all HSE compliance aspects of a dynamic Radioligand Therapy (RLT) drug product manufacturing plant. About The Role Key Responsbilities: As a member of the site leadership team, lead the creation of an injury-free work environment that protects employees [. .. ] the implementation and execution of the HSE roadmap defined by the company, working closely with all functions within the site and the broader Novartis organization. Function as the Site Radiation Safety subject matter expert and collaborate with operations and technical teams to safely manage radioactive materials from raw materials to finished product and waste disposal. Maintain knowledge of and ensure strict adherence to all applicable regulatory compliance standards including Radiation Safety, Governance, Business Continuity Emergencies Management and Environmental Health and Safety. Coordinate timely application and renewals for all required HSE permits to ensure continuous operations and support all regulatory inspections and audits. Serve as the site Radiation Safety Officer and collaborate with the operations and technical teams to safely manage radioactive materials from raw materials to product and waste. Support Project Manager in the development of the project specific HSE Strategy, selection of competent team members, determination of competency of planned/assigned resources (internal and external) and ensuring that [. .. ]
Job am 27.09.2025 bei Jobleads gefunden
Global head of pharmacovigilance
• Thüringen
Führungs-/ Leitungspositionen
[. .. ] Join a multidisciplinary, highly focused group working to deliver promising ADCs to patients with solid and haematological cancers. Role and responsibilities This is a strategic leadership role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. This will be responsible for directing safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and [. .. ]
Neu Job vor 6 Std. bei Neuvoo gefunden
Freelancer Muskan Malik
Medical Professionals apply for Overseas
Freiberuflich
[. .. ] and monitor patient conditions. Administer medications and injections as prescribed. Assist doctors in medical procedures and surgeries. Provide emotional support to patients and families. Maintain accurate medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] records and follow safety protocols. Skills Required Nurse Practitioners, Medical Doctor, Doctorate, Registered Nurse, Doctor Activities, Medical Services, Nurse Assistant, Doctors, Medical Officer, Staff Nurse, Doctor, Medical, Drug Regulatory Doctor, Nurse, Male Nurse, Medical Affairs 79854640 [. .. ]
Neu Job vor 6 Std. bei Neuvoo gefunden
Vijay Sabarwal (Proprietorship of Advance Immigration Solutions)
Medical Professionals Jobs In Abroad Countries
[. .. ] and monitor patient conditions. Administer medications and injections as prescribed. Assist doctors in medical procedures and surgeries. Provide emotional support to patients and families. Maintain accurate medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] records and follow safety protocols. Skills Required Nurse Practitioners, Medical Doctor, Doctorate, Registered Nurse, Doctor Activities, Medical Services, Nurse Assistant, Doctors, Doctor, Medical Officer, Staff Nurse, Nurse Aide, Medical, Drug Regulatory Doctor, Nurse, Male Nurse, Medical Affairs 79855886 [. .. ]
Job gestern bei Neuvoo.com gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
Führungs-/ Leitungspositionen
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk profile [. .. ] and non-interventional studies, as well as other data collection activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term 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 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Drug Safety Officer pro Jahr?
Als Drug Safety Officer verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Drug Safety Officer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 31 offene Stellenanzeigen für Drug Safety Officer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Officer Jobs?
Aktuell suchen 7 Unternehmen nach Bewerbern für Drug Safety Officer Jobs.
Welche Unternehmen suchen nach Bewerbern für Drug Safety Officer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Safety Officer Stellenangebote:
- Dr. Falk Pharma GmbH (11 Jobs)
- Commonwealth of Virginia (3 Jobs)
- IPS Powerful People (1 Job)
- Freelancer Muskan Malik (1 Job)
- U. S. Army Europe and Africa (1 Job)
In welchen Bundesländern werden die meisten Drug Safety Officer Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Officer Jobs werden derzeit in Niedersachsen (9 Jobs), Baden-Württemberg (5 Jobs) und Bayern (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Officer Jobs?
Drug Safety Officer Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
