54 Jobs für Drug Safety Officer
Stellenangebote Drug Safety Officer Jobs
Job vor 3 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 15.11.2025 bei Jobleads gefunden
Medical Director-Oncology, Home-Based (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The medical department consists of a Chief Medical
Officer, Medical Directors, Sr Medical Directors, Medical Writers, and
Safety Associates. The Medical Director provides medical and scientific support to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to [. .. ] project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical Activities: [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 05.11.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The medical department consists of a Chief Medical
Officer, Medical Directors, Sr Medical Directors, Medical Writers, and
Safety Associates. The Medical Director provides medical and scientific support to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to [. .. ] project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical Activities [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Medical Director Oncology, Home-Based (mwd)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview Job Overview The medical department consists of a Chief Medical
Officer Medical Directors Sr Medical Directors Medical Writers and
Safety Associates. The Medical Director provides medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and scientific support to clinical research programs study teams and investigators. The Medical Director also provides review advice and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to [. .. ] project team member: Provides medical and scientific input to clinical research programs including review of new business proposals preclinical and/or clinical data study protocols training materials informed consent Investigator Drug Brochures e CRFs analysis plan designs clinical study reports regulatory approval submissions serious and non-serious adverse event evaluation and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants etc. Supervises and manages Medical Director activities. Clinical Activities: [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Global Head of Pharmacovigilance
• Stuttgart, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a Global Head of Pharmacovigilance. 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 role directs 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 postmarketing 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 [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Essen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Dortmund, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Stuttgart, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support preclinical development activities such as target Identification, asset selection; support inlicensing, outlicensing or partnering efforts. Maintain close communication and alignment with other nonclinical development teams to ensure overall product goals. Develop and maintain scientific [. .. ]
Job am 12.10.2025 bei Jobleads gefunden
Medical Director-Oncology, Home-Based (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The medical department consists of a Chief Medical
Officer, Medical Directors, Sr Medical Directors, Medical Writers, and
Safety Associates. The Medical Director provides medical and scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to [. .. ] project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical Activities: [. .. ]
Job am 04.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Leipzig, Sachsen
Führungs-/ Leitungspositionen
[. .. ] challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutics and antibody-drug conjugates (ADCs) . With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising [. .. ] operations etc. Execute the clinical development strategy in accordance with GCP, ICH (International Conference of Harmonization) , and Competent Authority regulations. Support the Clinical Development leadership team in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team, supporting overall program safety reporting in collaboration with Patient Safety colleagues (eg provide clinical input to DSURs) . Support the Clinical Development leadership by providing medical input into the Clinical Development [. .. ] disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support pre-clinical development activities such as target Identification, asset selection; support in-licensing, out-licensing or partnering efforts. Maintain close communication and alignment with other non-clinical development teams to ensure overall product goals. [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
Global Head of Pharmacovigilance
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a Global Head of Pharmacovigilance. 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 role will direct 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 can be based on a hybrid basis from the company office in Germany or remotely. 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 risk mitigation [. .. ]
Job am 27.09.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] data presentation and discussion at national advisory boards and investigator meetings Review medical, promotional and sales training materials for scientific/ medical accuracy-provide medical review and sign-off of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical drug information letters, slides, custom responses, publications, medical education grants, and other medical affairs materials as needed Serve as an expert on call to address call center questions from healthcare professionals Define and develop required team competencies (with HR) to recruit and retain local medical team Monitor team performance in terms [. .. ] required Successful people management experience required with min 2+ years Hematology/ oncology experience required Familiarity with GCP/ ICH/ FDA requirements as well as clinical trial design, biostatistics, medical writing, product safety, and regulatory affairs Strong interpersonal, verbal and written communication skills. Strong public speaking skills Excellent leadership and management skills Ability to influence and work effectively across functions and operate in a matrix environment Ability to travel up to 30 of working time Disclaimer: The above statements are intended to describe [. .. ] 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 Executive Employment type Full-time Job function Health Care Provider Industries Referrals increase your chances of interviewing at Incyte by 2x Sign in to set [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Global Head of Pharmacovigilance
• Frankfurt (Oder) , Brandenburg
Führungs-/ Leitungspositionen
[. .. ] to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a Global Head of Pharmacovigilance. 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 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 [. .. ]
Job gestern bei Jobleads gefunden
[. .. ] of associated aviation services. Supported by 14, 000 highly skilled aviation professionals, the group is parent company to over 250+ subsidiaries. What you will do Reporting to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Chief Commercial Officer, the Base Manager will be based in Rockhampton and oversee the operational and logistical activities of the Rockhampton base. You will act as the main point of contact for internal and external stakeholders, liaise with Operations and Ground Handling teams across ports, and be located at the airport to monitor [. .. ] movements and provide on-site support to client workforces. This is a key role responsible for managing operations for a major contracted client, ensuring exceptional service delivery, and upholding the safety of all personnel. You will also lead the performance and effective management of the base and ports, ensuring safety, security, compliance, and operational standards are met while driving continuous improvement. Key Duties and Responsibilities Coordinate and respond to client requests, represent the company in stakeholder meetings, and maintain strong relationships [. .. ] contacted. Applicants must be eligible to live and work in Australia as either a citizen or permanent resident and be able to attend and successfully pass preemployment and continuing medical, drug and alcohol pathology screening. Smart Lynx Australia is committed to equal opportunity employment through fair recruitment practices. #J-18808-Ljbffr 71598809 [. .. ]
Job gestern bei Jobleads gefunden
Global Head of Pharmacovigilance
Führungs-/ Leitungspositionen
[. .. ] to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a Global Head of Pharmacovigilance. 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. The role will direct safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. It is central to ensuring safe, compliant, and successful oncology drug development and maximising patient safety from clinical trials to postmarketing surveillance. This position will report to the Chief Medical Officer and may work on a hybrid basis from the company office in Germany or remotely. 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 risk mitigation for [. .. ]
Job am 15.11.2025 bei Jobleads gefunden
Acute Care/ ER RN-Day Shift
• Minden, Nordrhein- Westfalen
[. .. ] hour Night Shift Differential 7/ hour Weekend Night Shift Differential Up to 15, 000 Signon Bonus available Tuition Assistance Flexible Scheduling Low Nurse-to-Patient Ratio Reports To Chief [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Nursing 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, signon bonus, and education assistance. Position Summary [. .. ] 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 inservice attendance records and employee practices. Maintains a clean and safe environment for patient and coworkers. Follows all general safety rules. Notified the Safety Director and/or Risk Manager of incidents involving injury or having the [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
Drug Safety Manager (gn)
• München, Bayern
Drug Safety Manager (gn) Location: Munich Department: Pharmacovigilance Start: ASAP Your Mission As a Local Safety
Officer (LSO) , you will play a key role in ensuring drug safety. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will guarantee compliance with local and global regulatory requirements and actively contribute to the continuous improvement of our European PV system. Your Responsibilities Stay ahead of regulations: Monitor local pharmacovigilance requirements, assess their impact, and keep our [. .. ]
Job am 21.10.2025 bei Jobleads gefunden
Medical Affairs Director EU ROW
• Pratteln, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] as: Medical Affairs Director EU ROW Scope of Work Reporting to the Global Head of Medical Affairs, the Medical Affairs Director EU ROW is part of the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CMO (Chief Medical Officer) organization and works closely with Clinical Development, Pharmacovigilance, Regulatory Affairs, Market Access, Marketing, and Country Medical Directors. The position supports the development and delivery of a robust medical strategy, including scientific exchange, data generation, publications, insights, and thought leader engagement, ensuring all activities uphold the highest standards of compliance and [. .. ] and in supporting HTA processes. Prior experience as medical reviewer/ approver in VEEVA. Experience in design, planning, and conduct of clinical research protocols is a plus. Knowledge and experience in Drug Safety, Regulatory, Health Economics, and/or statistical methods are a plus. Fluent English (spoken and written) ; strong ability and mandate to shape the external environment and partner effectively with internal stakeholders, especially Market Access and Marketing. Expert knowledge of the ABPI Code of Practice; recognised Thought Leader in compliance. Advanced [. .. ]
Job am 18.10.2025 bei Jobleads gefunden
Global Head of Pharmacovigilance
• Leipzig, Sachsen
Führungs-/ Leitungspositionen
[. .. ] to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a Global Head of Pharmacovigilance. 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 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 [. .. ]
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 [. .. ]
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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 54 offene Stellenanzeigen für Drug Safety Officer Jobs.
In welchen Bundesländern werden die meisten Drug Safety Officer Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Officer Jobs werden derzeit in Nordrhein-Westfalen (15 Jobs), Bayern (5 Jobs) und Baden-Württemberg (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Officer Jobs?
Drug Safety Officer Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
