Drug Safety Specialist Stellenangebote

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Stellenangebote Drug Safety Specialist Jobs bei Stellen-Online

Job vor 14 Tagen gefunden Miltenyi Biomedicine GmbH

IMP Manager- Clinical Trials (m f d) - Homeoffice, Vollzeit

• 51429, Bergisch Gladbach, 51429 Homeoffice möglich

MEHR

[...] while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T- cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. Job Description In the Clinical Trial Execution Service department you will support our [...] compliant supply of fresh and frozen IMP, including documentation in accordance with regulatory requirements. This includes monitoring the lifecycle of IMP and comparator products from receipt to destruction, including labelling design, packaging, IWRS (Interactive Response Technology) set- up, distribution and drug accountability. As the orchestration of logistics processes is critical to the product flow of our CAR- T clinical trials, you [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, and staff [...]
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Stellenangebote Drug Safety Specialist Jobs bei StepStone

Job vom 17.11.2024 EXTEDO GmbH Marketing Specialist/ Marketing Manager (m/f/d) B2B • Ottobrunn bei München Homeoffice möglich

MEHR

[...] that medicines and vaccinations reach where they are needed faster and, at the same time, more safely: with the patients. Regulatory authorities around the world also rely on us to review submissions and ensure they meet the highest standards of drug safety. For our location in Ottobrunn near Munich we are actively seeking a Marketing Specialist/ Marketing Manager (m/f/d) B2B Support the team to draft a yearly marketing plan, including an estimated budget Plan and conduct [...]
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Stellenangebote Drug Safety Specialist Jobs bei JobMESH

Job vom 06.12.2024 Miltenyi Biomedicine GmbH

IMP Manager- Clinical Trials (m f d)

• North Rhine- Westphalia

MEHR

[...] while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T- cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. Job Description In the Clinical Trial Execution Service department you will support our [...] compliant supply of fresh and frozen IMP, including documentation in accordance with regulatory requirements. This includes monitoring the lifecycle of IMP and comparator products from receipt to destruction, including labelling design, packaging, IWRS (Interactive Response Technology) set- up, distribution and drug accountability. As the orchestration of logistics processes is critical to the product flow of our CAR- T clinical trials, you [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, and staff [...]

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Stellenangebote Drug Safety Specialist Jobs bei Neuvoo

Job vom 02.12.2024 ABS Biotechnologies GmbH Technical Specialist- Biology Laboratory (Full time; 40 hours per week) • Tulln, Austria

MEHR

We are offering an exciting opportunity for a Technical Specialist to join ABS Biotechnologies GmbH. Our mission is to use next- generation stem cell technology for rigorous screening of new drug compounds, this prevents exposing patients to harmful side effects This position is primarily laboratory based Perform cell culture (media change, [...] requirements Provide administrative support for the laboratory Supporting various scientific projects by ensuring smooth laboratory operations, including sample management Participate in technical staff training as needed Maintain general order, cleanliness, and sterile work in biosafety cabinets, strict adherence to occupational safety regulations Holds a bachelors or masters degree (or equivalent) in a life science field Has practical experience in a laboratory [...]

Stellenangebote Drug Safety Specialist Jobs bei Jobleads

Job gestern gefunden

Senior Test Automation Specialist

MEHR

[...] believe together, anything is possible. Use sophisticated technology to deliver everyday essentials and natural resources for Australia s biggest companies. Work with major customers in retail, healthcare, government and defence. Shape the future of logistics with industry- leading innovations in safety, sustainability, and efficiency. Create a career to be proud of. Expect all this and more when you join Linfox. What does the job look like? As the Senior Test Automation Specialist on a 12- month contract, you will play a pivotal role in designing, implementing, and maintaining advanced automation frameworks and [...] end of year break, please expect an update during the week commencing January 6th. You will be required to meet Linfoxs employment criteria which will include but not be limited to a criminal history check and full medical with a drug and alcohol test. To find out more about opportunities at Linfox, visit www. linfox. com/ careers . #J- 18808- [...]

Job vor 2 Tagen gefunden Postdoctoral Scientist- Metabolomics Specialist for Drug Safety- all genders- (Fixed- term. . . • Frankfurt, Hesse

MEHR

About the job Our Team: At Sanofi, we leverage advanced technologies to accelerate R D for patients and enhance patient safety throughout the entire research and development process. Join our Digital Toxicology team as a Postdoctoral Scientist specializing in Metabolomics for Drug Safety, and youll be at the forefront of this exciting field. Your role will involve leading, developing, and applying innovative [...]
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Job vor 2 Tagen gefunden

Executive Director Clinical Development

• Dortmund, Nordrhein- Westfalen Führungs-/ Leitungspositionen

MEHR

[...] for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release [...] Trial Protocols and Pediatric Development Plans together with your cross- functional project teams. Mentor a team of Clinical Program Leads. You also provide input to Project Analysis Data Management Plans, Company Core Data Sheet, Annual Safety Report/ IND (Investigational New Drug) Safety Reports. Thanks to your expertise, you provide medical leadership in regulatory meetings and support submission strategy, regulatory dossiers and [...] (s) , e. g. , Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]

Job vor 2 Tagen gefunden VP Clinical Development • Dortmund, Nordrhein- Westfalen

MEHR

[...] for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release [...] Core Clinical Trial Protocols and Pediatric Development Plans together with your cross- functional project teams. Mentor a team of Clinical Program Leads. Provide input to Project Analysis Data Management Plans, Company Core Data Sheet, Annual Safety Report/ IND (Investigational New Drug) Safety Reports. Provide medical leadership in regulatory meetings and support submission strategy, regulatory dossiers and safety issues. Maintain an external [...] designated asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]

Job vor 2 Tagen gefunden

VP Clinical Development

• Leipzig, Sachsen

MEHR

[...] for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release [...] Core Clinical Trial Protocols, and Pediatric Development Plans together with your cross- functional project teams. Mentor a team of Clinical Program Leads. Provide input to Project Analysis Data Management Plans, Company Core Data Sheet, Annual Safety Report/ IND (Investigational New Drug) Safety Reports. Provide medical leadership in regulatory meetings and support submission strategy, regulatory dossiers, and safety issues. Maintain an external [...] asset (s) , e. g. , Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees, and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]

Job vor 4 Tagen gefunden INTELLIGENCE SPECIALIST • Ramstein- Miesenbach, Rheinland- Pfalz

MEHR

[...] for access to Sensitive Compartmented Information (SCI) , other intelligence- related Special Sensitive information, or involvement in Top Secret Special Access Programs (SAP) to fully perform the duties and responsibilities of the position. A non- disclosure agreement must be signed. Drug Testing: This position has been designated by the Air Force as a Testing Designated Position (TDP) under the Air Force Civilian Drug Demand Reduction Program. Employee must pass initial and periodic short notice drug testing. Illegal drug use by employees in sensitive positions presents a clear threat to the mission of the Air Force, national security, and public safety. PART- TIME OR UNPAID EXPERIENCE: Credit will be given for appropriate unpaid and or part- time work. You must clearly [...]
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Job vom 06.12.2024

Head Medical Safety Operations (m/f/d)

MEHR

[...] and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally. Join us as a Founder of our new Sandoz Your Key Responsibilities: Manages and coaches a team of Medical Safety Experts/ Specialist/ Associates. Manages the strategic planning of the activities delivered by the Medical Safety Experts/ Specialist/ Associates. Provides strategic leadership within [...] guidance on processes to the Countries and regions Patient safety organization as well as other functions outside Medical Safety. Responsible for oversight of metrics in scope of Medical Safety Operations. What you ll bring to the role: 6 years in drug development in a major pharmaceutical company (of which 5 are in a global position in safety/ clinical/ medical affairs or [...]

Job vom 02.12.2024 Head Medical Safety Operations (m/f/d) • Holzkirchen, Bayern

MEHR

Job Description Summary Designs develops safety surveillance strategy for products and approval. Responsible for the company s drug surveillance program including the necessary follow- up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety [...] with governmental regulations. Provides and contributes trending and safety signal detection and risk management assessment for the products life cycle. Provides safety support to the clinical development teams. Your Key Responsibilities: Manages and coaches a team of Medical Safety Experts/ Specialist/ Associates. Manages the strategic planning of the activities delivered by the Medical Safety Experts/ Specialist/ Associates. Provides strategic leadership within [...]

Job vom 26.11.2024

Head of Development

Führungs-/ Leitungspositionen

MEHR

[...] the renewable energy industry will be pivotal in leading multidisciplinary teams to optimize asset development to de- risk projects and maximize value for the Group. Your duties and responsibilities will include: Lead all project workstreams, including stakeholder engagement, approvals, health safety environmental, land acquisition, grid connections, financial feasibility, and more. Manage development budgets, resources, and schedules to ensure efficient project delivery. [...] ability to develop strategic directions. Please note that relevant screening checks will be conducted as part of the recruitment process. These may include a national criminal history check and a requirement for you to undergo pre- employment medical assessment including drug and alcohol screen. What we offer UGL promotes diversity and alternate ways of working including part- time. When you join [...] A Strong Health and Safety Culture Dedicated Wellness Program Paid Parental Leave Educational and leadership development opportunities Access endless career options and pathways through the CIMIC Group #UGLNew Energy #UGL Resources Projects #unitewiththeverybest UGL is CIMIC Groups specialist end- to- end engineering, services and operations provider, with a rich history dating back to 1899 and now a market [...]
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Job vom 15.11.2024 VP Clinical Development

MEHR

[...] for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release [...] Clinical Trial Protocols and Pediatric Development Plans together with your cross- functional project teams. Mentor team of Clinical Program Leads You also provide input to Project Analysis Data Management Plans, Company Core Data Sheet, Annual Safety Report/ IND (Investigational New Drug) Safety Reports. Thanks to your expertise, you provide medical leadership in regulatory meetings and support submission strategy, regulatory dossiers and [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]

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