35 Jobs für Drug Safety Manager
Stellenangebote Drug Safety Manager Jobs
Job vor 6 Tagen bei Mindmatch.ai gefunden
Öffentlicher Dienst Verbände Karriere
• Hamburg, HH
Allergopharma Gmb H Co. KG mit Sitz in Reinbek gehört zum Unternehmensverband der Dermapharm AG und ist ein international agierendes Pharmaunternehmen, das sich auf die Entwicklung, Herstellung und den Vertrieb [...]
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[...] von Präparaten zur Diagnose und Therapie allergischer Erkr. . . 90524498 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Allergopharma GmbH Co. KG
Drug Safety Manager (m/w/d)
• Stormarn; Schleswig- Holstein Reinbek, DE
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten Jobticket 30+ Urlaubstage
[. .. ] Entwicklung, Herstellung und den Vertrieb von Präparaten zur Diagnose und Therapie allergischer Erkrankungen spezialisiert hat. Wir suchen zum nächstmöglichen Zeitpunkt unbefristet und in Vollzeit in Reinbek bei [...]
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[...] Hamburg eine/n Drug Safety Manager (m/w/d) Aufgaben Erfassung, Bewertung, Meldung und Nachverfolgung von unerwünschten Arzneimittelwirkungen sowie die dazugehörige Dateneingabe in der globalen Safety Datenbank Verantwortung für die regelmäßige Literaturrecherche (global und lokal) , die Erstellung von periodischen Sicherheitsberichten, der Detektion von Signalen im Rahmen des kontinuierlichen Signalmanagements und die Erstellung von Nutzen-Risiko-[. .. ]
Job am 29.03.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] and/or support cross-functional teams to design and execute clinical development plans from Phase 1 through Phase 2 (proof-of-concept) Coach Clinical Scientists in a line-or functional-
manager status Closely [...]
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[...] interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research and biomarker groups and other members of project teams Lead and/or support internal stakeholder management and governance interactions around project plans and therapeutic area strategy Lead and/or support external engagements with advisory boards, site investigators, health authorities, and other key stakeholders [. .. ] a similar field. Board certification and fellowship training or research experience in relevant areas is preferred You bring at least 5 years of experience in longitudinal clinical research, preferably in drug development or clinical trials. You hold a strong track record of scientific excellence in the field, evidenced by substantial achievement in designing and implementing clinical trials and/or a high level of scholarship in industry or academia You have experience in clinical drug development within the industry, ideally in the [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Veeva Systems
Engagement Manager-R D Business Consulting
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] consulting working together. We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen. The Role [...]
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[...] As an Engagement Manager in our R D Business Consulting practice, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI. You will focus on reshaping operating models, driving organizational change, and measuring tangible business value. R D Business Consulting supports biopharma, medtech, animal and [. .. ] Sciences Consulting (Business or Management Consulting preferred) Leadership: Proven track record of managing large project teams and 1M+ engagements Domain Knowledge: Proven expertise in Clinical Data/ Operations, Regulatory or Pharmacovigilance/ Drug Safety and the broader Life Sciences industry Mindset: A highly analytical approach to problem-solving with the ability to influence C-suite stakeholders Education: Bachelors degree or higher Nice to Have Deep knowledge of Veeva products Experience delivering Saa S or Tech-enabled consulting solutions The Process Our process is different than [. .. ]
Job vor 2 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
Senior CRA Germany Oncology Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
drug development [...]
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[...] and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case [. .. ] off visits for junior CRA staff, as assigned. May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL) , or operational line manager. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Experience as a CRA in oncology trials. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, [. .. ]
Job am 25.04.2026 bei Jooble gefunden
Clinical Trial Manager
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Trial
Manager Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
drug development and [...]
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[...] commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and [. .. ]
Job am 15.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Sr CRA Oncology Germany Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
drug development [...]
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[...] and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case [. .. ] off visits for junior CRA staff, as assigned. May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL) , or operational line manager. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Three years monitoring experience Experience in monitoring oncology trials Must demonstrate good computer skills and be able to embrace new technologies [. .. ]
Job am 08.04.2026 bei Jooble gefunden
HARMAN International
Software Architect, Connectivity (m/f/d)
• Region Donau- Iller, Württemberg; Regierungsbezirk Tübingen; Württemberg Ulm, DE
Work-Life-Balance
[. .. ] security and regulatory compliance objectives Document key technical requirements for our Telematic Software Customer contact for identifying and understanding architectural requirements Contribute to the Cybersecurity project efforts [...]
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[...] Support the Cybersecurity Manager in developing different technical work products Represent the project for Threat Analysis and Risk Assessment (TARA) Make risk treatment decisions Derive security requirements from TARA, and maintain the requirements specification for the cybersecurity concept Support RFI/ RFQ response on cybersecurity activities What You Need Master s or Bachelor s degree [. .. ] to understand customer wishes, make decisions, communicate these decisions, and control the technical direction of the project What is Nice to Have Experience with infotainment systems Knowledge of Automotive Functional Safety (ISO 26262) . Competent in Automotive Cybersecurity Engineering (ISO 21434) Competent in TARA methodologies Knowledge of cryptography applications in the automotive ecosystem Knowledge of secure coding standards. Experience in AUTOSAR, especially with AP, is a plus Knowledge of process models (e. g. Automotive SPICE, especially SWE. 1 SWE. 2) What [. .. ] necessities Be willing to work in an office, with hybrid model of remote and onsite office in one of our major software development sites Successfully complete a background investigation and drug screen as a condition of employment What We Offer HARMAN offers a diverse and inclusive work environment that fosters and encourages career development opportunities, professional training and competitive market base compensation You will also receive top-notch employee discounts on Harmans Consumer Audio (JBL, AKG, HARMAN Kardon) and Samsung products [. .. ]
Job am 08.04.2026 bei Jooble gefunden
IQVIA
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Führungs-/ Leitungspositionen
The Sr. CDM will lead and contribute to data management activities in support of Client s studies across all stages of clinical
drug development. Summary of Key Responsibilities Contribute [...]
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[...] to data management activities as a lead study data manager in support of Client s clinical studies Lead database build activities including leading cross-functional review of e CRF content, review of edit check specifications, and perform user acceptance testing Monitor data collection, coding, and cleaning by vendors through tracking of study metrics and targeted data reviews Oversight of database lock activities and ultimate archiving of study data Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory Affairs; CROs, central and local laboratories, and other vendors Establish cross-functional, internal data review plans, coordinate data cuts/ transfers, and conduct data reviews Review CRO data management plans, CRF completion guidelines, external data transfer specifications and other study documentation Contribute to development and implementation [. .. ]
Job am 08.04.2026 bei Jooble gefunden
JSAN
Driver
• Region Donau- Iller, Württemberg; Regierungsbezirk Tübingen; Württemberg Ulm, DE
[. .. ] able to reach the roof of the vehicle and vehicle mount assembly (able to use a short step ladder to access camera) MUST be able to pass [...]
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[...] a 5 Panel Drug Screen or Oral Fluid Drug Screen as law permits MUST be familiar with GPS devices and understand that telematics are used to monitor driving style and provide safety feedback. Have experience with android devices, to include cell phones and tablets, and should be technically savvy. Understand basic computer skills and be able to write legible emails. Ability to communicate clearly. Ability to remain calm in stressful driving situations (e. g. at rush hour) Have some level of expertise [. .. ] navigation software and other applications as instructed to follow routes. Work effectively as part of a larger mapping team. Follow the rules and work missions as requested by the Project Manager. Complete daily checks on the vehicle and equipment and notify manager of any issues. Operate carefully especially with the regards to the equipment on the vehicle, such as knowledge of the height of the vehicle with the equipment, being mindful of low-hanging objects such as trees. Protect the equipment [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Veeva Systems
• Berlin Berlin, DE
[. .. ] our leading R D consulting practice is a strategic priority for Veeva, with high visibility within the company and to leaders of the wider Life Sciences industry. [...]
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[...] As an Engagement Manager, you will manage complex and novel consulting projects for Veeva customers in the research and development (R D) space managing teams and planning, organizing, and tracking all aspects of delivery. You will support building our brand in the market, developing our customer network, and identifying and acquiring new projects to [. .. ] our customers to deliver on their complex business challenges. As part of the team, you will focus on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/ Drug Safety, and Quality Management. What You ll Do Lead multiple project engagement teams empowering the team to plan and manage all aspects of delivery, from scope to quality assurance Be responsible for the end-to-end design, build, and delivery of deliverables that meet overall project goals and objectives Proactively lead [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Local Clinical Trial Manager-Single Sponsor
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Local Clinical Trial
Manager-Single Sponsor Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the [...]
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[...] drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] single sponsor clients we are looking for CTM to cover phase II/ III trials. Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Job Title: Environmental Program
Manager II Location: Remote, USA with strong preference to candidates in Arkansas, Louisiana, New Mexico, Oklahoma, or Texas Job Summary The Program Manager II is [...]
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[...] responsible for leading and managing the companys Environmental Protection Agency (EPA) contracts within EPA Region 6 and other regions and ensuring all projects are executed in [. .. ] Address and resolve project issues and challenges, including navigating complex client and team dynamics. Serve as a Senior Project Manager. Uphold contract and company required QA/ QC and Health and Safety standards. Client and Stakeholder Engagement Serve as the liaison with EPA clients, fostering strong relationships to ensure satisfaction and repeat business. Coordinate with external stakeholders for scope and cost sensitive items including EPA clients and state and local agencies as needed for specific projects. Respond to client inquiries and proactively [. .. ] may require longer hours and weekends. Office type: Remote; candidate should reside within EPA Region 6 (Arkansas, Louisiana, New Mexico, Oklahoma, or Texas) . Travel: 10 per year. Pre-hire drug test required. All positions are subject to a pre-hire education and driving record verification. This specific role supports a U. S. Federal government contract which requires employees engaged on this contract to be U. S. citizens. EEO Statement We are an Equal Opportunity employer. All applicants will receive consideration [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Cyber Security Lead-OT
Job Summary The Cyber Security
Manager (Operational Technology) is a seniorlevel, handson technical leader responsible for designing, implementing, and maintaining advanced OT cybersecurity architectures across critical energysector environments. The [...]
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[...] role focuses on secure OT network design, hardening of controlsystem platforms, and guiding engineering and operations teams in deploying resilient security controls. The manager leads OT security [. .. ] ICS/ SCADA protection, asset visibility, endpoint security, and threat detection. The position also supports essential governance activities, ensuring alignment with NIST frameworks and NERCCIP requirements while balancing operational reliability and safety. The role collaborates closely with engineering, operations, compliance, and SOC teams and may oversee contractors, vendors, or project teams. Occasional travel to operational sites may be required. Job Responsibilities Design, implement, and maintain secure OT network architecture aligned with the Purdue Enterprise Reference Model. Lead segmentation and zoning initiatives to [. .. ] Employment Policies PSEG is not offering visa sponsorship for this position. Employees may be required to perform extended hours or work on unfamiliar sites during storm or outage restoration efforts. Drug and alcohol testing is required for all roles, including preemployment, for cause, and postincident testing. Employees in federally regulated roles are subject to random testing, inclusive of marijuana; CBD product use may result in a positive test and is not a legitimate medical explanation. Equal Opportunity Accommodations PSEGLI is an [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] Optimize geographic allocation of internal resources and external partnerships to balance speed, quality, cost, and risk across the portfolio. Oversee proactive site management and monitoring strategies, ensuring [...]
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[...] data integrity, patient safety, and regulatory compliance. Strengthen BMSs position as a preferred sponsor by driving effective site engagement, understanding site dynamics, and addressing operational pain points. Demonstrate enterprise leadership and the ability to form productive relationships across the organization. Understand regulatory environment within each region, providing direction, guidance, and support during inspection preparation, sponsor and site activities. Qualifications Experience Advanced degree preferred; minimum 15 years of relevant industry experience. Strong understanding of the drug development process with proven expertise in clinical trial execution and management in a global arena. Expert in ICH/ GCP principles as it relates to clinical trial execution. Direct experience in working with and managing CRO partnerships. Diverse technical expertise to be a credible interface to global development and business partners. [. .. ] life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Paid time off for US exempt employees: unlimited with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio) , and optional holidays as applicable. Standard paid vacation: 160 hours annual paid vacation for new hires (with manager approval) , 11 national holidays, and 3 optional holidays. Additional time off includes unlimited paid [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Production Manager 3rd Shift
• Stuttgart, Baden- Württemberg
[. .. ] Come, stay, and grow with us. What Drives Success This role is responsible for developing, executing, and maintaining fabrication operations to ensure all products meet customer demand, [...]
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[...] quality standards, and safety expectations. The position will drive long-term strategies to improve operational performance, aligning manufacturing processes with Quality Assurance objectives while supporting Lean and Six Sigma initiatives. This role partners cross-functionally to implement continuous improvement strategies across the organization. Responsibilities Develop, implement, and sustain fabrication and assembly operations to meet [. .. ] this role are not eligible for overtime. Benefits : Subject to applicable eligibility requirements, the following benefits are offered for this role: tuition reimbursement; medical, dental, and vision insurance; prescription drug coverage; 401 (k) retirement plan; short-term disability insurance; 8 weeks paid birthing leave; 2 weeks paid bonding leave; life and long-term disability insurance. Depending on date of hire, and subject to applicable eligibility requirements, new employees in this role also receive up to: 12 days paid time off, [. .. ]
Job am 22.04.2026 bei Jobleads gefunden
Sabbaticals
[. .. ] full potential. We want you to have a sense of belonging and feel valued for your contributions and the perspectives you bring. Summary The primary responsibility of [...]
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[...] the Pre-Construction Manager is to lead and manage pre-construction activities from an initial opportunity through to construction kickoff on RES 3rdparty construction opportunities, effectively standing in and acting as the project manager until the opportunity is secured and fully handed over to the selected execution team. Duties of the Pre Construction Manager [. .. ] preconstructionrelated work, including geotechnical and geophysical investigation, topographical survey mapping, and utility location/ service surveys. Coordinates preconstruction site access and site conditions/ constructability reviews and reporting. Includes compliance with RES safety program for preconstruction activities. Follows safety and security procedures, determines appropriate action, reports potentially unsafe conditions, and adequately uses materials and equipment. Ensures the site is ready for mobilization. Standardization Complies with preconstruction processes and procedures with Stage Gate requirements. Partners with the project Kickoff process and procedures. Identifies areas [. .. ] extreme cold, heat, and humidity, wet climates, noise, and hazards in the working environment. We maintain a drugfree workplace. Candidates will be required to pass a preemployment background investigation and drug test as a condition of employment. Equal Opportunity Statement RES is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other [. .. ]
Job am 22.04.2026 bei Jobleads gefunden
Senior Manager Human Resources Business Partner ( Remote New Jersey Based )
COMMUNITY NAME Community Support Office Job ID 2026-240423 JOB OVERVIEW The Senior
Manager Human Resources Business Partner (HRBP) serves as a strategic advisor and thought partner to Regional Field [...]
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[...] Leadership, aligning human capital strategies with organizational objectives, supporting our communities and geographically dispersed employees across the U. S. This role leads both regional and enterprise-wide initiatives in talent management, organizational effectiveness and [. .. ] position, plan/ program offered by Sunrise at the time, and required performance pursuant to the plan/ program. Some benefits have eligibility requirements PRE-EMPLOYMENT REQUIREMENTS Sunrise considers the health and safety of its residents, family members, and team members among its highest priorities. Employment with Sunrise is contingent upon completing and passing a drug test (which does not include marijuana) and Tuberculosis Test, and a physical evaluation and a background check where required. Covid-19 and Influenza vaccination may be required if mandated by applicable federal, state, and local laws and authorities. COMPENSATION DISCLAIMER Selected candidates will be offered competitive compensation based on geographic [. .. ]
Job am 21.04.2026 bei Jobleads gefunden
[. .. ] this top culture and workplace designation, highlighting the special place Sunrise is to be a part of. COMMUNITY NAME Community Support Office Job ID 2026-240422 JOB OVERVIEW [...]
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[...] The Senior Manager Human Resources Business Partner (HRBP) serves as a strategic advisor and thought partner to Regional Field Leadership, aligning human capital strategies with organizational objectives, supporting our communities and geographically dispersed employees across the U. S. This role leads both regional and enterprise-wide initiatives in talent management, organizational effectiveness and [. .. ] plan/ program. Some benefits have eligibility requirements Apply today to learn why Sunrise Senior Living is a certified Great Place to Work PRE-EMPLOYMENT REQUIREMENTS Sunrise considers the health and safety of its residents, family members, and team members among its highest priorities. Employment with Sunrise is contingent upon completing and passing a drug test (which does not include marijuana) and Tuberculosis Test, and a physical evaluation and a background check where required. Covid-19 and Influenza vaccination may be required if mandated by applicable federal, state, and local laws and authorities. COMPENSATION DISCLAIMER Selected candidates will be offered competitive compensation based on geographic [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
Construction Manager III (Solar and BESS/ Renewables-Nationwide Opportunities)
Overview Are you a proven leader in construction management with a passion for renewable energy? Join our team as a Construction
Manager and take charge of delivering safe, successful, [...]
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[...] and profitable utilityscale solar or battery energy storage projects across the country. This is your opportunity to lead from the fronton the sitewhere your decisions drive progress, safety, and sustainability. We hire Construction Managers III to oversee the full scope of utilityscale solar project sites, providing leadership across all key disciplines civil, mechanical, electrical, piles, and logistics. In this role, youll be responsible for managing the entire construction site operation, ensuring seamless integration of all workstreams to deliver [. .. ] Plan (ESPP) Flexible spending account (Healthcare Dependent care) Health Wellness Medical, Dental, and Vision insurance (plan choice) - coverage for spouse, domestic partner, and children Diabetes Management, Telehealth Coverage, Prescription Drug Plan, Pet Insurance, Weight Management Drug Discount Discounted National Gym Membership Network Family Lifestyle Paid Time Off, Paid Holidays, Bereavement Leave Military Leave, including Differential Pay and Benefits Continuation Employee Assistance Program Planning for the Unexpected Short and longterm disability, life insurance, and accidental death dismemberment Voluntary life insurance, accident, [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
Junior Computational Scientist-Translational Microbiome Research (f/m/d)
• München, Bayern
Absolventen, Einsteiger, Trainees
Jobticket
[. .. ] bacterial product (LBP) development. We are looking for a Junior Computational Scientist to join our Research team in Munich. The role sits at the intersection of computational [...]
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[...] biology and translational drug development, and is ideal for an earlycareer scientist with a Ph D and handson experience in biological or clinical data analysis. JOB DESCRIPTION Translational Analysis Analyze metagenomic, transcriptomic, metabolomic, and clinical biomarker data from ongoing clinical trials to support product development. Generate computational evidence for go/ nogo decisions at key development milestones (e. g. , donor selection, formulation optimization, safety signal evaluation) . Integrate multiomics datasets from patient cohorts to identify treatmentresponse biomarkers and inform clinical development strategy. Pipeline Development Computational R D Develop, validate, and maintain reproducible bioinformatics pipelines for strainlevel analysis, functional annotation, and community profiling. Contribute to the development of novel analytical approaches when offtheshelf tools are [. .. ] Eagerness to learn about drug development, regulatory requirements, and translational science. PREFERRED SKILLS/ ABILITIES Experience with microbial community analysis (compositional data, strainlevel methods, functional annotation) . Familiarity with a workflow manager (e. g. , Nextflow, Snakemake) or cloud computing platforms (GCP, AWS) . Exposure to clinical or regulated environments (e. g. , clinical trial data, IND preparation, Gx Padjacent work) . Experience with immunological or hostresponse datasets (flow cytometry, organoids, host transcriptomics) . Prior industry experience or internship in biotech/ pharma. [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
NPI Manager
• Stuttgart, Baden- Württemberg
[. .. ] climate-control solutions. Lennox is a global community that values each team members contributions and offers a supportive environment for career development. Come, stay, and grow with us. [...]
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[...] The NPI Manager is responsible for leading, developing, and optimizing manufacturing processes to ensure product quality, efficiency, and cost-effectiveness. This role oversees a team of engineers and technical staff, driving continuous improvement initiatives while aligning production capabilities with business objectives. The ideal candidate is a hands-on leader who can balance strategic [. .. ] coach, and develop a team of manufacturing engineers, technicians, and support staff Plan, prioritize, and assign projects based on team strengths and business needs Drive manufacturing engineering initiatives to meet safety, quality, delivery, and cost goals Collaborate with cross-functional teams to ensure alignment across engineering and production Review product designs for manufacturability and recommend improvements for quality and efficiency Lead cost reduction efforts across assembly processes and plant operations Ensure projects are executed on time and within budget Promote a [. .. ] this role are not eligible for overtime. Benefits : Subject to applicable eligibility requirements, the following benefits are offered for this role: tuition reimbursement; medical, dental, and vision insurance; prescription drug coverage; 401 (k) retirement plan; short-term disability insurance; 8 weeks paid birthing leave; 2 weeks paid bonding leave; life and long-term disability insurance. Depending on date of hire, and subject to applicable eligibility requirements, new employees in this role also receive up to: 12 days paid time off, [. .. ]
Job am 16.04.2026 bei Jobleads gefunden
Project Engineer I Solar
• Stuttgart, Baden- Württemberg
Sabbaticals
[. .. ] The Project Engineer will develop and maintain relationships with key stakeholders and support Construction Managers and Project Managers in delivering high-quality projects for our clients. Reporting to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Construction Manager or the Project Manager, the Project Engineer will collaborate with the Field Operations Team at site to ensure the successful execution of projects from initiation to substantial completion. The Project Engineer will lead the interface with Engineering, perform technical documentation reviews, manage RFIs, and ensure accurate construction drawings. They will [. .. ] part of the Site Management team and supports the overall planning and monitoring of works at site as well as client interface at site as required. Responsibilities HSQE: participates in safety meetings, safety walks, quality walks, reviews HSE compliance data, and supports continuous improvement. Ensures documentation is up-to-date in Procore and supports NCRs with the Site Quality Team. Maintains training and certifications for field staff. Client Relationship Management: manages and delivers projects in line with client expectations; coordinates between [. .. ] from occasional lifting and carrying to frequent standing and constant reading, grasping, hearing, vision, and repetitive motions. Exposure to extreme conditions and hazards may occur. Pre-employment background check and drug test required. RES is an equal opportunity employer committed to diversity and inclusion. #J-18808-Ljbffr 88799200 [. .. ]
Job am 07.04.2026 bei Jobleads gefunden
Senior Construction Electrical Project Manager I-Solar
Mortenson is currently seeking an experienced Senior Electrical
Manager to join our Solar group who is passionate about driving electrical design excellence and leading electrical
safety initiatives. In [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] this role you will shape project success across a regional portfolio by providing technical leadership, knowledge, and expertise throughout the entire process, from design to estimation, procurement, and completion of construction projects. We are looking for someone who will manage a portfolio of projects with a handson approachleading [. .. ] of contract fundamentals Active listening skills and effective communication Ability to travel up to 50 Knowledge of Equal Employment Opportunity, inclusive behaviors, and affirmative action plans Benefits Medical and prescription drug plans that includes no additional cost vision coverage Dental plan 401k retirement plan with a generous Mortenson match Paid time off, holidays, and other paid leaves Employer paid Life, AD D, and disability insurance Nocost mental health tool and concierge with extensive worklife resources Tuition reimbursement Adoption assistance Gym membership [. .. ]
Job am 05.04.2026 bei Jobleads gefunden
Clinical Research-Head of Gastroenterology II (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] integrity of clinical trials within this therapeutic area. GL collaborates with Clinical Research teams from other therapeutic areas and serves as a key liaison between Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gastroenterology II, Global Safety, Preand Early Clinical Research, and Regulatory and Medical Affairs. GL drives execution for assigned projects in collaboration with other crossfunctional stakeholders. Key Responsibilities Line manager for the organization/ project management of clinical studies in the Gastro II department Transfer of project responsibilities to assigned employees Review and approval of critical development documents (e. g. , Clinical Trial Protocol, master ICF, Statistical Analysis Plan, Clinical Trial Protocol) Review and negotiation of study budgets with service providers [. .. ] updates, phase transitions) Participation in reviewing the clinical sections of regulatory submission dossiers, documents for scientific consultations (e. g. , Scientific Advice, PIP, benefit dossier, etc. ) , or orphan drug applications in consultation with the Head of Clinical Research Participation in coordinating and drafting responses to clinical deficiency letters in regulatory procedures in consultation with the Head of Clinical Research Participation in the creation and revision of SOPs in the field of Clinical Research Attendance at national and international congresses [. .. ]
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Wieviel verdient man als Drug Safety Manager pro Jahr?
Als Drug Safety Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
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Aktuell gibt es auf JobRobot 35 offene Stellenanzeigen für Drug Safety Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Manager Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Drug Safety Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Drug Safety Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Safety Manager Stellenangebote:
- Veeva Systems (2 Jobs)
- HARMAN International (1 Job)
- IQVIA (1 Job)
- JSAN (1 Job)
- Allergopharma GmbH Co. KG (1 Job)
In welchen Bundesländern werden die meisten Drug Safety Manager Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Manager Jobs werden derzeit in Baden-Württemberg (7 Jobs), Bayern (6 Jobs) und Berlin (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Manager Jobs?
Drug Safety Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
