79 Jobs für Clinical Safety Associate
Stellenangebote Clinical Safety Associate Jobs
Job am 02.12.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
Associate Medical Director/ Medical Director About Us The development of novel, effective and safe therapies for the treatment of cancer is one of the main challenges for modern medicine. We [...]
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[...] want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of [. .. ] that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full lifecycle 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, [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
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[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle 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, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle 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, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Essen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle 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, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle 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, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Dortmund, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle 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, [. .. ]
Job am 13.09.2025 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] to advance our mission of transforming science into medicines for patients with disorders of the nervous system. The Opportunity In this role, you will lead and/or support [...]
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[...] early-stage clinical projects from entry into a human through proof of mechanism and proof of concept, to transform molecules into new medicines in an area with huge unmet medical needs. You will leverage your expertise to translate innovative molecules into potentially transformative therapies for patients with severe brain disorders. By marrying science [. .. ] development plans from Phase 1 through Phase 2 (proof-of-concept) Coach Clinical Scientists in a line-or functional-manager status Closely 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 [. .. ] has access to healthcare today and for generations to come. Our efforts result in millions treated with our medicines and billions of tests conducted with our Diagnostics products. Seniority level Associate Employment type Full-time Job function Research, Science, and Engineering Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing #J-18808-Ljbffr 61867989 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Director of Biological Data Science m/w/d
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] and combinations for therapeutic consortia. Data Integration and Analysis: Oversee the development and deployment of robust, reproducible computational pipelines for integrating and analyzing largescale multiomics datasets from [...]
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[...] preclinical models and clinical studies. Predictive Modeling: Apply advanced statistical and machine learning techniques to model microbiomehost interactions, predict LBP efficacy, and assess potential safety profiles. Cross Functional Collaboration: Partner with research, process development, and clinical teams to translate computational predictions into experimental designs and advance product candidates through the pipeline. External Engagement: Identify and manage strategic relationships with external collaborators, vendors, and academic institutions to augment internal capabilities. Subject Matter Expert: Act as a [. .. ] to articulate complex computational concepts to diverse scientific and business audiences and collaborate effectively with scientists and technical staff. Language: German language skills are a plus. Additional information Seniority level: Associate Employment type: Fulltime Job function: Project Management Industry: Pharmaceutical Manufacturing #J-18808-Ljbffr 72806154 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Berlin
Senior Research Fellow Dermatology, Randwick
Clinical Campus (UNSW) Employment Type: Full Time, 35 hours per week Duration: 12 months fixed term Remuneration: 150 K-172 K (based on experience) + [...]
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[...] 17 superannuation + leave loading Location: Randwick, New South Wales Why This Role Matters The Senior Research Fellow role involves conducting independent, high-impact research, building [. .. ] should have an expertise in cutaneous toxicities of immunotherapy. Strong leadership, collaboration, and organisational skills are essential, along with a commitment to professional development, ethical conduct, and workplace health and safety. The position will report to the Associate Professor and has no direct reports. Skills Required A Ph D in epidemiology, and/or relevant work experience with medical qualification and specialist qualification in dermatology (FACD or international equivalent) Experience in management of cutaneous toxicities of immunotherapy. Proven commitment to proactively keeping up to date with discipline knowledge and developments. [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Research Associate
• Hamburg
Veeda Lifesciences is seeking a
Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview [...]
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[...] The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] timelines with the Investigators Checks the storage and adequacy of clinical trial supplies Maintains and updates the Investigators Files as required to confirm completeness Co-ordinates the proper reporting of Safety Information to the Sponsor according to the Safety Reporting Plan, where applicable. CRA is also responsible for making sure that the Investigators are adequately trained in identifying and reporting AEs/ SAEs Checks that all submissions, reports, notifications and applications to the IEC/ IRB or Regulatory Authorities have been made by [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Dortmund, Nordrhein- Westfalen
Veeda Lifesciences is seeking a
Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] timelines with the Investigators Checks the storage and adequacy of clinical trial supplies Maintains and updates the Investigators Files as required to confirm completeness Co-ordinates the proper reporting of Safety Information to the Sponsor according to the Safety Reporting Plan, where applicable. CRA is also responsible for making sure that the Investigators are adequately trained in identifying and reporting AEs/ SAEs Checks that all submissions, reports, notifications and applications to the IEC/ IRB or Regulatory Authorities have been made by [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Research Associate
• Leipzig, Sachsen
Veeda Lifesciences is seeking a
Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] timelines with the Investigators Checks the storage and adequacy of clinical trial supplies Maintains and updates the Investigators Files as required to confirm completeness Co-ordinates the proper reporting of Safety Information to the Sponsor according to the Safety Reporting Plan, where applicable. CRA is also responsible for making sure that the Investigators are adequately trained in identifying and reporting AEs/ SAEs Checks that all submissions, reports, notifications and applications to the IEC/ IRB or Regulatory Authorities have been made by [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Senior/ Principal Research
Associate, Biochemical Methods in Neurodegeneration Drug Discovery (Basel) page is loaded # # Senior/ Principal Research Associate, Biochemical Methods in Neurodegeneration Drug Discovery (Basel) locations: Baseltime [...]
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[...] type: Full timeposted on: Posted Todaytime left to apply: End Date: December 25, 2025 (14 days left to apply) job requisition id: 202512-131752At Roche [. .. ] within at the heart of the NRD therapeutic area. The overarching goal of the Neural Signalling Section is to advance move forward drug discovery projects from target assessment to early clinical development phase. Our focus is in the therapeutic area of neurodegenerative diseases such as Alzheimers disease and Parkinsons disease. You will collaborate closely with experts across various laboratories within NRD, as well as with teams from other departments in the collaborative drug discovery matrix of p RED, to translate research hypotheses [. .. ] Laboratory Practice: As a teamplayer you contribute to the success and optimization of a highly collaborative sharing and caring laboratory work place. You maintain the highest level of diligence and safety in a BSL2 lab environment. Communication: You communicate, write, and present fluently in English and can discuss your work in front of small teams and larger groups. Apply now and upload your CV, letters of recommendation and degree certificates to get started. Please note, applicants with a Ph D cannot be [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Senior/ Principal Research Associate, Biochemical Methods in Neurodegeneration Drug Discovery (Basel)
• Basel, Basel- Stadt
[. .. ] cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position The Opportunity As a [...]
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[...] Biology Laboratory Research Associate, you will be an integral member and contributor within the Neural Signalling Section, a dynamic research unit within at the heart of the NRD therapeutic area. The overarching goal of the Neural Signalling Section is to advance move forward drug discovery projects from target assessment to early clinical development phase. Our focus is in the therapeutic area of neurodegenerative diseases such as Alzheimers disease and Parkinsons disease. You will collaborate closely with experts across various laboratories within NRD, as well as with teams from other departments in the collaborative drug discovery matrix of p RED, to translate research hypotheses [. .. ] Laboratory Practice: As a teamplayer you contribute to the success and optimization of a highly collaborative sharing and caring laboratory work place. You maintain the highest level of diligence and safety in a BSL2 lab environment. Communication: You communicate, write, and present fluently in English and can discuss your work in front of small teams and larger groups. Ready to take the next step in your career? Were excited to see what youll bring to the team. Apply now and upload [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] job and more exclusive features. Description CRA Germany or Austria-single-client Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate [...]
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[...] unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work [. .. ] 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 [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Clinical Research Associate
• Düsseldorf, Nordrhein- Westfalen
Veeda Lifesciences is seeking a
Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] timelines with the Investigators Checks the storage and adequacy of clinical trial supplies Maintains and updates the Investigators Files as required to confirm completeness Co-ordinates the proper reporting of Safety Information to the Sponsor according to the Safety Reporting Plan, where applicable. CRA is also responsible for making sure that the Investigators are adequately trained in identifying and reporting AEs/ SAEs Checks that all submissions, reports, notifications and applications to the IEC/ IRB or Regulatory Authorities have been made by [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Senior Research Fellow-Dermatology, Randwick Clinical Campus
• Zürich
[. .. ] should have an expertise in cutaneous toxicities of immunotherapy. Strong leadership, collaboration, and organisational skills are essential, along with a commitment to professional development, ethical conduct, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] workplace health and safety. The position will report to the Associate Professor and has no direct reports. Skills Required A Ph D in epidemiology, and/or relevant work experience with medical qualification and specialist qualification in dermatology (FACD or international equivalent) Experience in management of cutaneous toxicities of immunotherapy. Proven commitment to proactively keeping up to date with discipline knowledge and developments. [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Clinical Research Associate Sponsor Dedicated in Austria
• Wien
Clinical Research
Associate Sponsor Dedicated in Austria Join to apply for the Clinical Research Associate Sponsor Dedicated in Austria role at Fortrea Principal Talent Acquisition Partner DACH at [...]
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[...] Fortrea/ Driving Data-Driven Talent Strategies/ Stakeholder Engagement/ DEI Advocate We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager [. .. ] Key Responsibilities Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements Build strong relationships with investigators and site staff Ensure high-quality data collection and patient safety Work closely with the sponsor, providing insights and updates on study progress Perform on-site monitoring visits Qualifications University or college degree, or certification in a related allied health profession from an appropriately accredited institution (Fortrea may consider relevant and equivalent experience in lieu of educational requirements) Thorough understanding of [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Associate Director, Distribution Quality Join to apply for the Associate Director, Distribution Quality role at Be One Medicines Be One continues to grow at a rapid pace with challenging [...]
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[...] and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and [. .. ] GSP requirements and other regulatory requirements and industry best practices. Monitor trends of GDP regulations and guidelines, integrating GDP requirements into Be One processes and systems. Engage with commercial and clinical teams to ensure quality is built into long term planning and that the proposed supply chain distribution models are compliant with current and future GDP/ GSP requirements and expectations. Improve GDP/ GSP knowledge and understanding throughout Be One. Support fostering a culture of continuous improvement and excellence in quality management, [. .. ] processes are in place and demonstrating a state of control. Monitor key performance metrics of distribution processes to ensure that distribution activities comply with GDP/ GSP requirements, maintaining the quality, safety and efficacy of pharmaceutical products throughout the supply chain. Cultivate productive and collaborative relationships across functional areas and geographies, including Commercial, Pharmacovigilance, Medical, Supply Chain, Operations, Internal and External Supply Quality, Regulatory Affairs and Regional Quality teams. Supervisory Responsibilities None Computer Skills PC literate with MS Office skills (Project Plan, [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
HTE Principal Associate/ Scientist in Process Chemistry Catalysis (2 year fixed term contract)
• Basel, Basel- Stadt
[. .. ] necessary support for regulatory submissions. We are a key part of Small Molecules Technical Development (PTDC) , which develops our synthetic pipeline and manufactures drug substance and [...]
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[...] drug product for clinical studies, collaborating closely with research partners and the commercial manufacturing network. We are seeking a highly motivated and technically skilled early career scientist to join the PTDC-C team. This is a handson laboratory role situated at the nexus of modern chemistry, automation, and data science, where you will be [. .. ] by evaluating new technologies, identifying bottlenecks, and optimizing protocols for efficiency, robustness, and data quality. Support the training and supervision of junior associates or interns, actively promoting a culture of safety, precision, and collaboration. Ensure all work is meticulously documented, analyzed, and presented to project teams. Who You Are Hold a Degree in Chemistry or Chemical Engineering and possess a minimum of 2 years (with Masters) or 4 years (with Bachelors) of relevant industrial or academic experience, preferably in process chemistry, [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Associate Director of Medical Operations
Führungs-/ Leitungspositionen
Job Title:
Associate Director of Medical Operations (ADMO) Location: Multi-site (Regional) Reports To: Director of Medical Operations Position Summary The Associate Director of Medical Operations (ADMO) is a strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and operational leadership role responsible for the medical quality, performance, development, and engagement of the DVM teams across a portfolio of hospitals. The [. .. ] based medicine while aligning medical initiatives with organizational goals. The ADMO serves as a coach, mentor, and resource for hospital-level MDs and is instrumental in driving a culture of clinical excellence, patient safety, and team wellbeing. Medical Initiatives Provides feedback and coaching to Medical Directors to provide the highest level of care for clients and patients. Responsible for overseeing the development and maintenance of medical policies and medical SOPs for the hospitals. Provides feedback and coaching to Medical Directors and DVMs to ensure [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior Research Fellow-Dermatology, Randwick Clinical Campus
• Frankfurt, Hesse
Senior Research Fellow (National Centre for
Clinical Research on Emerging Drugs) Location: Randwick, New South Wales, Australia Employment Type: Full Time, 35 hours per week Duration: 12 months fixed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] term Remuneration: 150 K-172 K (based on experience) + 17 superannuation + leave loading Why This Role Matters The Senior Research Fellow role involves conducting independent, highimpact [. .. ] Candidates should have expertise in cutaneous toxicities of immunotherapy. Strong leadership, collaboration and organisational skills are essential, along with a commitment to professional development, ethical conduct and workplace health and safety. The position will report to the Associate Professor and has no direct reports. Key Responsibilities Conduct independent, highimpact research in cutaneous toxicities of immunotherapy. Secure competitive research funding and establish national research networks. Mentor students and colleagues. Skills Required A Ph D in epidemiology, and/or relevant work experience with medical qualification and specialist qualification in dermatology (FACD [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
HTE Principal Associate/ Scientist in Process Chemistry Catalysis
• Basel, Basel- Stadt
HTE Principal
Associate/ Scientist in Process Chemistry Catalysis page is loaded # # HTE Principal Associate/ Scientist in Process Chemistry Catalysislocations: Baseltime type: Full timeposted on: Posted Todayjob requisition [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] id: 202511-129598At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, [. .. ] necessary support for regulatory submissions. We are a key part of Small Molecules Technical Development (PTDC) , which develops our synthetic pipeline and manufactures drug substance and drug product for clinical studies, collaborating closely with research partners and the commercial manufacturing network. We are seeking a highly motivated and technically skilled early career scientist to join the PTDC-C team. This is a hands-on laboratory role situated at the nexus of modern chemistry, automation, and data science, where you will [. .. ] by evaluating new technologies, identifying bottlenecks, and optimizing protocols for efficiency, robustness, and data quality. Support the training and supervision of junior associates or interns, actively promoting a culture of safety, precision, and collaboration. Ensure all work is meticulously documented, analyzed, and presented to project teams. # # # Who You Are Hold a Degree in Chemistry or Chemical Engineering and possess a minimum of 2 years (with Masters) or 4 years (with Bachelors) of relevant industrial or academic experience, [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
Manager/
Associate Principal, EMEA Strategy Supply Operations Consulting Location: Munich or Basel Solution Area: Operations Consulting, Life Sciences Real World Commercial Solutions to Create a Healthier World In RWCS [...]
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[...] were passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. Were purposedriven problem [. .. ] in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments, costbenefit analyses of local vs. offshore manufacturing, and develop risk mitigation plans (dual sourcing, safety stock, etc. ) . Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs (e. g. optimizing warehouse locations or delivery routes) . Propose solutions like route optimization, 3PL partner changes, or technology enhancements. Advanced Therapy Supply Planning: Work on [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Manager/
Associate Principal, EMEA Strategy Supply Operations Consulting Location: Munich or Basel Solution Area: Operations Consulting, Life Sciences Real World Commercial Solutions to Create a Healthier World In RWCS [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] were passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. Were purposedriven problem [. .. ] in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments, costbenefit analyses of local vs. offshore manufacturing, and develop risk mitigation plans (dual sourcing, safety stock, etc. ) . Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs (e. g. optimizing warehouse locations or delivery routes) . Propose solutions like route optimization, 3PL partner changes, or technology enhancements. Advanced Therapy Supply Planning: Work on [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical safety associate pro Jahr?
Als Clinical safety associate verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Safety Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 79 offene Stellenanzeigen für Clinical Safety Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Safety Associate Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Safety Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Safety Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Safety Associate Stellenangebote:
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- ICON (4 Jobs)
- IQVIA (3 Jobs)
- Herman Medical Staffing GmbH (1 Job)
In welchen Bundesländern werden die meisten Clinical Safety Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Safety Associate Jobs werden derzeit in Nordrhein-Westfalen (13 Jobs), Berlin (8 Jobs) und Niedersachsen (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Safety Associate Jobs?
Clinical Safety Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
