Clinical Safety Associate Stellenangebote


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Stellenangebote Clinical Safety Associate Jobs


Job vor 3 Tagen bei Jobleads gefunden

Associate Medical Director/ Medical Director

• Frankfurt (Oder) , Brandenburg 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 cross-functional team involved with site evaluation, study [. .. ]

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Job am 02.12.2025 bei Jobleads gefunden Associate Medical Director/ Medical Director 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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, [. .. ]

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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 [...]
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, [. .. ]

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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, [. .. ]

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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, [. .. ]

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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, [. .. ]

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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, [. .. ]

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Job am 04.10.2025 bei Jobleads gefunden Associate Medical Director/ Medical Director • Leipzig, Sachsen Führungs-/ Leitungspositionen [. .. ] of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Your [...]
MEHR INFOS ZUM STELLENANGEBOT[...] mission Provide clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program. Lead development of clinical sections of trial and program level regulatory documents such as protocol amendments, imaging/ pathology/ DSMB charters, briefing books, BLA/ MAA, ODD, breakthrough applications etc. Act as clinical [. .. ] 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 [. .. ]

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Job am 13.09.2025 bei Jobleads gefunden

Medical Director Multiple Sclerosis

• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job am 11.07.2025 bei Jobleads gefunden Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, German. . . • Baden- Württemberg Führungs-/ Leitungspositionen Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, Germany, or relocation to Germany (relocation assistance available) . #clientvacancy #director #pv oncology Together with a German member of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] INRALS (International Network of Recruitment Agencies in Life Sciences) , we are looking for an Associate Director Patient Safety Physician (gn) for [. .. ] the global initiatives for Patient Safety and Pharmacovigilance (PSPV) and Risk Management (RM) pertaining to compounds at various stages of development. In this role, you will work closely with the clinical development department and will be involved in a very strategic and global function. TASKS RESPONSIBILITIES: Crafting proactive, patient-centric RM strategies tailored to designated compounds. Overseeing and executing all PV activities pertinent to assigned drugs, encompassing database setup, continual safety monitoring, and addressing safety concerns. Engaging in cross-functional collaboration [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

Clinical Research Associate-FSP-Remote

Clinical Research Associate-FSP-Remote Join to apply for the Clinical Research Associate-FSP-Remote role at ICON Strategic Solutions. ICON plc is a worldleading healthcare intelligence and clinical research organization. Were [...]
MEHR INFOS ZUM STELLENANGEBOT[...] proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to [. .. ] the advancement of innovative treatments and therapies. What You Will Be Doing Conducting site qualification, initiation, monitoring, and closeout visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain highquality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelors degree in a scientific or [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden Clinical Research Associate-Sponsor dedicated • Frankfurt, Hesse Work-Life-Balance Overview CRA, Germany, sponsor dedicated ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we [...]
MEHR INFOS ZUM STELLENANGEBOT[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelors degree in a scientific [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden Clinical Research Associate-FSP-Remote • Frankfurt (Oder) , Brandenburg Clinical Research Associate-FSP-Remote ICON plc is a worldleading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome [...]
MEHR INFOS ZUM STELLENANGEBOT[...] you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II [. .. ] the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and closeout visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain highquality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelors degree in a scientific or [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden Medical Affairs Lead (m/f/d) • Hamburg Führungs-/ Leitungspositionen Join to apply for the Medical Affairs Lead (m/f/d) role at seca precision for health. We firmly believe that the safety and well-being of patients are the highest values [...]
MEHR INFOS ZUM STELLENANGEBOT[...] when it comes to healthcare. Ensuring these begins with the smallest details every gram, every millimeter, every decimal point, and every single heartbeat. When it comes to medical evaluations and decisions, there is no such thing as approximately or roughly. Thats [. .. ] someone who shares our values and standards and is committed to maintaining our position as a global market leader. In this role, you will lead medical strategy and execution across clinical development, evidence generation, and scientific communication. By connecting clinical expertise with innovation and commercial goals, youll support product development, market positioning, and stakeholder engagement. You will shape our medical roadmap, build strong KOL relationships, and ensure our scientific efforts align with longterm objectives. Your Responsibilities KOL Engagement: Build and nurture [. .. ] date as well as your salary expectation, through our online application form. Referrals increase your chances of interviewing at seca precision for health by 2x. Job Details Seniority level : Associate Employment type : Fulltime Job function : Product Management, Business Development, and Science Industries : Software Development and Medical Equipment Manufacturing #J-18808-Ljbffr 73265174 [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden

P C Business Partner

• Basel, Basel- Stadt [. .. ] of millions. We maximize impact for patients with cancer by translating biological insights into meaningful therapies. Pharmaceutical Sciences (PS) provides the evidence that a molecule is safe [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and efficacious in clinical proof of concept studies and can be filed as a new medicine. The position leads and drives change initiatives, people streams, Work Product Teams (WPTs) , and squads to embed and execute P C strategies effectively. Additionally, it may contribute to WPTs, squads, or initiatives in other areas of the [. .. ] You exhibit a creative mindset, high selfawareness, and act as a coach and mentor for other leaders. Building a culture of inclusion and belonging is a top priority, fostering psychological safety and a sense of belonging. You recognise the impact each employee has on Roches purpose and ambitions. You have already excelled as a P C Business Partner in navigating the P C system, collaborating with global teams, and forming teams to deliver on business and P C strategies. You diagnose [. .. ] explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver lifechanging healthcare solutions that make a global impact. Lets build a healthier future, together. Seniority level Associate Employment type Fulltime Job function Human Resources Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing Roche is an Equal Opportunity Employer. Get notified about new Business Partner jobs in Basel, Basel, Switzerland. #J-18808-Ljbffr 73212083 [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden Associate Director, Technical Operations • Couvet, Neuenburg Führungs-/ Leitungspositionen Associate Director, Technical Operations Wu Xi App Tec is a trusted partner and contributor to the pharmaceutical and life sciences industries, providing R D and manufacturing services that help [...]
MEHR INFOS ZUM STELLENANGEBOT[...] advance healthcare innovation. With operations across Asia, Europe, and North America, we offer integrated, endtoend services through our unique CRDMO (Contract Research, [. .. ] will use your strong OSD Drug Product technical skills to ensure the successful transfer of Drug Products to the Couvet site, Switzerland. This includes the ontimeinfull supply of technical, registration, clinical, stability, and PPQ batches. The position reports to the Vice President, Head of Late Stage Formulation R D and Commercialization, and Head of Business Development for China. Responsibilities Accountable for the ontime start of bulk manufacturing and packaging batches. Accountable for the ontime delivery of registration, clinical and stability batches. [. .. ] and troubleshooting of production. Author technical working instructions (including batch records) of various manufacturing technologies to ensure the production operation is compliant with the GMP policy and satisfies the highest safety standard. Support deviations by leveraging technical expertise, manufacturing experience, and investigative skills. Provide technical training and seminars to personnel of other departments to promote the application of new manufacturing technologies and resolve misconceptions and miscommunication. Accountable for process validation (PPQ) , including continued process verification. Accountable for cleaning validation, including [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden

Associate Director/ Director CMC Product Development (all genders) (fulltime, permanent)

Führungs-/ Leitungspositionen Work-Life-Balance [. .. ] product. You serve as the spokesperson for all CMC functions and ensures information flow among AST and various line functions and stakeholders. You will also partner with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] key collaborators, incl. Clinical, Regulatory, Operations, Quality, Preclinical Safety, ADME and Commercial organizations. Apprises CMC and Stakeholder Management of strategies, plans and risks through regular communications and periodic reviews throughout development and in support of global filings and approvals. In addition you support and implement CMC functional initiatives and across-asset strategies. Make your mark by: Representingall CMC areas [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden Senior/ Principal Research Associate, Biochemical Methods in Neurodegeneration Drug Discovery (Basel) • Penzberg, Bayern [. .. ] Position At Roche, we believe it is urgent to deliver medical solutions right now, and we are passionate about transforming patients lives. We are looking for a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] highly motivated Research Associate to join our team within the Research Department of the Neuroscience and Rare Diseases (NRD) Therapeutic Area in Pharma Research and Early Development (p RED) . In this role you will help to advance our understanding of neurodegenerative disease pathology and translate research hypotheses into innovative therapeutics. The Opportunity As a [. .. ] within the Neural Signalling Section, a dynamic research unit within NRD therapeutic. The goal of the Neural Signalling Section is to advance drug discovery projects from target assessment to early clinical development. Our focus are 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 into innovative therapeutics that address brain [. .. ] 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 [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden

Sponsor-Focused Clinical Research Associate-Remote/ Hybrid

• Wien A clinical research organization in Austria is seeking a Clinical Research Associate to monitor clinical trial sites and ensure compliance with protocols and safety regulations. The ideal [...]
MEHR INFOS ZUM STELLENANGEBOT[...] candidate will possess a university degree in a related field and be fluent in both German and English. This role offers a competitive salary, performance bonuses, and flexible work arrangements. If youre ready to advance your CRA career, apply now #J-18808-Ljbffr 73154327 [. .. ]

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Job vor 8 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 8 Tagen bei Jobleads gefunden Senior Research Fellow-Dermatology, Randwick Clinical Campus • 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) + [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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. [. .. ]

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Job vor 12 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden Senior/ Principal Research Associate, Biochemical Methods in Neurodegeneration Drug Discovery (Basel) • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden CRA Germany or Austria-single-client • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 13 Tagen bei Jobleads gefunden Associate Director, Biostatistics-Global BIOS • Frankfurt, Hesse Führungs-/ Leitungspositionen Work-Life-Balance Associate Director, Biostatistics-Permanent-w/m/d Global Biostatistics Home-Based/Hybrid: Germany Join us on our exciting journey The Global Biostatistics (Data Sciences, Safety Medical) team at IQVIA are experienced in submissions for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability. We have one of the largest Biostatistics departments within the industry of around 1, 100+ [. .. ] have the opportunity to work globally and across a variety of therapeutic areas. IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting. Job Overview As an Associate Director, Biostatistics, with regional/ site presence, you will manage a team of Biostatistics staff and fulfil the role of site head or functional head within a site. You will provide direction and guidance in [. .. ]

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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 93 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 (5 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 (12 Jobs), Bayern (9 Jobs) und Niedersachsen (9 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Safety Associate Jobs?

Clinical Safety Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.


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Dauer: 0.0557 s., Vers. V.2025-d-2009-Ind-141