Clinical Safety Associate Stellenangebote


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Stellenangebote Clinical Safety Associate Jobs


Job vor 2 Tagen bei Mindmatch.ai gefunden ICON

Clinical Research Associate (CRA) - Austria

• AT- 9 Wien Work-Life-Balance CRA. Austria 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 welcome you to join [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 Mindmatch.ai gefunden ICON Strategic Solutions Clinical Research Associate • AT- 8 Gemeinde Au CRA II, Home-based in Sydney or Melbourne Join a global FSP partnership ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment [...]
MEHR INFOS ZUM STELLENANGEBOT[...] driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As an experienced Clinical Research Associate, you will be joining the worlds largest most comprehensive clinical research organization, powered by healthcare intelligence. You will be working alongside a world-leading pharmaceutical company. This 22year partnership is focused on leveraging cuttingedge science to make a positive impact in the therapeutic areas of cancer, cardiometabolic, vaccines, and oncology, [. .. ] could be the career destination for you. 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 4 Tagen bei Mindmatch.ai gefunden ICON Strategic Solutions

Senior CRA

• AT- 8 Gemeinde Au [. .. ] are interested in managing the whole life cycle of the study from site selection to closeout, we want to hear from you. ICON plc is a worldleading [...]
MEHR INFOS ZUM STELLENANGEBOT[...] healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking an experienced Clinical Research Associate II or Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials of a single client by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. In this FSP program you will be working on cuttingedge Oncology trials and can take ownership of the full site management lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) [. .. ]

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Job vor 6 Tagen bei Mindmatch.ai gefunden ICON Strategic Solutions Clinical Research Associate/ Senior CRA • AT- 8 Gemeinde Au Clinical Research Associate/ Senior Clinical Research Associate Sydney Home based ICON plc is a worldleading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking [. .. ] professional career while making a truly impact. 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 10 Tagen bei Mindmatch.ai gefunden allaboutvienna

Healthcare Medical

• AT- 9 Wien [. .. ] of Europe (CIRSE) is a non-profit making, educational and scientific association aiming to improve patient care through the support of. . . Permanent Austria-Wien 9 hours ago [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Patient Safety Lead (f/m/d) At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted. . . Permanent Iqvia Austria-Wien 9 hours ago Project Manager, Study Operations, Cronos Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an. . . Permanent Austria-Wien 9 hours ago Public Affairs Manager (f/m/d) Job Description Summary #LI-Hybrid Location: Vienna, Austria At Novartis, one of [. .. ] our unique strengths, we are redefining healthcare through sustainable action and innovation. For a behind-the-scenes look, check out this. . . Permanent Ifc Austria-Wien 9 hours ago (Associate) Investment Officer (Associate) Investment Officer Job #: req34988 Organization: IFC Sector: Operations Grade: GF Term Duration: 3 years 0 months Recruitment Type: Local Recruitment Location: Vienna, Austr. . . Permanent Austria-Wien 9 hours ago Human Factors Engineer Medical Apps UX Usability A leading global healthcare company in Vienna [. .. ]

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Job vor 14 Tagen bei Mindmatch.ai gefunden Medtronic plc Clinical Specialist Surgical Robotics (m/w/d) - DACH • AT- 9 Wien Clinical Specialist Surgical Robotics (m/w/d) - DACH page is loaded # # Clinical Specialist Surgical Robotics (m/w/d) - DAC Hremote type: Remotelocations: Vienna, Vienna, Austriatime type: Full timeposted on: [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Posted 6 Days Agojob requisition id: R49645At Medtronic you can begin a life-long career of exploration and [. .. ] daily healthcare delivery. The Surgical Robotics Utilization Team plays a key role in supporting the successful installation, start-up, and integration of the Hugo Surgical Robot in hospitals. As an Associate Start Up Specialist, you will work alongside experienced professionals to help ensure smooth adoption of this innovative technology by assisting with system setup, user training, and operational support. This role is designed for ambitious individuals looking to kick-start their careers in medical technology, healthcare operations, and surgical support. You [. .. ] proactive attitude in tackling challenges. Willingness to travel within the region (up to 75 travel) . Ability to work in a structured, detail-oriented way, with a focus on patient safety and efficiency. Driving license Yearly targeted salary starting from 45.000, 00 with the willingness to market-based overpayment depending on professional qualification and experience (Information only for Austria) . Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by [. .. ]

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Job am 17.11.2025 bei Mindmatch.ai gefunden Syneos Health

Experienced CRA Austria

• AT- 9 Wien Experienced CRA Austria Syneos Health Application open. Position sought for Experienced Clinical Research Associate in Austria. Description Syneos Health is a leading fully integrated biopharmaceutical solutions organization built [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of everything we [. .. ] to evaluate site performance and provide recommendations, communicate/ escalate serious issues, and develop action plans. Verify informed consent procedures are performed and documented for each subject, protecting confidentiality and assessing safety and data integrity at investigator sites. Based on the Clinical Monitoring/ Site Management Plan, assess site processes, conduct source document review, verify CRF data accuracy, resolve queries remotely or onsite, support data capture and electronic data capture compliance. Perform IP inventory, reconciliation, storage and security review, and confirm correct dispensing [. .. ]

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Job am 17.11.2025 bei Mindmatch.ai gefunden Roche Patient Safety Lead (f/m/d) • AT- 9 Wien Führungs-/ Leitungspositionen [. .. ] stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Drive the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] future of patient safety at Roche Austria: You will strategically lead the local Pharmacovigilance (PV) system, encompassing its full implementation, maintenance, and oversight. This role requires setting the strategic direction for patient safety and risk management, balancing global International Patient Safety standards with critical local business demands. Youll have the chance to drive impactful [. .. ] timely safety communication to healthcare professionals, patients, and external stakeholders, in partnership with Medical Affairs and the cross-functional team Who you are At least 3-5 years experience in clinical research, development, or related field; including a minimum of 3 years in PV or Safety 3+ years experience collaborating or leading in global and local matrix environments, including proven ability in stakeholder management and influencing Experience and expertise of relevant PV and medical device regulation, interaction with Health Authorities Degree [. .. ] year and attractive benefits. Flexible working hours, workplace health promotion and various sports programs, just to name a few. Depending on your qualifications and experience, overpayment is possible. Seniority level Associate Employment type Full-time Job function Research, Science, and Engineering Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing Referrals increase your chances of interviewing at Roche by 2x. Who we are A healthier future drives us to innovate. Together, more than 100, 000 employees across the globe are dedicated [. .. ]

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Job am 04.11.2025 bei Mindmatch.ai gefunden Medtronic

Clinical Specialist Surgical Robotics (m/w/d) - DACH

• AT- 9 Wien Clinical Specialist Surgical Robotics (m/w/d) - DACH Join to apply for the Clinical Specialist Surgical Robotics (m/w/d) - DACH role at Medtronic At Medtronic you can begin a lifelong [...]
MEHR INFOS ZUM STELLENANGEBOT[...] career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, [. .. ] in daily healthcare delivery. The Surgical Robotics Utilization Team plays a key role in supporting the successful installation, startup, and integration of the Hugo Surgical Robot in hospitals. As an Associate Start Up Specialist, you will work alongside experienced professionals to help ensure smooth adoption of this innovative technology by assisting with system setup, user training, and operational support. This role is designed for ambitious individuals looking to kickstart their careers in medical technology, healthcare operations, and surgical support. You will [. .. ] a proactive attitude in tackling challenges. Willingness to travel within the region (up to 75 travel) . Ability to work in a structured, detailoriented way, with a focus on patient safety and efficiency. Driving license. Yearly targeted salary starting from 45, 000.00, with potential marketbased adjustments depending on professional qualification and experience (information only for Austria) . Physical Job Requirements The above statements describe the general nature and level of work performed by employees assigned to this position, but they [. .. ]

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Job am 14.10.2025 bei Mindmatch.ai gefunden Syneos Health CRA Austria • AT- 9 Wien 2 days ago Be among the first 25 applicants Description CRA Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 4 Tagen 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. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] We 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 09.11.2025 bei Jobleads gefunden Associate Medical Director/ Medical Director • Hamburg 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 17.10.2025 bei Jobleads gefunden Associate Medical Director/ Medical Director • Stuttgart, Baden- Württemberg 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 • 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 • Frankfurt, Hesse 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 16.09.2025 bei Jobleads gefunden Associate Medical Director, Cardiology-Metabolic Diseases and Nephrology Experience (m/w/d) • Frankfurt, Hesse Führungs-/ Leitungspositionen Job Overview The Associate Medical Director/ Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions Medical Monitoring: Primarily serves as Global Medical Advisor on [. .. ] medical and scientific aspects of assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/ exclusion determinations, and issues of patient safety and/or eligibility. Performs medical review of the protocol, Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform [. .. ]

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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 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 [. .. ]

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Job gestern 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, [. .. ]

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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 93 offene Stellenanzeigen für Clinical Safety Associate Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Safety Associate Jobs?

Aktuell suchen 12 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:


  • Planet Pharma (11 Jobs)
  • Tubulis GmbH (11 Jobs)
  • ICON (3 Jobs)
  • ICON Strategic Solutions (3 Jobs)
  • IQVIA (3 Jobs)
  • Syneos Health (2 Jobs)


In welchen Bundesländern werden die meisten Clinical Safety Associate Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Safety Associate Jobs werden derzeit in Nordrhein-Westfalen (11 Jobs), Berlin (9 Jobs) und Bayern (6 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Safety Associate Jobs?

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


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