58 Jobs für Clinical Safety Associate
Stellenangebote Clinical Safety Associate Jobs
Job vor 5 Tagen bei Mindmatch.ai gefunden
ICON
• AT- 9 Wien
Work-Life-Balance
Senior CRA 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 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 by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
AOP Health
Clinical Site Management Lead (30h/ week up to full-time)
• AT- 9 Wien
Führungs-/ Leitungspositionen
We are looking for an experienced and proactive
Clinical Site Management Lead to oversee the operational management of clinical studies and ensure high standards of quality, compliance, and collaboration with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study sites and partners. What Your Day To Day Will Look Like Manage assigned clinical studies from site start-up through close-out Prepare and coordinate submissions to Competent Authorities and Ethics Committees Conduct co-monitoring visits to ensure patient safety, data integrity, and regulatory compliance Build strong relationships with CRO personnel, site staff, and internal study teams Support and oversee CROs and freelance CRAs Review and analyse clinical study data for accuracy and completeness Ensure availability and quality of essential site documents for the Trial Master File Forecast IMP supply [. .. ] smooth trial execution Your Qualifications And Experience Bachelors degree or higher in Life Sciences, Pharmacy, Medical Sciences, or a related field Minimum 5 years of experience as a Clinical Research Associate (CRA) or 2 years as a Senior CRA Strong knowledge of clinical trial conduct, regulatory requirements, and ICH-GCP Experience with submissions to Competent Authorities and Ethics Committees Experience with risk-based monitoring Willingness to travel (max. 30-irregular, but can be flexibly divided in the team) Fluent in English [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
ICON
• AT- 9 Wien
Work-Life-Balance
A leading healthcare organization in Austria is seeking an experienced Senior
Clinical Research
Associate to oversee clinical trial activities and ensure regulatory compliance. The ideal candidate will have an advanced [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] degree in a relevant field and extensive experience in clinical trial processes. You will monitor trial sites, conduct site visits, and collaborate with teams to ensure data integrity and participant safety. ICON offers a competitive salary and comprehensive benefits to support work-life balance. J-18808-Ljbffr 85227186 [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on our side-[. .. ] with SOPs, protocol, and GCP. Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Description CRA single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. For 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 [. .. ] oversight of the Lead CRA, to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA) . Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Octapharma Austria
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
• AT- 9 Wien
[. .. ] highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 4, 270.14 [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
Octapharma Pharmazeutika Produktionsges. m. b. H.
• AT- 9 Wien
[. .. ] highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 4, 270.14 [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA Germany or Austria-single-client
• AT- 9 Wien
[. .. ] 9, 2025 Location: Vienna, 1, Austria Job ID: 25104265-OTHLOC-3538-2DR 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 projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA single sponsor-Germany
• AT- 9 Wien
Updated: Yesterday Location: Vienna, 1, Austria Job ID: 25105750-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 projectspecific 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 to [. .. ]
Job am 22.02.2026 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 [. .. ]
Job am 10.03.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The Study Physician is a critical global role responsible for assuming medical oversight of
clinical trials within Clinical Development Operations. This position requires a qualified and clinically experienced physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] who will provide comprehensive medical expertise throughout all phases of the trialfrom preparation and conduct to reporting. The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to [. .. ] both the Trial Team and the Evidence Network Team. Study Physician services Medical Content Oversight: Responsible for medical content in Clinical Trial Protocols (CTPs) . Collaborates with Project Management, Patient Safety, Medical Writers, and trial/ evidence teams. Provides medical input for CTP updates. Risk-Based Quality Management: Defines medically critical data/ processes and associated risks. Contributes to Integrated Quality and Risk Management Plan (IQRMP) . Participates in risk discussions during trial conduct. Clinical Quality Monitoring: Co-authors Clinical Quality Monitoring Plan [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
Associate Medical Director-Oncology, Sponsor-Dedicated (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The Study Physician is a critical global role responsible for assuming medical oversight of
clinical trials within Clinical Development Operations. This position requires a qualified and clinically experienced physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] who will provide comprehensive medical expertise throughout all phases of the trialfrom preparation and conduct to reporting. The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to [. .. ] core member of both the Trial Team and the Evidence Network Team. Medical Content Oversight Responsible for medical content in Clinical Trial Protocols (CTPs) . Collaborates with Project Management, Patient Safety, Medical Writers, and trial/ evidence teams. Provides medical input for CTP updates. Risk-Based Quality Management Defines medically critical data/ processes and associated risks. Contributes to Integrated Quality and Risk Management Plan (IQRMP) . Participates in risk discussions during trial conduct. Clinical Quality Monitoring Co-authors Clinical Quality Monitoring Plan [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] Veeva. We work with senior customer stakeholders, as the partner of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Regulatory Affairs, Clinical Strategy Operations as well as Quality and Safety (eg. Pharmacovigilance) . As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R D planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through facetoface discussions, workshops, email, etc. ) to [. .. ] faced by the customer Be a primary client contact for operational project questions, developing the relationship through facetoface discussions, workshops, phone, and email contact Manage the work and priorities of Associate Consultants in your workstream Support and mentor Associates in developing skills and professional capabilities Build trusted relationships with customer stakeholders Bring to your customers a good level of industry/ market/ functional insights Input into business development opportunities and proposals Help develop and disseminate thought leadership Requirements Bachelors or Masters degree [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Support Associate, Germany (Remote/ Hybrid)
• Berlin
[. .. ] weight management programs combining GLP-1 medication with a tailored nutrition and exercise programme, supported by our multidisciplinary care team of prescribers, health coaches, dietitians, nurses and pharmacists. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Our published clinical research demonstrates that our combined approach to weight management and lifestyle change means that our patients are 4x as likely to lose significant weight through their course of treatment with Juniper. Since launching, weve grown fast to support millions of patients. In 2024 alone In the UK we grew from [. .. ] sustained health outcomes. Join us to be a critical part of our growth journey here in Germany What youll do (Responsibilities) : Triage medical enquiries efficiently to ensure excellent patient safety and care is received Provide outstanding medical advice to Juniper patients (by email and phone) Respond to patients experiencing side effects and/or symptoms related or unrelated to their medication Proactively engaging with patients throughout their treatment journey Create educational content to provide our patients with personalised and consistently high [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Planegg, Bayern
Führungs-/ Leitungspositionen
Associate Director Operational Excellence (m/f/d) Permanent employee, Full-time Planegg (Germany) , Remote (Germany) Be part of our team We are seeking a highly experienced Associate Director of Operational Excellence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (GCP) to lead continuous improvement efforts across our clinical trial operations and ensure adherence to the highest standards of GCP compliance. The position will be within the Quality Assurance (QA) department. We are a dedicated QA team supporting our development of antibody-drug conjugates (ADCs) and clinical trials with a strong focus on reliable processes and patient safety. Working closely together, we ensure that quality and compliance are part of every step, from research to clinical application. Our team values open communication, practical problem-solving, and a shared responsibility for doing things right. If you enjoy working in a supportive environment where your contributions make a real difference, [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Site Management Lead (30h/ week up to full-time)
• Wien
Führungs-/ Leitungspositionen
[. .. ] European pioneer for integrated therapies for rare diseases and in critical care. To enhance our team in Vienna we are looking for a: We are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an experiencedand proactive Clinical Site Management Leadto oversee the operational management of clinical studies and ensurehigh standardsof quality, compliance, and collaboration with study sites and partners. What Your Day To Day Will Look Like Manage assigned clinical studies from site start-up through close-out Prepare and coordinate submissions to Competent Authorities and Ethics Committees Conduct co-monitoring visits to ensure patient safety, data integrity, and regulatory compliance Build strong relationships with CRO personnel, site staff, and internal study teams Support and oversee CROs and freelance CRAs Review and analyse clinical study data for accuracy and completeness Ensure availability and quality of essential site documents for the Trial Master File Forecast IMP supply [. .. ] smooth trial execution Your Qualifications And Experience Bachelors degree or higher in Life Sciences, Pharmacy, Medical Sciences, or a related field Minimum 5 years of experience as a Clinical Research Associate (CRA) or 2 years as a Senior CRA Strong knowledge of clinical trial conduct, regulatory requirements, and ICH-GCP Experience with submissions to Competent Authorities and Ethics Committees Experience with risk-based monitoring Willingness to travel (max. 30-irregular, but can be flexibly divided in the team) Fluent in English [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Potsdam, Brandenburg
[. .. ] Clinic Nurse Manager Department: Oncology Location: Canton-Potsdam Hospital Hours Per Week: 40 scheduled weekly hours Schedule: 8-hour day shifts, 8-4:30 pm, Monday-Friday SUMMARY Responsible for the
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>clinical management of assigned PPM Practice (s) servicing patients in and around SLH in St. Lawrence County, New York. Works collaboratively in dyad relationship with Practice Manager (s) / Coordinator (s) in the supervision and support of clinical care coordinators, LPNs and MAs. Collaborate with key function leaders at SLH such as Director of Quality, Director of Patient
Safety, and Director of Patient Experience. Responsible for the management of quality clinical standards for employed and contracted physicians, mid-levels (providers) and staff. RESPONSIBILITIES Regulatory and Quality Management Supervises and assures effective, high quality clinical activities within the medical office home. Cooperates with all providers and clinical staff in performance [. .. ] delivery of chemotherapeutic and biological agent administration in the inpatient setting. REQUIRED QUALIFICATIONS Graduate of accredited school of nursing with BSN required (may be waived for individual with diploma or
associate degree who demonstrates experience in management of clinical staff) . Current, unrestricted New York State Registered Professional Nursing license. PREFERRED QUALIFICATIONS Oncology experience, certification, and management experience preferred Minimum 1 year of supervisory experience; healthcare setting preferred Strong leadership, team-building, and employee engagement skills Proficient in Microsoft Office (Outlook, [. .. ]
▶ Zur Stellenanzeige
Job vor 7 Tagen bei Jobleads gefunden
Associate Director/ Director CMC Product Development (all genders) (fulltime, permanent)
• Ludwigshafen am Rhein, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] psychiatric care into realities. Join a global powerhouse with over 50, 000 employees worldwide, including 3, 000 in Germany, where your expertise will address tomorrows unmet medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs. As an Associate Director/ Director CMC Product Development you independently manage programs of various complexity utilizing a matrix approach. You lead Chemistry, Manufacturing and Controls (CMC) teams and Product Presentation and Device Strategy Teams (PPDST) of functional representatives from various departments and divisions for projects involving external collaboration partners per Pipeline Commercialization Model [. .. ] 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 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 acrossasset strategies. Make Your Mark By Representing all CMC areas [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADa M datasets, Tables, Figures, Listings and Analysis Submission content. Collaborates with study teams to ensure the quality and accuracy [. .. ] deliverables. Additional tasks: Collaborates with CR D staff regarding data analysis requests. Performs additional statistical analyses including but not limited to: support responses to regulatory agencies, generate integrated summary of safety and efficacy, support publications and presentations, support planning and reporting of clinical trials via exploratory analyses of available data, Position Qualifications and Experience Requirements: Education BSc in Computer Science, Mathematics, Statistics or related area with relevant experience Experience At least 5+ years of experience in either clinical programming and/or [. .. ] Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Senior Statistical Programmer jobs in Frankfurt, Hesse, Germany. Associate Principal Statistical Programmer (m/w/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 84960764 [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Business development and operational manager Germany/ North Europe
• Heidelberg, Baden- Württemberg
[. .. ] area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Reporting to the Associate Director Business Development Manager Europe, you will help in identifying new potential customers and/or unexplored markets and lead operational activities including team management at client site. Working closely with Associate Director and client service team to create new pipeline to drive increases in business and lead the operational tasks [. .. ] River is an early-stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20, 000 employees within 110 facilities in over 20 [. .. ]
Job am 05.03.2026 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 [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
Salaried GP with View to Partnership
• Schwyz
[. .. ] in March, Cambridgeshire. A Friendly practice with around 7, 500 Patientsand still growing. Riverside have a dedicated team consisting of a GP partner, Salaried GP, Nurse Practitioners, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Practice Nurses, Nurse Associate, HCAs aswell as good supportive administrative and management team who are committed toproviding high-quality care and support to our patients. As a Practice we also work with the Fenland PCN and this comprises of three other surgeriesin the area Main duties of the job Clinical Responsibilities Provide comprehensive, safe, effective primary medical care to registered patients Manage acute and chronic conditions in line with evidence-based practice and national/ local guidelines. Provide continuity of care and holistic management of patients Review and action clinical correspondence, pathology results, and hospital letters Prescribe in accordance with practice [. .. ] expectations within primary care Work towards increased involvement in leadership, management, or clinical lead roles in preparation for potential partnership. Other Responsibilities Comply with all practice policies, including health and safety, information governance, and equality and diversity. Undertake any other duties appropriate to the role, as agreed with the partners and practice manager Person Specification Qualifications and Registration (Essential) Full registration with the General Medical Council (GMC) Inclusion on the NHS England GP Performers List Evidence of ongoing appraisal and revalidation [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
[. .. ] highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 4, 270.14 [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
• Wien
[. .. ] highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 4, 270.14 [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Associate Director, Technical Operations-Studentjob. ch
• Couvet, Neuenburg
Führungs-/ Leitungspositionen
Associate Director, Technical Operations Overview Wu Xi App Tec is a trusted partner and contributor to the pharmaceutical and life sciences industries, providing R D and manufacturing services that [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] help advance healthcare innovation. With operations across Asia, Europe, and North America, we offer integrated, end-to-end services through our unique [. .. ] strong OSD Drug Product technical skills to ensure the successful transfer of Drug Products to the Couvet site, Switzerland. This includes the on-time-in-full supply of technical, registration, clinical, stability, and PPQ batches This position report to the Vice President, Head of Late-Stage Formulation R D and Commercialization, and Head of Business Development for China Qualifications Bachelor degree or above combined with 15+ years experience in a pharmaceutical execution and management position 10+ years experience of OSD DP [. .. ] and troubleshooting of production Technical working instruction (including batch records) of various manufacturing technologies to ensure the production operation is compliant with the GMP policy and to satisfy the highest safety standard. Support deviations by leveraging technical expertise, manufacturing experience, and investigation skills Provide technical trainings and seminars to personnel of other departments to promote the application of new manufacturing technologies, and to resolve any misconception and miscommunication. Accountable for process validation (PPQ) , including Continued Process Verification Accountable for cleaning [. .. ]
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Als Clinical safety associate verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
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Aktuell gibt es auf JobRobot 58 offene Stellenanzeigen für Clinical Safety Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Safety Associate Jobs?
Aktuell suchen 13 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:
- ICON (17 Jobs)
- Abb Vie (2 Jobs)
- IQVIA (2 Jobs)
- AOP Health (1 Job)
- Alimentiv (1 Job)
In welchen Bundesländern werden die meisten Clinical Safety Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Safety Associate Jobs werden derzeit in Hessen (8 Jobs), Sachsen-Anhalt (7 Jobs) und Bayern (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Safety Associate Jobs?
Clinical Safety Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
