142 Jobs für Clinical Quality Associate
Stellenangebote Clinical Quality Associate Jobs
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Jazz Pharmaceuticals
• Munich Muenchen
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
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[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree [. .. ] alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the German Oncology Medical Affairs field strategy and plan in close collaboration with business partners and aligned to the EU/ INT strategy Ensure the transfer of field insights into the appropriate [. .. ]
Job vor 3 Tagen bei JobMESH gefunden
Jazz Pharmaceuticals
Associate Director, Head of MSL Oncology, Germany
• Bavorsko Mnichov
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
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[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree [. .. ] alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the German Oncology Medical Affairs field strategy and plan in close collaboration with business partners and aligned to the EU/ INT strategy Ensure the transfer of field insights into the appropriate [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
ICON
• 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 [...]
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[...] 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, [. .. ] 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 or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
Clinical Trial Associate
• AT- 8 Gemeinde Au
Work-Life-Balance
Overview
Clinical Trial Assistant-Office-based in Sydney 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 [...]
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[...] welcome you to join us on our mission to shape the future of clinical development. What you will be [. .. ] and guidelines. Excellent organizational and communication skills. Ability to work collaboratively in a fast-paced environment with attention to detail. What ICON can offer you Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
• 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 [...]
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[...] 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, [. .. ] travel at least 60 of the time (international and domestic-fly and drive) and should possess a valid drivers license. What ICON can offer you Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on wellbeing [. .. ]
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 [...]
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[...] 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 [. .. ] time (international and domestic-fly and drive) and should possess a valid drivers license. #LI-KA1 #LI-Remote What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on wellbeing [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
• 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 [...]
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. We are currently seeking [. .. ] travel at least 60 of the time (international and domestic fly and drive) and should possess a valid drivers license. What ICON can offer you Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on wellbeing [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Takeda
Associate Director, API Process Engineering
• AT- 9 Wien
Führungs-/ Leitungspositionen
About the role As
Associate Director, API Process Engineering, you will be Takedas global expert for smallmolecule API manufacturing processes across batch and continuous platforms. You will apply chemical [...]
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[...] engineering and process chemistry fundamentals to design, scale, and control API processes from clinical development through commercial supply. Through the integration of mechanistic modelling, process simulation, and rigorous data analysis you will deepen process understanding, strengthen control strategies, and support regulatory submissions for global markets. You will become the central hub for API process knowledge, driving best practices and continuous improvement across Takedas manufacturing [. .. ] learned are shared across products, sites, and functions. Collaborate closely with GMS functions (e. g. , Small Molecules Operations Units, network strategy) , site leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC. Provide technical support to marketing applications for global markets and lead preparation of responses to regulatory questions from health authorities. Utilize structured root cause analysis techniques to investigate process and equipment issues and deliver robust, sustainable corrective and preventive actions. Provide subject matter expertise for due diligence [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Takeda
• AT- 4 Linz
Führungs-/ Leitungspositionen
About the role As
Associate Director, API Process Engineering, you will be Takedas global expert for smallmolecule API manufacturing processes across batch and continuous platforms. You will apply chemical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engineering and process chemistry fundamentals to design, scale, and control API processes from clinical development through commercial supply. Through the integration of mechanistic modelling, process simulation, and rigorous data analysis you will deepen process understanding, strengthen control strategies, and support regulatory submissions for global markets. You will become the central hub for API process knowledge, driving best practices and continuous improvement across Takedas manufacturing [. .. ] learned are shared across products, sites, and functions. Collaborate closely with GMS functions (e. g. , Small Molecules Operations Units, network strategy) , site leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC. Provide technical support to marketing applications for global markets and lead preparation of responses to regulatory questions from health authorities. Utilize structured root cause analysis techniques to investigate process and equipment issues and deliver robust, sustainable corrective and preventive actions. Provide subject matter expertise for due diligence [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
allaboutvienna
Healthcare Medical
• AT- 9 Wien
[. .. ] 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 [...]
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[...] 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 [. .. ] and innovation. For a behind-the-scenes look, check out this. . . Permanent Austria-Wien 9 hours ago Were looking for a passionate QA Engineer Are you driven by quality and eager to contribute to impactful digital solutions? Join a dynamic and collaborative Agile environment where your work will. . . Permanent Abbvie Austria-Wien 9 hours ago Head of Medical Specialty Care PRIMARY FUNCTION Lead the Therapeutic Areas (Eyecare, Neuroscience and Neurotoxins) specific staff and activities and provide leadership, [. .. ] 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 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
• 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 [...]
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[...] 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 [. .. ] studies by monitoring data and processes from a centralized location. They conduct remote and onsite monitoring, automate data analytics and riskbased monitoring, and collaborate with site teams to implement effective quality monitoring processes that support successful clinical trials. Employment Details Seniority level: Mid Senior level Employment type: Fulltime Job function: Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x. Get notified about new Clinical Research Associate jobs in Vienna, Vienna, Austria. EEO Statement The [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
i- Pharm Consulting
Clinical Research Associate
• AT- 9 Wien
Work-Life-Balance
Job Title:
Clinical Research
Associate (CRA) 0.8 FTE Location: Austria Duration: 12-Month Contract Travel: 6080 About the Company Join a leading global contract research organization (CRO) that partners [...]
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[...] with pharmaceutical, biotechnology, and medical device companies to advance innovative therapies. The organization is known for its commitment to high-quality clinical research and supports employees in professional growth and development while contributing to meaningful medical advancements worldwide. Role Overview We are seeking an experienced Clinical Research Associate (CRA) to manage and coordinate clinical trial site activities in Austria on a 12-Month Contracted basis. In this role, you will ensure [. .. ]
Job am 02.11.2025 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Homeoffice möglich
Join IQVIA as a
Clinical Research
Associate I or II (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. Youll enjoy [...]
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[...] the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether youre just starting out or [. .. ] in a wide variety of therapeutic areas. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Collaborating with experts at study sites and with client representatives [. .. ]
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 [...]
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[...] 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 [. .. ] 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 [. .. ] identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Induvidual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the [. .. ]
Job am 06.11.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline [...]
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[...] across preclinical and clinical development. We are driven by science with a patientcentric and teamoriented culture. This is an exciting time to join Crinetics as we shape our organization into the worlds premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others. Position Summary: [. .. ] the European Leadership team partnering crossfunctionally with other key stakeholders to assist the Company in achieving its purpose and goals in Germany. The Senior Director will work directly with the Associate General Counsel, Global Commercial Legal to support EU leaders on local Commercial Legal matters including promotional and Medical Affairs activities and materials, vendor and HCP contracts, market access issues, and other Commercial Legal matters consistent with Crinetics Global Commercial strategies and processes. The role also collaborates closely with the VP [. .. ] for managing legal matters, balancing inhouse and thirdparty work to minimise risk and manage the legal budget. Ensure compliance with industry codes of practice and applicable regulatory, privacy, pharmacovigilance, and quality requirements. Collaborate creatively with internal clients and other functions in a matrixed team environment. Lead special projects and participate in crossfunctional teams and committees. Stay informed of new laws, regulations, and industry trends affecting the organization and provide relevant training. Demonstrate indepth knowledge of pharmaceutical regulations, bribery and antikickback laws, [. .. ]
Job am 08.10.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Amyloidosis, North-Eastern Germany (Rostock, Berlin, Leipzig, . . .
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
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[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. This Is What You Will Do The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports [. .. ] to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and high-level therapeutic expertise. Train Alexion staff on [. .. ] Pharmaceuticals, Inc. by 2x Get notified about new Medical Science Liaison jobs in Munich, Bavaria, Germany. Scientific Affairs Manager-Germany (Southwest) Medical Affairs Manager Germany and Austria (f/m/d) Associate Director Medical Affairs (MSL Lead) Senior Manager (m/f/x) Medical Affairs QA Medical Science Liaison-National-Germany Medical Science Liaison Oncology/ Hematology (m/w/d) Medical Science Liaison Manager Neph, Süd-West Werkstudent, Medical Medical Affairs (m/w/d) Were unlocking community knowledge in a new way. Experts add [. .. ]
Job am 18.08.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] This person will proactively manage medical scientific stakeholders and create value for patients through medical and scientific stakeholder engagement, medical scientific projects and scientific communications. This role [...]
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[...] reports to the Associate Director Medical Science Liaison. Key Responsibilities: Identify, develop and maintain collaborative relationships with KOLs, scientific experts and other medical scientific stakeholders. Compile, analyze, prepare and deliver high quality medical pharmaceutical and scientific communications in line with defined communication plans. Create and execute stakeholder engagement plans, according to Sobis high standards. Support country Global Brand team in developing local medical tactics and provide input to Headquarter (HQ) / regional plans if relevant organize and set up scientific advisory boards [. .. ] Qualifications Education/ Learning Experience/ Work Experience Required: University degree in medical/ science or other relevant field +3 years of direct experience in the medical environment Experience from medical affairs, medical/ clinical science, clinical development, access and health economy Experience in hematology, oncology, immune thrombocytopenia, lymphoma In-depth knowledge of national healthcare systems and practices Experience in KOL Management and Account Planning Ability to create and network with KOLs at national level Experience working with KOLs within hematology, oncology, immune thrombocytopenia, lymphoma [. .. ]
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 INRALS [...]
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[...] (International Network of Recruitment Agencies in Life Sciences) , we are looking for an Associate Director Patient [. .. ] 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 [. .. ] involvement in regulatory submissions would be advantageous. Clinical or research experience in oncology are a big plus. Strong interpersonal and communication skills. Strong ethical sense coupled with a focus on quality and patient safety. Excellent English language skills, both written and verbal. BENEFITS: Highly strategic and development-related role. High-impact on the development of new drugs. Global and intercultural work environment. #J-18808-Ljbffr 55042181 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• 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 [...]
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[...] 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 [. .. ] 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 [. .. ] Experience in management of cutaneous toxicities of immunotherapy. Proven commitment to proactively keeping up to date with discipline knowledge and developments. Demonstrated track record in research with outcomes of high quality and high impact with clear evidence of a desire and ability to continually achieve research excellence as well as the capacity for research leadership. Demonstrated ability to work in a team, collaborate across disciplines and build effective relationships. Evidence of highly developed interpersonal and organisational skills. An understanding of and [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Associate Biostatistics Director-FSP (Permanent Home-based)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. Provide statistical thought partnership for innovative study design and clinical development plans, including Go No Go criteria and probability of technical success calculations. Provide projectwide planning of analyses; ensure quality and timely delivery of interim and final results, including integrated analyses for submissions. Represent Biostatistics in interactions with regulatory authorities (e. g. , FDA, EMA, PMDA) . Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. Prepare abstracts, posters, oral presentations and written [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Research Associate II (m/f/d) Belgium
• Stein, Baden- Württemberg
Its a good feeling to know youre doing your best with purpose every day. At Artivion, we manufacture high-
quality products and solutions for the treatment of aortic diseases. Together [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We are hiring a Clinical Research Associate II (m/f/d) Belgium Your Strength 18 months to 4 years of site monitoring experience in clinical research Ability to work independently with limited supervision Excellent understanding of GCP, ISO 14155, MDR, FDA, EU, and local clinical regulations Strong communication and relationship-building skills with investigators and site personnel [. .. ]
Job gestern bei Jobleads gefunden
Associate Director, Regulatory Affairs Strategy EMEAC
• Zug
Führungs-/ Leitungspositionen
Associate Director, Regulatory Affairs Strategy EMEAC Pay Competitive Employment type Full-Time Job Description Req #: ASSOC001754 Join Us Reata Pharmaceuticals As a commercial pharmaceutical company, we are committed to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] positively impacting the lives of patients with life-threatening diseases. With rigorous science and research as our foundation, we are a [. .. ] to the development, registration and maintenance of Reatas product portfolio across the EMEAC region. This role will support the development of regulatory product strategy and ensures the timely and high-quality execution of the EMEA regulatory strategy. Key Responsibilities Participate in the development of regulatory strategies and tactical plans for the assigned products in collaboration with cross-functional teams Work closely with the GRL and departments area Operations, Submission Management, CMC, and Commercial Support) and be an active member of the [. .. ] quality regulatory dossiers (scientific advice requests, orphan medicinal product designation applications, pediatric investigational plans, MAAs, variations and responses to HA questions) ensuring compliance with regulatory requirements Be a member of clinical trial teams and coordinates CTA related activities Ensure effective coordination of the interactions with the European Medicinal Agency (EMA) , and National Regulatory Health Authorities Make sure that relevant internal teams, at global and EMEAC level, are kept updated in a timely manner, on regulatory product plans, progress and operational [. .. ]
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 [. .. ] reaction execution platforms, liquid handlers, parallel autoclaves) . Contribute to the continuous improvement of automation workflows 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 [. .. ]
Job gestern bei Jobleads gefunden
Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Manager or
Associate Principal, EMEA Life Science Strategy Supply Operations Consulting page is loaded # # Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consultingtime type: Full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] timeposted on: Posted Todayjob requisition id: R1457456Manager/ Associate Principal, EMEA Strategy Supply Operations Consulting Location: Munich or Basel Solution Area: Operations Consulting, Life Sciences [. .. ] about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. Were purpose-driven [. .. ] # # Key Responsibilities Project Management: Manage end-to-end delivery of consulting projects in the supply chain/ operations domain. Develop work plans, manage timelines and resources, and ensure high-quality outputs. Coordinate closely with client teams to gather data, provide updates, and drive implementation of recommendations. Client Advisory: Serve as a trusted advisor to client stakeholders at the project level, building strong working relationships. Understand clients operational pain points and objectives; translate them into project scopes and solutions. Present findings [. .. ]
Job gestern bei Jobleads gefunden
Associate Director, Pharmacometrics
Führungs-/ Leitungspositionen
[. .. ] end platform with biosimulation, regulatory science, and market access solutions combined with our strong team of scientists and subject matter experts enable our clients to have informed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] decision-making, reduced clinical trial burden, higher R D productivity, improved patient outcomes and increased patient access to medicines, and accelerated regulatory approval. Informed decision-making reduced clinical trial burden Higher R D productivity Improved patient outcomes increased patient access to medicines Accelerated regulatory approval Certara is a global team that nurtures a diverse [. .. ] projects for Certaras clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands-on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in Bioengineering, Pharmaceutical [. .. ]
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Wieviel verdient man als Clinical quality associate pro Jahr?
Als Clinical quality associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Quality Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 142 offene Stellenanzeigen für Clinical Quality Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Quality Associate Jobs?
Aktuell suchen 16 Unternehmen nach Bewerbern für Clinical Quality Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Quality Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Quality Associate Stellenangebote:
- Astra Zeneca (15 Jobs)
- Planet Pharma (10 Jobs)
- ICON (5 Jobs)
- IQVIA (5 Jobs)
- ICON Strategic Solutions (4 Jobs)
- Herman Medical Staffing GmbH (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Quality Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Quality Associate Jobs werden derzeit in Bayern (16 Jobs), Berlin (13 Jobs) und Baden-Württemberg (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Quality Associate Jobs?
Clinical Quality Associate Jobs gehören zum Berufsfeld Qualitätswesen.
