178 Jobs für Clinical Quality Associate
Stellenangebote Clinical Quality Associate Jobs
Job am 27.02.2026 bei StepStone gefunden
MED- EL Medical Electronics
• Innsbruck
Führungs-/ Leitungspositionen
[. .. ] of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 3, 100 employees around the [...]
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[...] world. CEO12602 Associate, Reimbursement HTA (m/f/d) CEO Team/Administration Innsbruck, Austria Professionals Full-Time 38.5h Permanent Active contribution to international projects in the areas of reimbursement and market access, including coordination, analysis, and substantive input on strategic topics Planning, conducting, and evaluating systematic literature searches, as well as structured evidence [. .. ] of the reimbursement landscape and performing analyses in the field of Health Technology Assessment (HTA) Bachelors degree or higher degree (University, FH) in Life Sciences, Public Health, Health Economics, or Clinical Research Excellent scientific writing skills, including experience with AI-assisted content development tools Very good English skills, both written and spoken; additional languages are an asset Proven ability to deliver high-quality analytical content Strong organizational skills with exceptional attention to detail Central Location Employee Discounts Flexible Hours International Environment Onboarding Workplace Well-Being Minimum Salary Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is 47, 810.14. . MED-EL Medical Electronics [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA
Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austria
• AT- 9 Wien
Homeoffice möglich
Join IQVIA Biotech as a
Clinical Research
Associate 2/ CRA 2 (m/w/d) to work home-based throughout Germany, and preferably in the Munich or Hamburg area. You will enjoy the stability [...]
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[...] and resources of a leading, global contract research organization while gaining direct experience with our clients. This role promises to offer intentional career growth and [. .. ] areas and in covering projects in Austria, Germany and/or Switzerland. Responsibilities Performing site selection, initiation, monitoring and closeout 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 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 [...]
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[...] 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 [. .. ] 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 well-[. .. ]
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 [...]
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[...] 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 [. .. ] 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 am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Position Summary A klinikai kutatsi asszisztens (
Clinical Research
Associate) felels a helyszni s tvoli monitori ltogatsok megtervezsrt s lebonyoltsrt, a vonatkoz szablyozsi normk (MDR, ISO 14155, ICH/ GCP irnyelvek, Teleflex [...]
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[...] eljrsok s IRB/ EC irnyelvek s eljrsok) elöirasainak megfelelen. A CRA a monitoring tervben, a kutatcsoport vagy az osztly ignyei szerint meghatrozza a monitoring ltogatsokat, hogy rtkelje az adatok [. .. ] the role involves travel. Working Environment Office Remote working. About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of peoples lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and [. .. ]
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 [...]
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[...] 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-[. .. ] remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance 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 [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
A leading
clinical research organization in Austria is seeking candidates for Clinical Research
Associate positions at various levels. The roles involve supporting site management through monitoring and initiation [...]
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[...] visits while ensuring data quality and compliance. Ideal candidates must hold an Honours Bachelors Degree with relevant experience ranging from 1 to 3 years depending on the level. The organization offers competitive compensation, including a base salary and performance bonuses, along with a comprehensive benefits package. J-18808-Ljbffr 83093352 [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
CRA single sponsor-Germany
• 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 [...]
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[...] 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 [. .. ] 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 [. .. ] 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. Impact and Contribution Individual 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 [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Octapharma Austria
• AT- 9 Wien
[. .. ] and development location. Your main tasks and responsibilites Act as scientific Subject Matter Expert within the lifecycle management of blood plasma products Collaborate crossfunctionally with Productions Sites, [...]
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[...] Manufacturing Science Technology, Quality, Regulatory Affairs, Business Units and other R D areas Lead and scientifically guide continuous process optimizations, process transfers, root cause analyses of investigations, change requests, submissions and inquiries from internal and external stakeholders Manage, coordinate, perform and continuously improve multiple complex lab operations and analytical tasks Critically coach others in [. .. ] 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, 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 [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
Octapharma Pharmazeutika Produktionsges. m. b. H.
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
• AT- 9 Wien
[. .. ] and development location. Your main tasks and responsibilites Act as scientific Subject Matter Expert within the lifecycle management of blood plasma products Collaborate crossfunctionally with Productions Sites, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Manufacturing Science Technology, Quality, Regulatory Affairs, Business Units and other R D areas Lead and scientifically guide continuous process optimizations, process transfers, root cause analyses of investigations, change requests, submissions and inquiries from internal and external stakeholders Manage, coordinate, perform and continuously improve multiple complex lab operations and analytical tasks Critically coach others in [. .. ] 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, 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 [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• 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 [...]
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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 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 [. .. ] 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. Discover what our more than 29, 000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting muchneeded therapies to those who need them most. A career with Syneos Health means your everyday [. .. ]
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 [. .. ] 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 [. .. ] 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. Impact and Contribution: Individual 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 [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
allaboutvienna
• 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 06.02.2026 bei Mindmatch.ai gefunden
IQVIA LLC
Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austria
• AT- 9 Wien
Homeoffice möglich
Clinical Research
Associate 2 (m/w/d) , IQVIA Biotech, based in Austria page is loaded # # Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austrialocations: Vienna, [...]
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[...] Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1526950External Job Description Join IQVIA Biotech as a Clinical Research Associate 2/ [. .. ] projects in Austria, Germany and/or Switzerland. 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 31.01.2026 bei Mindmatch.ai gefunden
Monte Rosa Therapeutics, Inc
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] The role will broadly support Monte Rosa Therapeutics (MRTx) global contracting function and requires substantial experience in drafting, reviewing and negotiating a wide range of agreements spanning [...]
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[...] research and development, clinical development, business development and general and administrative matters. Responsibilities Independently draft, review and negotiate a wide range of contracts including without limitation Confidential Disclosure Agreements, Master Service Agreements and associated Statements of Work, Consulting Agreements, License and Collaboration Agreements, Quality Agreements, Material Transfer Agreement, Clinical Trial Agreements and Informed Consent Forms based on MRTx templates and where necessary, evaluating third party agreements against MRTxs legal and business standards; Subject Matter Expertise with deep experience in working with Contract Development and Manufacturing Organizations to support CMC efforts and Contract Research Organizations [. .. ]
Job am 08.01.2026 bei Mindmatch.ai gefunden
Monte Rosa Therapeutics, Inc
Associate Director/ Director, Drug Product-CMC
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
Overview Monte Rosa Therapeutics (MRT) seeks to recruit an
Associate Director/ Director Drug Product CMC to play a key role in advancing our drug product development programs from early-stage [...]
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[...] development through commercialization. The successful candidate will join the CMC group supporting Monte Rosas portfolio of molecular glue degraders (MGDs) that eliminate disease-causing proteins previously thought undruggable. The Associate Director/ Director drug product (DP) will lead technical development activities related to formulation design, drug product development, manufacturing and clinical supply for Monte Rosa growing pipeline. This individual will be part of the CMC group and work cross-functionally with analytical, drug substance, quality, clinical operations and regulatory to ensure development of robust and phase appropriate supply strategies across the product lifecycle from early phases to late stages. Strong experience in Drug Product development of small molecule APIs spanning from early to late phase, experience in outsourcing and CDMOs management, the desire to work [. .. ]
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 [...]
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[...] 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 [. .. ] 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 (CQMP) . Aligns CQMP with IQRMP-identified risks and mitigations. Protocol Deviations Management: Provides medical [. .. ]
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 [. .. ] 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 (CQMP) . Aligns CQMP with IQRMP-identified risks and mitigations. Protocol Deviations Management Provides medical [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
• München, Bayern
Medical Science Liaison Complement-Mediated Diseases Seniority level
Associate Employment type Full-time Job function Other Pharmaceutical Manufacturing At Sobi, each person brings their unique talents to work as a team [...]
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[...] and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes [. .. ] engagement, medical scientific projects and scientific communications. 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 [. .. ] , D. N. P. , Ph. D. , or M. D. / D. O. ) . Consideration will be given to candidates with an advanced health degree and extensive industry or clinical experience. Ability to understand and effectively communicate scientific information; respond to inquiries and address needs of key stakeholders. A minimum of 1 year of MSL experience. Demonstrated success managing internal/ external stakeholders and leading or influencing cross-functional teams in a matrixed environment including strong teamwork and collaboration. Proven track [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Business Consultant-R D (Remote)
• 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 [...]
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[...] 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. [. .. ] 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Associate Director, Drug Substance Development (Home Based/Remote) 12 Month FTC
Führungs-/ Leitungspositionen
[. .. ] or membership, authoring technical reports and CMC sections of regulatory dossiers, and participation in department or functional initiatives. The role will involve significant cross functional collaboration with [...]
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[...] other functions including Quality, CMC Regulatory, Manufacturing, and New Product Technology Integration working towards agile new product introduction and ensuring all processes are understood, robust, efficient and in control. The role is both project and operations orientated. It shall require an ability to drive and deliver multiple projects concurrently. Responsibilities Lead the process development and c GMP manufacture of small molecule drug substances at CDMOs Ensure adequate supply of drug substance for clinical studies and other needs. Oversee the development of robust and reliable manufacturing processes utilizing Quality by Design (Qb D) principles. Oversee the synthesis of chemical entities to support clinical and non-clinical studies. Ensure that all DS processes are in line with all applicable regulations, policies, guidelines, and procedures. Represent the [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Director, Europe Patient Advocacy, Professional Relations, and Patient Engagement
• Zürich Zuerich
Führungs-/ Leitungspositionen
[. .. ] of people with cancer. We are seeking a team-oriented, results-driven professional committed to outstanding collaboration and passionate about strengthening the patient voice in Genmabs decision-making. The Director/ [...]
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[...] Associate Director, Patient Engagement Professional Relations (Europe) will lead and advance patient and professional engagement activities across Europe, ensuring the European patient voice is meaningfully represented in Genmabs strategy and decision-making, while partnering closely with global colleagues and alliance partners. Responsibilities European strategy planning Develop and execute a Europe-wide [. .. ] insights, preference research, PRO strategy, qualitative research, and engagement around value narratives) . o Help translate patient insights into HTA-relevant outputs (e. g. , unmet need articulation, treatment burden, quality-of-life impacts, caregiver impact, and patient journey insights) and ensure internal teams can use them effectively and compliantly. o Coordinate (as appropriate) patient input opportunities that may support HTA readiness (e. g. , advisory boards, structured interviews, workshops) and ensure feedback loops back to participating organizations and internal stakeholders. [. .. ] privacy requirements, and Genmab policies. Bring the European patient voice into Genmab Identify, design, and deliver innovative approaches to incorporate European patient insights into Genmab decision-makingespecially with Medical Affairs, Clinical Development, Regulatory, Market Access/ HEOR, Marketing/ Commercial, and Alliance colleagues. Translate patient insights into actionable recommendations and ensure feedback loops back to participating organizations and internal stakeholders. Governance, compliance, and privacy (Europe) Ensure all activities align with applicable European and local requirements and industry codes (e. g. , EFPIA and [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austria
• Wien
Homeoffice möglich
Join IQVIA Biotech as a
Clinical Research
Associate 2/ CRA 2 (m/w/d) to work home-based throughout Germany, and preferably in the Munich or Hamburg area. You will enjoy [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the stability and resources of a leading, global contract research organization while gaining direct experience with our clients. This role promises to offer intentional career growth and [. .. ] areas and in covering projects in Austria, Germany and/or Switzerland. Responsibilities Performing site selection, initiation, monitoring and closeout 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 gestern bei Jobleads gefunden
Associate Director, Biostatistics
• Zürich Zuerich
Führungs-/ Leitungspositionen
The
Associate Director (AD) , Biostatistics, leads the full scope of statistical contribution to a
clinical development program. The AD provides statistical strategies for the clinical trials and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory submissions, and is accountable for the statistical deliverables within the program. 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 [. .. ] Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations. Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions. Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. Manage outsourcing operations or work with internal statistical programmers within [. .. ]
Job gestern bei Jobleads gefunden
Director, Europe Patient Advocacy, Professional Relations, and Patient Engagement
• Zug
Führungs-/ Leitungspositionen
[. .. ] of people with cancer. We are seeking a team-oriented, results-driven professional committed to outstanding collaboration and passionate about strengthening the patient voice in Genmabs decision-making. The Director/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate Director, Patient Engagement Professional Relations (Europe) will lead and advance patient and professional engagement activities across Europe, ensuring the European patient voice is meaningfully represented in Genmabs strategy and decision-making, while partnering closely with global colleagues and alliance partners. Responsibilities European strategy planning Develop and execute a Europe-wide [. .. ] patient insights, preference research, PRO strategy, qualitative research, and engagement around value narratives) . Help translate patient insights into HTA-relevant outputs (e. g. , unmet need articulation, treatment burden, quality-of-life impacts, caregiver impact, and patient journey insights) and ensure internal teams can use them effectively and compliantly. Coordinate (as appropriate) patient input opportunities that may support HTA readiness (e. g. , advisory boards, structured interviews, workshops) and ensure feedback loops back to participating organizations and internal stakeholders. Ensure [. .. ] privacy requirements, and Genmab policies. Bring the European patient voice into Genmab Identify, design, and deliver innovative approaches to incorporate European patient insights into Genmab decision-makingespecially with Medical Affairs, Clinical Development, Regulatory, Market Access/ HEOR, Marketing/ Commercial, and Alliance colleagues. Translate patient insights into actionable recommendations and ensure feedback loops back to participating organizations and internal stakeholders. Governance, compliance, and privacy (Europe) Ensure all activities align with applicable European and local requirements and industry codes (e. g. , EFPIA and [. .. ]
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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 178 offene Stellenanzeigen für Clinical Quality Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Quality Associate Jobs?
Aktuell suchen 30 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:
- MEDPACE (21 Jobs)
- ICON (18 Jobs)
- Astra Zeneca (12 Jobs)
- IQVIA (9 Jobs)
- Herman Medical Staffing GmbH (3 Jobs)
- Optimapharm d. o. o. (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Quality Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Quality Associate Jobs werden derzeit in Hessen (19 Jobs), Sachsen-Anhalt (19 Jobs) und Bayern (17 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Quality Associate Jobs?
Clinical Quality Associate Jobs gehören zum Berufsfeld Qualitätswesen.
