Clinical Support Associate Stellenangebote


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Stellenangebote Clinical Support Associate Jobs


Job vor 6 Tagen bei Mindmatch.ai gefunden MED- EL

Clinical Support Associate (m/w/d)

• AT- 7 Innsbruck Flexible Arbeitszeiten VCS12512 Innsbruck, Österreich Fachkräfte Vollzeit 38, 5 h Das VIBRANT Clinical Support Team fungiert als Schnittstelle zwischen Medizin, Technik und unseren Kund innen. Unter anderem werden medizinische Fachpersonen geschult und [...]
MEHR INFOS ZUM STELLENANGEBOT[...] bei der Nutzung unserer VIBRANT Hörlösungen im klinischen Alltag unterstützt. Ihre Aufgaben Unterstützung unserer weltweiten Niederlassungen, Distributoren, Kliniken und Patient innen Technischer Support sowie umfassendes Wissen über Mittelohrimplantate (VIBRANT SOUNDBRIDGE und PMEIs) [. .. ]

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Job vor 2 Tagen bei StepStone gefunden Otsuka Pharma GmbH Associate Director Global Regulatory Affairs (m/f/d) • Frankfurt am Main Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten [. .. ] to make a difference together For Otsuka Pharma Gmb H in the department Global Regulatory Affairs we are looking for a full-time employee to start as soon [...]
MEHR INFOS ZUM STELLENANGEBOT[...] as possible as Associate Director Global Regulatory Affairs (m/f/d) The Associate Director Regulatory Affairs provides global regulatory expertise to pre-clinical, clinical, and commercial areas for investigational and marketed products and he ensures that regulatory/ competitive intelligence, or scientific/ regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. Furthermore the Associate Director Regulatory Affairs collaborates with Regulatory Management to establish clear regulatory pathways and creates accurate and [. .. ] contact to Competent Authorities within Europe and other regions as required Identifying the need and obtaining regulatory intelligence, researching precedent approvals and prior health authority decisions to assess applicability to support development of strategic options for assigned Otsuka products Translating complex pertinent global requirements and providing an assessment of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/ external functional business units as needed Leading a cross functional team to collaboratively develop a global regulatory [. .. ]

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Job am 27.02.2026 bei StepStone gefunden MED- EL Medical Electronics

Associate, Reimbursement HTA (m/f/d) CEO Team/Administration

• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 synthesis to support HTA dossiers and market access strategies Preparation of clear project documentation and internal reports that present complex information in a concise, comprehensible, and audience-appropriate manner Conducting assessments 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 [. .. ]

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Neu Job vor 4 Std. bei Mindmatch.ai gefunden Intuitive da Vinci Clinical Territory Associate (m/w/d) • AT- 9 Wien [. .. ] a life. If youre ready to contribute to something bigger than yourself and help transform the future of healthcare, youll find your purpose here. Stellenbeschreibung Primary Function [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Of Position The Clinical Territory Associate (CTA) will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our business to include technical, clinical, and sales. He or she will train to be a da Vinci Surgery technical and sales expert across all primary surgical specialties to develop surgical robotics programs in [. .. ] and during the second year of the job, the CTA will progress and begin to focus on the sales aspect of the job. The CTA will have the opportunity to support a specific region by maximizing the utilization of installed da Vinci Surgical Systems by leading product demonstrations/in-services and sales activities. This position is an entry level position as well as a developmental role. Roles And Responsibilities Case Support-be a resource to the surgical team by providing guidance, [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ] 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. Mentoring less experienced team members, support as subject matter expert for specific topics or additional tasks might be included. Qualifications University Degree in life science or other scientific discipline or apprenticeship in the health care field. Minimum of two years of onsite monitoring experience alternatively an equivalent combination of education, training and experience. Knowledge of applicable [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden ICON Senior CRA • 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 [. .. ] 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 teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 and oversee drug accountability Provide training to CROs and study staff on study protocols and procedures Support the [. .. ] 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 [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden ICON Senior Clinical Research Associate Global Trial Oversight • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] an advanced 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 [. .. ]

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Job am 11.03.2026 bei Mindmatch.ai gefunden Alimentiv

Clinical Research Associate Eastern Europe (ISr)

• AT- 9 Wien A clinical research firm is inviting qualified candidates to join their talent pool for Clinical Research Associate roles across various seniority levels. Responsibilities include site management, data review, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] training support, and query resolution. Candidates with 13 years of experience in clinical research and an Honours Bachelor Degree are sought after. The company offers a comprehensive benefits package, including base salary and performance bonuses. J-18808-Ljbffr 83945563 [. .. ]

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Job am 11.03.2026 bei Mindmatch.ai gefunden Teleflex Clinical Research Associate • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] irnyelvek, Teleflex 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 [. .. ] be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community. If you require accommodation and support to apply for a position, please contact us at Diversity fosters innovative thinking and entrepreneurship and thats what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror [. .. ]

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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-note that this Talent Pool is not [. .. ]

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Job am 06.03.2026 bei Mindmatch.ai gefunden MED- EL Associate, Reimbursement HTA (m/f/d) • AT- 7 Innsbruck [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] evidence synthesis to support HTA dossiers and market access strategies Preparation of clear project documentation and internal reports that present complex information in a concise, comprehensible, and audience-appropriate manner Conducting assessments of the reimbursement landscape and performing analyses in the field of Health Technology Assessment (HTA) Your Profile 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 highquality analytical content Strong organizational skills with exceptional attention to detail Your Benefits Central Location Employee Discounts Flexible Hours International [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ] Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ] 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 [. .. ]

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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 [. .. ] of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11, 000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R D sites and five stateoftheart manufacturing facilities in Austria, France, Germany and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades [. .. ]

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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 [. .. ] 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 [. .. ] of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11, 000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R D sites and five stateoftheart manufacturing facilities in Austria, France, Germany and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades [. .. ]

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Job am 22.02.2026 bei Mindmatch.ai gefunden Syneos Health, Inc. CRA: Remote On-site Clinical Monitoring Pro • AT- 9 Wien A leading biopharmaceutical solutions organization in Vienna is seeking a Clinical Research Associate to oversee clinical trials ensuring compliance and data integrity. Responsibilities include site qualification, monitoring, and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] documentation while providing superior patient support. Ideal candidates possess a degree in a related field, knowledge of clinical guidelines, and fluency in German. This role offers opportunities for personal and professional growth in a dynamic and inclusive work environment. J-18808-Ljbffr 81482935 [. .. ]

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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 [. .. ] Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ] 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 [. .. ]

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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 [. .. ] Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ] 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 [. .. ]

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Job am 22.02.2026 bei Mindmatch.ai gefunden allaboutvienna

Healthcare Medical

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

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Job 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, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1526950External Job Description Join IQVIA Biotech as a Clinical Research Associate 2/ [. .. ] by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts at study sites and with client representatives. Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included. Qualifications: University Degree in life science or other scientific discipline or apprenticeship in the health care field. Minimum of two years of on-site monitoring experience alternatively an equivalent combination of education, training and experience. Knowledge of [. .. ]

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Job am 31.01.2026 bei Mindmatch.ai gefunden Monte Rosa Therapeutics, Inc Associate Director, CMC-Contracts Management • AT- 2 Schweiz Führungs-/ Leitungspositionen [. .. ] Management must thrive in a dynamic, high-performing and collaborative environment, demonstrating a proven ability to work cross-functionally as a trusted, solutions-oriented business partner. The role will broadly [...]
MEHR INFOS ZUM STELLENANGEBOT[...] support Monte Rosa Therapeutics (MRTx) global contracting function and requires substantial experience in drafting, reviewing and negotiating a wide range of agreements spanning 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ] and define formulation strategies based on chemico-physical. Work closely with drug substance experts to define suitable development strategies and plan related activities. Supply drug product through external vendors to support preclinical (PK studies, etc) and clinical studies. Hands on management of scale-up of tox formulation and supply related material. Directly manage and supervise work at external vendors including process development, scale-up, manufacturing trouble shooting and material supply with high level of independence. Identify, select and manage with high [. .. ]

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Job am 15.02.2026 bei Jobleads gefunden MEDICAL DIRECTOR Führungs-/ Leitungspositionen Doctors Health SA (DHSA) is a notforprofit company with the mission of improving the health of the medical profession for the good of the community. It achieves this by offering [...]
MEHR INFOS ZUM STELLENANGEBOT[...] clinical, education, training and phone advisory services exclusively to medical students and doctors. DHSA has delivered clinical services to over 20 of the profession through its unique afterhours assessment clinic. They focus on comprehensive afterhours checkups as well as acute medical care, delivered by a team of experienced GPs. They coordinate [. .. ] students and from which doctors and students can access a GP for their ongoing primary care. The Medical Director is the public face of the organisation and provides guidance and support to the Business Manager and Program Manager with the aim of delivering an integrated suite of educational and clinical activities. The MD also oversees the provision of safe, highquality, timely clinical care to patients presenting at the clinic, the 24/ 7 phone service, and the rural outreach programmes. Key Outcomes [. .. ] and national police clearance are essential. An appropriate level of remuneration will be agreed with the successful candidate. A Position Description can be found at. For further enquiries, contact VUCA Associate, Megan Galpin on 0402 224 800 for a confidential discussion during business hours. Please forward your letter of application and CV in MS Word format to emailprotected by COB Monday 23 February 2026. #J-18808-Ljbffr 80798892 [. .. ]

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Job am 11.12.2025 bei Jobleads gefunden Medical Science Liaison Complement-Mediated Diseases • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ] 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 with the appropriate key stakeholders, in collaboration with Medical Advisor or Senior Medical Advisor (MA, SMA) . Contribute and support medical scientific aspects [. .. ] , 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 [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden Business Consultant-R D (Remote) • Berlin Beratungs-/ Consultingtätigkeiten [. .. ] made history in 2021 by becoming a public benefit corporation (PBC) , legally bound to balancing the interests of customers, employees, society, and investors. As a Work [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment. Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities. The Role We are seeking talented individuals to join the Veeva Business [. .. ] 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 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 [. .. ] 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 [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Clinical Support Associate pro Jahr?

Als Clinical Support Associate verdient man zwischen EUR 35.000,- bis EUR 50.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Support Associate Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 201 offene Stellenanzeigen für Clinical Support Associate Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Support Associate Jobs?

Aktuell suchen 38 Unternehmen nach Bewerbern für Clinical Support Associate Jobs.


Welche Unternehmen suchen nach Bewerbern für Clinical Support Associate Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Support Associate Stellenangebote:


  • ICON (19 Jobs)
  • IQVIA (9 Jobs)
  • Intuitive (7 Jobs)
  • Optimapharm d. o. o. (3 Jobs)
  • MED- EL (2 Jobs)


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

Die meisten Stellenanzeigen für Clinical Support Associate Jobs werden derzeit in Bayern (26 Jobs), Hessen (20 Jobs) und Sachsen-Anhalt (19 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Support Associate Jobs?

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


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