45 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Description On-site
monitor open to diverse EMEA countries. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
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[...] 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 [. .. ] all remote and on-site monitoring activities through all study stages. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and SMP, within required timelines. [. .. ]
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 an advanced [...]
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[...] degree in a relevant field and extensive experience in clinical trial processes. You will monitor trial sites, conduct site visits, and collaborate with teams to ensure data integrity and participant safety. ICON offers a competitive salary and comprehensive benefits to support work-life balance. J-18808-Ljbffr 85227186 [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
Greiner
• KI Kremsmünster
Stellenbeschreibung Your challenge Collaborate with a
clinical project team to establish project objectives and timelines for IVd/MD trials Conduct of IVD and MD studies in accordance with the protocol, standard [...]
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[...] operating procedures, ISO 14155 GCP, Regulation (EU) 2017/ 745 (medical devices) , Regulation (EU) 2017/ 746 (IVDs) and Medical Devices Act Trial sites feasibilities Performance of site initiations, on-site monitoring, monitoring GB Olab, remote monitoring and closeout visits Training of study team members in accordance with protocol specific requirements and (local) regulations Ensuring the accuracy, validity and completeness of study data Support the (international) trials submission to authorities and ethics committees [. .. ] Your profile University degree in biology, medicine, pharmacy or an equivalent combination of education, training and work experience in clinical trials At least 2 years of experience as a clinical monitor (CRA) in a CRO/ medical device or pharmaceutical company Good knowledge of current industry practices related to the conduct of clinical studies (ICHGCP, ISO 14155, ISO 20916) Good knowledge of MDR and IVDR and a good understanding of GDPR Experience of FDA, ISO regulations and CLSI guidelines is an advantage [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
Greiner
Clinical Monitoring Specialist Remote/ Travel Ready
• KI Kremsmünster
A leading medical technology company is seeking a skilled
Clinical Monitor to oversee IVd/MD trials in Kremsmünster, Austria. The ideal candidate will bring at least two years of clinical
trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience and must be fluent in German. Responsibilities include collaborating with project teams, ensuring compliance with regulations, and managing study data. The role can be performed remotely or on-site, offering a competitive salary starting at EUR 59, 781.96, with potential overpayment based on experience. J-18808-Ljbffr 83341968 [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Greiner Bio- One International
Clinical Monitoring (all genders)
• KI Kremsmünster
Your challenge Collaborate with a
clinical project team to establish project objectives and timelines for IVd/MD trials Conduct of IVD and MD studies in accordance with the protocol, standard operating [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] procedures, ISO 14155 GCP, Regulation (EU) 2017/ 745 (medical devices) , Regulation (EU 2017/ 746 (IVDs) and Medical Devices Act Trial sites feasibilities Performance of site initiations, on-site monitoring, monitoring GBO-lab, remote monitoring and close-out visits Training of study team members in accordance with protocol specific requirements and (local) regulations Ensuring the accuracy, validity and completeness of study data Support the (international) trials submission to authorities and ethics [. .. ] Your profile University degree in biology, medicine, pharmacy or an equivalent combination of education, training and work experience in clinical trials At least 2 years of experience as a clinical monitor (CRA) in a CRO/ medical device or pharmaceutical company Good knowledge of current industry practices related to the conduct of clinical studies (ICH-GCP, ISO 14155, ISO 20916) Good knowledge of MDR and IVDR and a good understanding of GDPR Experience of FDA, ISO regulations and CLSI guidelines is an [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
NEVEON Executive Committee
Remote Clinical Monitoring Specialist (IVd/Medical Devices)
• KI Kremsmünster
A leading
clinical research organization in Austria is seeking an experienced Clinical
Monitor to oversee IVD and MD trials. The role involves collaboration with project teams, conducting studies, ensuring data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accuracy, and liaising with trial sites. Candidates should have at least 2 years of experience, a university degree in a relevant field, and be fluent in German. A modern and collegial working environment is offered, along with a base salary of EUR 59, 781.96, with the potential for overpayment based on qualifications. J-18808-[. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
NEVEON Executive Committee
Clinical Monitoring (all genders)
• KI Kremsmünster
[. .. ] and MD studies in accordance with the protocol, standard operating procedures, ISO 14155 GCP, Regulation (EU) 2017/ 745 (medical devices) , Regulation (EU 2017/ 746 (IVDs) and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Devices Act Trial sites feasibilities Performance of site initiations, on-site monitoring, monitoring GBO-lab, remote monitoring and close-out visits Training of study team members in accordance with protocol specific requirements and (local) regulations Ensuring the accuracy, validity and completeness of study data Support the (international) trials submission to authorities and ethics [. .. ] liaison between trialsites and sponsor Creation of study specific forms TMF maintenance Your profile University degree in biology, medicine, pharmacy or an equivalent combination of education, trainingand work experience in clinical trials At least 2 years of experience as a clinical monitor (CRA) in a CRO/ medical device or pharmaceutical company Good knowledge of current industry practices related to the conduct of clinical studies (ICH-GCP, ISO 14155, ISO 20916) Good knowledge of MDR and IVDR and a good understanding of GDPR Experience of FDA, ISO regulations and CLSI guidelines is an [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
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[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] on medical issuesproviding clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical [. .. ]
Job gestern bei Jobleads gefunden
• Lausanne, Waadt
[. .. ] recent brand launches and shaping the next phase of our product development. With strong results behind us, were moving ahead with pace and ambition. Leveraging your expertise [...]
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[...] in brain science, clinical trial methodology, and nutritional actives, you will ensure our products are grounded in rigorous science, clinically proven evidence, and aligned with regulatory and market expectations. This role will also act as the internal scientific authority, turning complex science into actionable insight to guide innovation, claims, and market positioning. Were looking for [. .. ] supporting proposed actives and associated health claims Identify evidence gaps and recommend appropriate study approaches (e. g. , clinical trials or consumer research) to validate product evidence and/or claims Monitor and assess emerging ingredients, technologies, and scientific trends relevant to brain health and nutrition Develop external partnerships and research collaborations, drawing on and expanding a strong professional network Serve as a scientific spokesperson internally and externally, supporting key stakeholders including Regulatory, Marketing, and regional business teams This highimpact role brings [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Director, Audit Strategy and Vendor Quality
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] you thought possible. About the Director, GCP Audit Strategy and Vendor Quality The Director is accountable for designing and executing a global, riskbased audit strategy to ensure [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance with Good Clinical Practice (GCP) requirements. The role drives robust vendor quality oversight across all clinical trial service providers in close partnership with Development Quality. It establishes and maintains a comprehensive vendor quality management framework for CROs and other external partners, including quality agreements, oversight plans, governance structures, and continuous improvement initiatives. Responsibilities Design and implement a global, riskbased GCP audit strategy aligned with ICH E6 (R3) [. .. ] Global Audit Plan. Establish and evolve the Vendor Quality and Third Party Risk Management (TPRM) strategy, ensuring consistent risk classification, due diligence, onboarding, oversight, and exit across the thirdparty lifecycle. Monitor audit, inspection trends and metrics; identify process, program, and vendor risks; develop predictive analytics to proactively identify emerging risks and drive continuous improvement. Champion and embed Quality by Design principles across clinical thirdparty engagements. Provide strategic leadership for vendor quality oversight, ensuring independence, objectivity, and alignment with regulatory expectations. Partner [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Berlin
[. .. ] human voice to detect heart failure worsening earlier than ever before. Our vision? To extend the lives of people with cardiac conditions and improve their quality of [...]
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[...] life. Tasks As Clinical Trial Operations Manager, you will take operational leadership of our FDA clearance trial for Noah Labs Vox and oversee execution of multiple ongoing EU and US clinical studies. You will work closely with clinical investigators, CRO partners, medical team, product, and data science teams to ensure studies meet regulatory, scientific, and [. .. ] development. Engage with principal investigators and KOLs, fostering long-term academic and clinical partnerships with leading institutions around the world. Ensure audit readiness and proactive risk management across all studies. Monitor study progress and budgets, prepare executive reports, and communicate risks and mitigation strategies to leadership. Contribute to scientific dissemination, including abstracts, publications, and conference presentations. Requirements Required Qualifications Bachelors degree or higher in Life Sciences, Medicine, Biomedical Engineering, or a related field 5+ years of experience in clinical research with [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Strategic Partnerships Manager-Germany
• Berlin
About Massive Bio Massive Bio is a rapidly growing healthtech startup founded in 2015 to provide every cancer patient with access to
clinical trials regardless of location or financial [...]
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[...] situation. Our proprietary AIdriven patient recruitment and enrollment platform for oncology clinical trials eliminates traditional enrollment barriers and accelerates lifesaving research. Privately held and headquartered in Boca Raton, FL, with operations across multiple countries, our passionate team is transforming how clinical trials connect with [. .. ] additional services and identifying new collaboration opportunities; conduct regular business reviews with partners to optimize performance and identify growth areas. Crossfunctional Collaboration Partner with Clinical Operations team to ensure seamless trial launches and execution; collaborate with Product and Technology teams to incorporate partner feedback and requirements; work closely with Business Development team on lead qualification and opportunity development; support Marketing team with partnership announcements, case studies, and thought leadership content. Market Intelligence Strategy Monitor competitive landscape and partnership trends in German clinical trials market; provide market insights and partnership intelligence to inform business strategy and product development; track partnership performance metrics and ROI to optimize collaboration models; identify emerging opportunities in oncology research and pharmaceutical development. Ideal Candidate Profile Essential Experience 35 years in [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
Jobticket
Associate Director Regulatory Affairs
Clinical Lead page is loaded # # Associate Director Regulatory Affairs Clinical Lead locations: Munich: Tuebingen (Germany) : Remote Work (Germany) time type: Full timeposted [...]
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[...] on: Posted Todayjob requisition id: JR100644OVERVIEWWe are currently seeking an Associate Director Regulatory Affairs Clinical Lead to strengthen our EU Regulatory team. In this role, you [. .. ] compliance with regulatory requirements Lead the preparation and coordination of Scientific Advice and other Health Authority interactions, including briefing documents, responses to questions, and meeting follow-up. Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications. Identify regulatory risks early and propose pragmatic mitigation strategies. Monitor the regulatory landscape, evaluate and translate evolving EU regulatory requirements (including ATMP framework) into strategic implications for development programs. Ensure high-quality, coherent regulatory documentation aligned with overall development strategy and compliant with applicable regulatory regulations and guidelines. Actively support cross-functional alignment to avoid late-stage regulatory issues and [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Senior Scientist (f/m/d) - Immunomonitoring
• Martinsried, Bayern
[. .. ] Would you like to be part of a newly formed and highly motivated and skilled Immunomonitoring team dedicated to developing and implementing (bio) analytical assays and using [...]
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[...] these assays for clinical sample analysis to monitor immune responses induced by Bavarian Nordics innovative new vaccine candidates? Then we are looking for you At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that unlock the immune systems power. We are a global leader in smallpox and mpox vaccines with a portfolio that [. .. ] with automated liquid handling systems. You work independently, are a team player, communicate well, and thrive in a global organization. Your Role Daily management of vaccine immunogenicity testing using clinical trial samples, including assay monitoring, troubleshooting and CRO oversight of offsite sample storage and shipments. Method development, optimisation and validation as required, in compliance with international guidelines. Responsible for automating platebased assays using liquid handlers (e. g. Biomek i7) . Maintain and improve GCLP quality standards, preparing and reviewing technical and [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
• Genf
Führungs-/ Leitungspositionen
The Senior Director,
Clinical Project Management will provide strategic leadership in the planning, execution, and oversight of clinical programs, with a particular focus on designing clinical development plan inputs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and tracking progress against the Target Product Profile (TPP) . This role will ensure the alignment of program activities with regulatory, business, and scientific objectives, [. .. ] ideal candidate combines deep clinical project management experience with strong scientific and strategic insight to support study design and program execution. Key Responsibilities Lead crossfunctional teams to develop, implement, and monitor clinical development plans, ensuring alignment with the Target Product Profile and regulatory strategy. Provide strategic input into study design, protocol development, and endpoint selection to optimize program success. Track, report, and communicate program progress against the TPP, clinical development milestones, and regulatory timelines. Oversee selection, management, and performance of CROs [. .. ] in designing clinical development plans, defining endpoints, and supporting study design. Proven experience in managing CROs and vendors, with strong negotiation and oversight capabilities. Deep understanding of regulatory requirements, clinical trial operations, and therapeutic development. Strong leadership, communication, and stakeholder management skills. Ability to synthesize complex scientific and operational data into actionable insights for executive leadership. Email (please attach CV) : About Planet Pharma Planet Pharma is an American parented Employment Business/ Agency that provides global staffing services with its headquarters [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Director Regulatory Affairs Oncology (m/f/d)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] partners, CROs) , providing expertise for regulatory strategy to achieve regional and global company goals. Roles and Responsibilities Act as European regulatory lead supporting assigned projects in [...]
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[...] different stages of clinical development (early Phase 1-Phase 3) covering product development plans, clinical trial and marketing authorization applications (MAA) as well as product life cycle management. Develop and lead regulatory strategies for drugs and biologics, including orphan drug designation (ODD) , paediatric development plans (PIP) , clinical trial applications, submission dossiers for MAAs, and interactions with national European Health Authorities and EMA. Represent European [. .. ] regulatory roadmaps, document and dossier reviews, coordination with Health Authorities, and supervision of regulatory service providers. Act as regulatory contact person for national Health Authorities and EMA for assigned projects. Monitor changes and evolution in the regulatory landscape for relevant products and product classes, new regulations impacting assigned projects and communicating to relevant stakeholders. Education Experience University degree in life sciences (medicine, pharmacy, chemistry, biotechnology, biology or equivalent) , Master and/or Ph D preferred Master Degree in Regulatory Affairs is a [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
• Zürich
Rivia is a data engine for
clinical trial intelligence. It provides data infrastructure and AI-driven workflows for clinical trial teams, enabling biotechs to run studies more efficiently and to demonstrate [...]
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[...] which patients derive the greatest benefit from new therapies. Biopharma companies are the source of most therapeutic innovation, yet clinical development is frequently slowed by fragmented data [. .. ] platform for clinical trial intelligence. The Role As a Senior AI Engineer at Rivia, you will architect and ship high-impact AI workflows that materially improve how clinical trial teams monitor studies, assess data quality, and make operational decisions. You will work as a key technical contributor embedded in product initiatives, owning AI features end-to-end from design and evaluation through to deployment, observability, and continuous improvement. The ideal candidate is a product-minded engineer who combines deep LLM and [. .. ]
Job am 19.02.2026 bei Jobleads gefunden
(Associate) Director, Clinical Research Scientist
Führungs-/ Leitungspositionen
Position Overview This position supports the scientific planning and execution of one or more
clinical trials or significant aspects thereof. In this position, you will have the opportunity to [...]
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[...] demonstrate your technical skills, and scientific acumen as part of a global, cross-functional team. Responsible for leading specific aspects of clinical/ scientific execution of clinical protocol (s) . Responsibilities Serve as clinical scientist on the clinical trial team Support the medical monitoring team in review and interpretation of clinical data and medical protocol deviations Provide data review per Data Review Guideline to ensure high-quality data of the study on an ongoing basis Collaborate cross-functionally in the development of study protocol and related study materials (e. [. .. ] Ensure CRF design supports data collection in alignment with the protocol in collaboration with Data Management/ Programming Support site initiation activities and interactions with site staff Collaborate cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct Support investigator meeting (s) , IDMC meeting (s) and thought leader interactions Qualifications Degree in life sciences (such as medicine, pharmacy, biology) with at least 5-years experience in clinical research/ development required. Advanced degree (MD, Ph D, Pharm D or [. .. ]
Job am 13.02.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] and guidance to ensure pipeline assets meet future market access needs and maximize commercial potential. The person in this position will focus on identifying market access-related evidentiary [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] gaps in clinical development plans that could result in a breadth of reimbursement inconsistent with planned labelled population (s) and/or pricing that does not sustainably support the business. The person in this role will work cross-functionally with relevant stakeholders to develop recommendations to close those gaps and/or for evidence generation [. .. ] pipeline products (typically but not exclusively Phase II and III assets) , aligning with clinical and commercial goals. Collaborate cross-functionally to integrate access requirements into the development process, influencing trial design, endpoints, and evidence generation to meet payer needs. Lead the collection and aggregation of feedback from all regions in which the Company operates and develop recommendations regarding clinical development and other evidence generation based on that feedback. In alignment with the ED, GVAP ST, represent the GVAP ST perspective [. .. ] them to engage with payers as the product nears market entry. Support regional activities relating to regional asset in-licensing for early pipeline products. Market Insights Competitive Landscape Analysis: Continuously monitor the solid tumor landscape, including competitor activities, evolving payer requirements, and regulatory changes that impact access and reimbursement. Run analysis of payer insights, pricing trends, and market conditions to inform strategy adjustments and refine access plans. Use global and regional insights to refine value propositions and enhance product positioning as [. .. ]
Job am 12.02.2026 bei Jobleads gefunden
Study Physician sponsor dedicated in Germany
• München, Bayern
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Job Responsibilities Study Physician Medical Doctors (Candidates who completed fellowship, residency, specialization e. g. Internal medicine, oncology, neurology, immuneoncology, cardiology, pediatrics, emergency medicine are preferred) with following experience:-Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. -Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. -Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company. -Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in [. .. ]
Job am 03.02.2026 bei Jobleads gefunden
Regulatory Affairs Executive
• Verna, Hessen
[. .. ] and a minimum of 2 to 5 years of experience. Roles and Responsibilities Develop and implement regulatory strategies to ensure compliance with industry regulations. Prepare and review [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory documents, including clinical trial applications and marketing authorizations. Collaborate with cross-functional teams to ensure timely submission of regulatory documents. Monitor and analyze changes in regulatory requirements and develop plans to implement updates. Provide training and guidance to internal stakeholders on regulatory requirements. Ensure accurate and timely tracking of regulatory submissions and correspondence. Job Requirements Bachelors degree in Life Sciences or a related field. Minimum 2 to 5 years of experience [. .. ]
Job am 27.01.2026 bei Jobleads gefunden
Business Development Manager Be NeLux/ Scandinavia
• München, Bayern
Conscio Group, offers fully integrated services across the entire lifecycle of pharmaceutical products. Our network of sites across Europe offers comprehensive capabilities in formulation development,
clinical trial material (IMP) manufacturing, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical studies, bioanalytical testing and quality control services. Due to our rapid growth across Europe, we are now hiring a Business Development Manager Be Ne Lux/ Scandinavia Key Responsibilities Identify and develop new business opportunities within the pharmaceutical sector in the Be Ne Lux and Scandinavia region. Build and [. .. ] scientific and technical teams to tailor solutions for client needs. Represent Conscio Group at industry events, conferences, and networking opportunities. Prepare and deliver presentations, proposals, and reports to prospective clients. Monitor market trends, competitor activities, and regulatory changes relevant to the pharmaceutical industry. Requirements Educational Background: Advanced degree (MSc or Ph D preferred) in Pharmaceutical Sciences (preferred) , Chemistry, Pharmacology, or a related scientific field. Professional Experience: 2-5 years hands-on experience in pharmaceutical development (R D, formulation, analytical development, project [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
Software Engineer
• Estenfeld (VGem) , Bayern Estenfeld (VGem)
Work-Life-Balance
[. .. ] Engineer II (f/m/d) at our Clario site in Estenfeld (near Würzburg) for developing and successfully delivering a project-specific highly-interactive mobile-web and other software applications for
clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] research data acquisition and data management that is deployed onto worldwide distributed Smartphones, Tablets and Asthma monitor devices. Become a part of driving clinical studies forward with your daily performance with us. You will be responsible for ensuring that our customers (pharmaceutical companies, Bio Techs, and CROs) receive software applications according to the study specifications. Even if you dont have experience in the world of clinical trials, [. .. ] and collaborate on technical questions. Work collaboratively within an international team of Software Development Engineers, supporting projects and addressing technical questions. Develop, deploy, and maintain software applications based on clinical trial software specifications. Integrate acquired device data with backend project-specific databases. Participate in decision-making throughout the development life cycle of clinical trial study data collection applications. Contribute to project specification development and the planning and deployment scheduling process. Review moderate to high-complexity code from other engineers and write [. .. ]
Job am 21.12.2025 bei Jobleads gefunden
Senior Data Scientist II-Therapeutic Modality Insights Competitor Intelligence (all genders)
• Ludwigshafen am Rhein, Rheinland- Pfalz
[. .. ] knowledge and insights mining and analysis, as well as designing and building innovative selfservice solutions for insights generation from published resources and internal knowledge. This includes literature, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing Abb Vies competitiveness by driving Therapeutic Modality Knowledge Intelligence Solutions. You will lead the creation of [. .. ] agentic workflows) that address significant scientific and strategic trends and knowledge gaps in therapeutic modalities. Develop and deliver innovative, highquality intelligence solutions that systematically extract, analyze, summarize, integrate and proactively monitor key knowledge about novel therapeutic modalities (such as gene/ cell therapies and innovative RNA or antibodybased drugs) to address urgent scientific and business needs. Apply broad expertise in knowledge information science, Generative AI/ NLP, data warehousing, and software development to build robust data pipelines and analytical workflows for large and [. .. ]
Job am 19.12.2025 bei Jobleads gefunden
Senior Data Scientist II Therapeutic Modality Insights Competitor Intelligence (all genders)
• Ludwigshafen am Rhein, Rheinland- Pfalz
Work-Life-Balance
[. .. ] knowledge and insights mining and analysis, as well as designing and building innovative selfservice solutions for insights generation from published resources and internal knowledge. This includes literature, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing Abb Vies competitiveness by driving Therapeutic Modality Knowledge Intelligence Solutions. You will lead the creation of [. .. ] workflows) that address significant scientific and strategic trends and knowledge gaps in therapeutic modalities. Develop and deliver innovative, high-quality intelligence solutions that systematically extract, analyze, summarize, integrate and proactively monitor key knowledge about novel therapeutic modalities (such as gene/ cell therapies and innovative RNA or antibody-based drugs) to address urgent scientific and business needs. Apply broad expertise in knowledge information science, Generative AI/ NLP, data warehousing, and software development to build robust data pipelines and analytical workflows for large [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical trial monitor pro Jahr?
Als Clinical trial monitor verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Monitor Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 45 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Jobs?
Aktuell suchen 18 Unternehmen nach Bewerbern für Clinical Trial Monitor Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Monitor Stellenangebote:
- Greiner (2 Jobs)
- NEVEON Executive Committee (2 Jobs)
- Avomind (2 Jobs)
- IQVIA (2 Jobs)
- Noah Labs (2 Jobs)
- Abb Vie (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Monitor Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Monitor Jobs werden derzeit in Bayern (10 Jobs), Berlin (8 Jobs) und Hessen (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
