54 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job gestern bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
• Munich, BY Muenchen
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more countries/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job gestern bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Essen, NW
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more countries/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job gestern bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Stuttgart, BW
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more countries/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Berlin, BE
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more countries/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Düsseldorf, NW Duesseldorf
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more countries/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Leipzig, SN
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] countries/ regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Dortmund, NW
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] countries/ regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Hamburg, HH
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] countries/ regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Clinical Trial Liaison, Oncology
• Frankfurt
Territory includes: Austria, Germany, Switzerland The
Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] countries/ regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country specific insights [. .. ] Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts Attend and present at investigator meetings, monitor workshops/ training Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e. g. feasibility, startup activities, enrolment or escalated study/ site issues Responsible for review, documentation and follow up of investigator site issues [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
SCIRENT Clinical Research and Science
Clinical Project Manager
• Brandenburg
SCIRENT
Clinical Research and Science is seeking a dedicated Clinical Project Manager for a full-time position in Germany. As a Clinical Project Manager, you will be responsible for the planning, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] coordination, and execution of clinical trials in the cardiovascular field. You will be the primary point of contact for internal teams, [. .. ] departments, maintaining a focus on clinical objectives. Quality and Compliance: Ensure high-quality execution of studies, adherence to timelines, budgets, and strict compliance with regulatory requirements. Risk and Progress Management: Monitor study progress, manage risks, initiate corrective actions, and lead escalation processes where necessary. Audit Readiness: Prepare for and support audits and inspections, ensuring full regulatory compliance throughout the study lifecycle. Budget and Documentation Oversight: Supervise study budgets, contractual obligations, and maintenance of essential study documentation. Your Profile Education: Bachelors degree [. .. ] therapies for cardiac patients. What sets us apart from our competitors is our profound expertise in cardiovascular therapy and diagnostics. Our CRO offers access to an impeccable network of dedicated trial centers in Europe and North America with extensive experience in cardiovascular studies. Our customers appreciate our lean and agile management, which generally makes our performance faster and more efficient. We look forward to receiving your complete application documents, including the proposed start date of work. CEO: Prof. Dr. med. Hans-[. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Rivia
• AT- 2 Lavamünd
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 3 Tagen bei Mindmatch.ai gefunden
ALTEN
Senior HEOR Manager-Hematology Europe and new markets
• AT- 2 Lavamünd
[. .. ] the expansion and optimization of our hematology portfolio across Europe and emerging markets. In this role, you will develop and execute a comprehensive HTA (Health Technology Assessment) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and JCA (Joint Clinical Assessment) strategy to ensure timely market access, reimbursement, and adoption of our innovative hematology therapies. You will work closely with cross-functional teams (Medical, Regulatory, Commercial, and Government Affairs) to align evidence generation, pricing, and market access strategies with the evolving European HTA/ JCA landscape. Your expertise will be critical [. .. ] Key Responsibilities: Lead the development and implementation of a pan-European HTA/ JCA strategy for the hematology portfolio, ensuring alignment with EU regulations (HTA Regulation 2021/ 2282) and national requirements. Monitor and analyze the evolving JCA process (Joint Clinical Assessment) for hematology products, including oncology and rare blood disorders, and adapt strategies accordingly. Coordinate with EU and national HTA bodies (e. g. , EUnet HTA, HAS, NICE, IQWi G, AIFA) to anticipate evidence requirements and optimize submission dossiers. Identify and mitigate risks related [. .. ] to support HTA/ JCA submissions. Develop compelling value propositions tailored to payors, clinicians, and HTA committees, highlighting clinical efficacy, safety, and economic benefits of hematology therapies Ensure alignment between clinical trial data, real-world evidence (RWE) , and pharmacoeconomic models to meet HTA/ JCA standards. Market Access Reimbursement Lead pricing and reimbursement (P R) strategies for hematology products, including negotiations with payors, managed entry agreements (MEAs) , and risk-sharing schemes. Support country-specific market access plans by providing strategic guidance [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
The IQVIA
Clinical Functional Service Partnerships (Clinical FSP) department provides highly skilled professionals who work as integrated members of our clients clinical development teams. In this role, you will combine [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] operational depth with strategic and scientific leadership, while being supported by experienced functional experts, technology, and data-driven insights. We are looking for a (Senior) Clinical Trial Leader who can take clear accountability for complex global Phase III trials, lead cross-functional teams, and turn scientific ambition into successful trial delivery. Lead with purpose. Shape the strategy. Deliver globally. (Senior) Global Clinical Trial Leader This opportunity is especially suited to you if you: currently lead, or have [. .. ] GCP, ICH, applicable global and local regulations, sponsor procedures, and inspection-ready documentation throughout the trial lifecycle. Use data to steer performance: Use dashboards, metrics, systems, and operational reviews to monitor progress, identify trends, ensure timely data cleaning and delivery, and protect milestone achievement. Support critical trial outputs: Coordinate cross-functional contributions to core trial and patient-facing documents, amendments, training updates, authority and ethics responses, safety and data monitoring activities, clinical trial reporting, TMF completeness, registry disclosure, and publication support [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Rivia
Customer Engagement Manager
• AT- 2 Lavamünd
About Rivia 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and to demonstrate 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 [. .. ] they are successfully met through Rivias platform. Develop and execute customer engagement plans to drive client engagement, satisfaction, and retention. Conduct regular check-ins and business reviews with clients to monitor progress and identify opportunities for optimization. Provide proactive support and guidance to clients, addressing any issues or concerns promptly and effectively. Collaborate with the sales, product, and technical teams to ensure a seamless customer experience, optimize product and go-to-market strategies. Educate clients on new functionalities of the Rivia [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Rivia
• AT- 2 Lavamünd
About Rivia Rivia is a technology company building a data engine that powers the future of
clinical trial intelligence. Rivia was founded on the belief that new drugs can [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] be brought to market more successfully with a fraction of todays capital. Biotechs are the source of most therapeutic innovation, yet clinical development is constantly constrained by fragmented data and outdated tooling. Rivia unifies clinical trial data at scale [. .. ] 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 vor 5 Tagen bei Mindmatch.ai gefunden
MSD
Specialist Upstream Operations (m/f/d)
• AT- 2 Lavamünd
[. .. ] they belong at Schachen, but that the site belongs to and is shaped by them. Our Schachen Biotech is a premier, stateoftheart facility that integrates advanced technologies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] into the earlystage clinical pipeline, refining them for future commercial launch. The site supports biologics drug substance manufacturing for earlyphase clinical supply and serves as a hub for technology innovation and strategic advancement. The Specialist Upstream Operations position requires fulltime physical presence at the site to support manufacturing and to enable optimal integration into [. .. ] to our employees and the community around us. Our Werthenstein Bio Pharma site in Schachen is where we conduct cuttingedge research, develop and analyze new biological agents and supply clinical trial products for global clinical studies. The site is also home to one of our global forensic laboratories where we carefully monitor our products through the supply chain to ensure security and safety for our patients. Required Skills Accountability Accountability Adaptability Business Agility Competency Management Contract Manufacturing Data Analysis Deviation Management Engineering Management Engineering Standards Knowledge Sharing Leadership Training and Development Manufacturing Manufacturing Documentation Manufacturing Processes Manufacturing Quality Control Manufacturing Scale Up [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
• AT- 2 Lavamünd
[. .. ] aos cuidados de sade hoje e nas geraes futuras. Junte-se Roche, onde cada voz importante. # # # A posio As part of the Production Enablement team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] within Global Clinical Supply Chain Management, you will join a collaborative and global network dedicated to ensuring clinical packaging operations run seamlessly and on time. In this dynamic role as Global Clinical Artwork Manager, you will serve as the pivotal link between cross-functional teams, external partners, and regulatory networks to design and [. .. ] extension labels. Collaborate cross-functionally with Clinical Study Planning, global manufacturing teams, external suppliers, and a worldwide network of regulatory label representatives. Drive issue resolution in the label creation process, monitor labeling regulations, and maintain critical master data and documentation. Lead supplier relationship management and performance reviews with external booklet vendors to drive continuous improvement. Support emerging packaging technologies by coordinating the development and testing of new label capabilities with external vendors. Champion label-related operations for pre-approval access and post-trial access programs to support global patient needs. # # # # # # Who You Are Education: University degree in Pharmaceutical Sciences, Biopharmaceuticals, Supply Chain Management, or a related field. Experienced professional with 3+ years in the pharmaceutical, biopharmaceutical, or clinical supply chain environment. Knowledgeable in pharma supply [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
NVIDIA
Senior Developer Relations Manager-Agentic Healthcare AI
• AT- 2 Lavamünd
[. .. ] Advise on the technical enablement resources-such as sample code, guides, demonstration pipelines, and tools to highlight the application of technologies in solving real-world problems, i ncluding scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reasoning, clinical development of pharmaceutical products (e. g. , trial matching, regulatory submissions) , ambient clinical documentation, cross specialty agent orchestration etc. Guide customers, partners, and startups through onboarding and integration with NVIDIAs programs, fostering co-innovation and the development of next-generation solutions. Map, track, and monitor the European healthcare and life sciences ecosystem, particularly around agentic AI, to identify growth opportunities, inform technology roadmaps, and shape adoption strategies. Collaborate multi-functionally with solution architects, engineering, product management, and marketing to drive developer engagement and optimize partner adoption strategies. Engage with partner engineering teams, technical leaders, and [. .. ]
Job vor 9 Tagen bei Mindmatch.ai gefunden
Future Meds GmbH
• AT- 4 Braunau am Inn
Flexible Arbeitszeiten
[. .. ] von morgen beizutragen und klinische Studien kennenzulernen. Dies ist auch eine Chance, neben Ihrer Vollzeitbeschäftigung oder in einer arbeitsfreien Zeit neue Fähigkeiten zu erwerben. Ihr Future Meds-Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] English below: Clinical Research Nurse for Homecare visits Future Meds is a service provider working with clinical study sites to deliver home-based care for patients participating in clinical studies. We are based in Berlin, Germany and are linked to study sites in various countries in Europe including the Austria. Future Meds offers [. .. ] nurse in the area of Vienna for a weekly and monthly visit. The first planned visit would probably be February/ March. Responsibilities: Assessments of changes in the patients well being Monitor changes in the patients concomitant medication Review of medication diary Blood collection, processing, packaging and shipping according to applicable guidelines Processing of urine samples Completion of Source Document Requirements: Nurse diploma At least 2 years of practice nice to have Experience with phlebotomy-nice to have Why should you apply: You will receive a paid training on the protocol of the clinical trial by web conference or by telephone All the necessary equipment to carry out the home visit will be provided by us You will be contracted to work for Emovis directly and paid for the performed visits We are interested in a long term cooperation. If we are satisfied with one [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Gouya Insights
Clinical Project Manager
• AT- 9 Wien
Looking for an opportunity to put your
clinical project management skills to the test? We are seeking an experienced Clinical Project Manager to join our team at Gouya Insights [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gmb H Co KG, a clinical development consulting and clinical research services company supporting innovative biotech, pharmaceutical, and medical device companies. As Clinical Project Manager, you will take operational ownership [. .. ] proactive leader who enjoys taking ownership, working in a dynamic early-development environment, and solving the operational challenges that arise when multiple partners need to work together. Key Responsibilities Clinical Trial Management Lead the operational delivery of assigned clinical studies from planning and start-up through study execution, database lock, and close-out. Develop and manage study plans, timelines, budgets, deliverables, and risk-mitigation activities. Lead regulatory activities to ensure timely approvals and keep site activation on schedule. Coordinate site feasibility, [. .. ] Review scopes of work, proposals, budgets, assumptions, invoices, and change orders and identify potential gaps or budget risks. Ensure clear responsibilities, interfaces, timelines, deliverables, and escalation pathways across external partners. Monitor CRO and vendor performance against agreed scope, quality, timelines, and budgets. Manage interfaces and dependencies between vendors, ensuring that outsourced activities remain appropriately controlled and aligned with sponsor oversight responsibilities. c. Client Stakeholder Management Act as a key operational contact for assigned clients, providing transparent reporting on project status, timelines, [. .. ]
Job am 07.08.2026 bei Mindmatch.ai gefunden
Biogen, Inc.
Regional Study Start-Up Lead
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] efforts, communicating strategies to country teams, and monitoring progress to maintain alignment with business goals. By spearheading these initiatives, you contribute significantly to our overarching mission of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] delivering high-quality clinical trials and advancing healthcare solutions. What Youll Do: Lead day-to-day management of multiple projects or a multi-study program for site activation. Drive site selection processes within your region to ensure timely and efficient activation. Oversee site activation according to timelines and quality standards across a region. Communicate site activation strategy to country teams and monitor progress. Act as a SME in EUCTR ensuring timely collection of part 2 documents for all countries and sites that you are overseeing. Ensure that all ECs and Regulatory authorities have been paid in an appropriate timeframe Coordinate SSU specialists across regions and ensure all sites within regions are on [. .. ] ensuring that priorities are met in a timely manner. Required Skills: Bachelors Degree in life sciences or equivalent (e. g. , pharmacy, nursing) . Minimum of 8 years of clinical trial experience, with at least 5 years in a study start-up role and at least 3 at a regional level. Previous experience in a Contract Research Organization (CRO) is essential. Strong EUCTR experience previously involved in submissions. Experience of start up in APAC region Proven experience in project management and [. .. ]
Job am 07.08.2026 bei Mindmatch.ai gefunden
Biogen, Inc.
Associate Director, Country Site Operations FSP Oversight Manager
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] leadership and cross-functional stakeholders to drive and manage the CSOs FSP insourcing model. This role is crucial in overseeing and developing FSP staff who support country-and site-facing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical trial execution, ensuring the embedding of consistent, efficient processes across regions and therapeutic areas. Your work will ensure alignment with CSOs internal and external stakeholders on FSP role execution, performance, quality, and delivery expectations. Additionally, you will contribute to shaping CSO operational strategy and continuous improvement as part of the CSO [. .. ] and offboarding of FSP resources, ensuring smooth transitions, role clarity, policy compliance, and continuity of country and site support. Represent CSO in FSP vendor governance, oversight, and performance management forums. Monitor, analyze, and report applicable FSP role performance metrics, quality indicators, workload trends, and delivery risks. Partner with CSO regional leaders, study teams, Medical, Quality, and other stakeholders to align on goals, strengthen site-centric execution, and promote continuous improvement. Who You Are: You are an experienced professional in clinical research [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Director of Veterinary Clinical Trials Operations
• Zürich Zuerich
Führungs-/ Leitungspositionen
The University Animal Hospital Zurich invites a highly organized veterinarian to establish and lead
clinical trial operations under Gx P. You will plan, coordinate and deliver academic and industry-sponsored [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trials, collaborating with researchers, clinical teams and external partners to ensure compliant, high-quality study conduct. You will manage the trial portfolio, monitor milestones, and drive continuous improvement of processes and quality systems. #J-18808-Ljbffr 03740671 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Senior AI Engineer: Agentic AI for Clinical Trials (Zurich)
• Lavamünd, Kärnten Lavamuend
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 3 Tagen bei Jobleads gefunden
Senior HEOR Manager-Hematology Europe and new markets
• Lavamünd, Kärnten Lavamuend
[. .. ] the expansion and optimization of our hematology portfolio across Europe and emerging markets. In this role, you will develop and execute a comprehensive HTA (Health Technology Assessment) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and JCA (Joint Clinical Assessment) strategy to ensure timely market access, reimbursement, and adoption of our innovative hematology therapies. You will work closely with cross-functional teams (Medical, Regulatory, Commercial, and Government Affairs) to align evidence generation, pricing, and market access strategies with the evolving European HTA/ JCA landscape. Your expertise will be critical [. .. ] Key Responsibilities: Lead the development and implementation of a pan-European HTA/ JCA strategy for the hematology portfolio, ensuring alignment with EU regulations (HTA Regulation 2021/ 2282) and national requirements. Monitor and analyze the evolving JCA process (Joint Clinical Assessment) for hematology products, including oncology and rare blood disorders, and adapt strategies accordingly. Coordinate with EU and national HTA bodies (e. g. , EUnet HTA, HAS, NICE, IQWi G, AIFA) to anticipate evidence requirements and optimize submission dossiers. Identify and mitigate risks related [. .. ] to support HTA/ JCA submissions. Develop compelling value propositions tailored to payors, clinicians, and HTA committees, highlighting clinical efficacy, safety, and economic benefits of hematology therapies Ensure alignment between clinical trial data, real-world evidence (RWE) , and pharmacoeconomic models to meet HTA/ JCA standards. Market Access Reimbursement Lead pricing and reimbursement (P R) strategies for hematology products, including negotiations with payors, managed entry agreements (MEAs) , and risk-sharing schemes. Support country-specific market access plans by providing strategic guidance [. .. ]
1 von 3Weiter » Weitere Suchergebnisse laden »
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 54 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Jobs?
Aktuell suchen 12 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:
- Rivia (3 Jobs)
- SCIRENT Clinical Research and Science (2 Jobs)
- ALTEN (1 Job)
- IQVIA (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Monitor Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Monitor Jobs werden derzeit in Bayern (4 Jobs), Niedersachsen (4 Jobs) und Nordrhein-Westfalen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
