5 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job vor 4 Tagen bei Mindmatch.ai gefunden
Biogen, Inc.
• 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 vor 4 Tagen bei Mindmatch.ai gefunden
Biogen, Inc.
• 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 [. .. ]
Job am 24.07.2026 bei Mindmatch.ai gefunden
Novocure Inc.
• AT- 2 Schweiz
Select how often (in days) to receive an alert: Create Alert At Novocure, every role contributes to extending the lives of people living with cancer. As our new Manager, Global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Supply Chain, youll play a key role in ensuring our clinical studies have the right investigational product available at the right place and the right time-supporting patients and clinical teams around the world. This is a highly autonomous, end-to-end operational role reporting to the Director, Global Clinical [. .. ] the endtoend clinical supply process, from demand forecasting through manufacturing, packaging, distribution and site delivery. Develop and manage studylevel demand forecasts, inventory strategies and resupply plans to ensure uninterrupted clinical trial supply. Coordinate drug orders with pharmaceutical partners and secure manufacturing capacity with external suppliers. Lead packaging and labelling activities while overseeing depots, storage, transportation, returns and product destruction. Partner closely with Clinical Operations, Quality, external manufacturers, CROs and logistics providers to ensure successful study execution. Monitor supply risks including expiry, shortages, recalls and distribution challenges, proactively identifying and implementing mitigation plans. Coordinate customs documentation and shipment activities to support global clinical trial execution. Maintain supply documentation, study trackers and TMF readiness while ensuring highquality operational documentation. Serve as the primary operational supply contact for assigned studies, [. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] activation through to study closure at country and site level in accordance with the Monitoring Plans. Reviews monitoring visit reports (as required and following Sponsor SOPs) and proactively advises the monitor (s) on study related matters. Performs any required comonitoring, Accompanied Site Visits/ training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organises regular Local Study Team meetings on an agenda driven basis. Actively works towards achieving good personal relationships with all Local [. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] activation through to study closure at country and site level in accordance with the Monitoring Plans. Reviews monitoring visit reports (as required and following Sponsor SOPs) and proactively advises the monitor (s) on study related matters. Performs any required comonitoring, Accompanied Site Visits/ training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organises regular Local Study Team meetings on an agenda driven basis. Actively works towards achieving good personal relationships with all Local [. .. ]
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 5 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Monitor Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Monitor Jobs werden derzeit in Schleswig-Holstein (0 Jobs), Thüringen (0 Jobs) und Berlin (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
