86 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job gestern bei Jooble gefunden
• München
Study Physician sponsor dedicated in 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Responsibilities Study Physician Medical Doctors (Candidates who completed fellowship, residency, specialization e. g. Internal medicine, oncology, neurology, immune-oncology, 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 vor 10 Tagen bei Jooble gefunden
Abb Vie
Senior Data Scientist II-Therapeutic Modality Insights Competitor Intelligence (all genders)
• Ludwigshafen am Rhein
Work-Life-Balance
[. .. ] and insights mining and analysis, as well as designing and building innovative self-service solutions for insights generation from published resources and internal knowledge. This includes literature, patent, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
• Karlsruhe
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, [. .. ] day in the Life: Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools Reviews regulatory documents for proper content Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments Assists with the identification of potential investigators and development/ distribution of initial protocol packets May assist the project team with the [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Clinical Research Associate (Klinischer Monitor)
• Homeoffice
[. .. ] scale. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success. PPDs Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice
[. .. ] scale. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success. PPDs Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• Homeoffice
[. .. ] scale. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success. PPDs Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
• München
Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stronger study delivery. Job Description As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities [. .. ] leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. This is a regional role, with the region to be assigned. Key Responsibilities Take end-to-end operational responsibility for clinical research projects within the assigned region. Ensure effective execution of clinical trials in [. .. ] for coordinators facing operational challenges. Proactively manage risks, troubleshoot operational bottlenecks, and lead local resolution Collaborate closely with internal global teams to ensure alignment, clear communication, and seamless project execution. Monitor operational KPIs, prepare progress reports, and implement corrective actions where needed. Represent Milestone One in operational discussions with sponsors, partners, and at selected industry meetings. Qualifications Minimum 5 years of experience in leadingclinical trial operations within an SMO or CRO Proven hands-on experience in managing clinical trial operations, including site [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Avomind
(Senior) Clinical Research Scientist-Digital Cardiology and Heart Failure
• Berlin
[. .. ] pioneering a new era of digital cardiology. Their flagship technology applies machine learning to the human voice to detect heart-failure worsening earlier than any existing method, transforming [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] how clinicians monitor and manage their patients. Building on a strong foundation of international clinical trials, they are now entering the next chapter: bringing this breakthrough technology to market and expanding the clinical evidence base to establish their technology as the new standard of care. Together with their deployed remote monitoring platform, which is already trusted by more than 200 cardiologists and more than 1, [. .. ] This is not a back office research role. You will be at the center of our mission, connecting clinical research, scientific development, and medical affairs. The position combines hands-on trial execution with high-level strategic and cutting-edge scientific work in a fast-moving start-up environment. Working closely with their Chief Medical Officer and the R D Team, you will help shape their global evidence strategy across pivotal trials, AI validation, and real-world studies. You will collaborate directly [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Ascendis Pharma
• Heidelberg
Are you passionate aboutclinical disclosure and transparency? Do you have experiencewithinthe field? If so, now is your chance to join Ascendis Pharma as our new
Clinical Disclosure Specialist. Ascendis [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Pharmais a global biopharmaceutical company committed to making a meaningful difference in patients lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative Trans Con technology platform to fulfill our mission of developing new therapies thatdemonstratebest-in-class potential to address [. .. ] working together to achieve extraordinary results. Youwill be joining the Global Regulatory Communicationsteamas the pioneer Clinical Disclosure Specialist in Ascendis, andbebasedin Copenhagen. Your key responsibilities willinclude: Overall responsibility for clinical trial disclosure activities Own CCI management processes Develop and implement relevant processes, including training of colleagues in requirements Monitor and interpret global and future CTD requirements Collaborate cross-functionally with clinical, regulatory, and other teams to meet disclosure requirements. Qualifications and Skills: You hold a relevant degreein a scientific discipline-preferably advance level-withminimum 5years of experience withinbiopharma and minimum 2 years in CTD. Furthermore, you have: Deep knowledge [. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
Clinical Research Associate
• Mainz
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Clinical Research Associate. About this role As part of our FSP team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. This role is dedicated to one of our clients. This role is a full-time role based Germany. Key Responsibilities: Monitor clinical trial sites to ensure protocol, GCP, and regulatory compliance Conduct site visits (initiation, monitoring, and close-out) and prepare visit reports Verify source data and ensure accurate, timely data entry Support site staff with study procedures and documentation Identify, escalate, and help resolve study issues and risks Qualifications: Bachelors degree in [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Chapter 2
• Berlin
[. .. ] and most importantly, to each otherbecause we know that true success is built together. Chapter 2 A scalable talent solution. For more information, please watch the Chapter [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2 Evolution (Senior) Clinical Research Scientist Digital Cardiology Heart Failure Location: Berlin Type of role: Permanent Sector: Digital Health/ Medical Technology (Cardiology AI) Working environment: Office-based with flexibility Breakdown of hybrid arrangement: Hybrid (minimum 3 days in the office) or remote (less preferred) Working days and hours: Monday to Friday, full time Language [. .. ] organisation, connecting clinical research, scientific development, and medical affairs in a fast-paced startup environment, with real influence over both scientific direction and clinical impact. What Youll Do Clinical Research Trial Oversight Oversee sponsor-side clinical operations and budgets across multi-centre studies in Europe and the U. S. Lead, execute, and monitor clinical trials in collaboration with CROs and internal research teams Ensure adherence to GCP and regulatory requirements across all research activities Contribute to protocol design, endpoint definition, and data interpretation alongside R D and data science teams Build and maintain strong relationships with investigators, study sites, and clinical partners Scientific [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Local Clinical Trial Manager-FSP, Germany-6 month FTC (m/f/d)
• Homeoffice
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to [. .. ] processes. Open to travel as needed for the role. Ensures appropriate training of in-country staff and investigator sites; coordinates delivers operational aspects at local study meetings including investigator meetings, monitor meetings, and local training. Escalates resourcing issues to ensure that in-country study activities are appropriately resourced. Ensures robust communication and engagement with sites, e. g. , timely communication of protocol amendments. Reviews and approves Monitoring Visit Reports (MVRs) for their study (s) within agreed timelines to obtain an understanding [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Abb Vie
• Ludwigshafen am Rhein
Work-Life-Balance
[. .. ] challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place Together, we break through as a Data Scientist [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] II for Published Clinical Evidence Competitive Intelligence Insights (all genders) Abb Vies global Information Research (IR) group has a mission to unlock information that makes cures possible. Within IR, the Enterprise Knowledge Accelerator (EKA) team is the trusted knowledge partner for clients in R D and the Corporate Business Strategy Office (CBSO) . EKA [. .. ] insights mining and analysis, as well as designing and building innovative self-service solutions for insights generation from published resources and internal knowledge. This includes literature, patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. The Data Scientist should have sufficiently strong background in both science and technology to fulfil this role and demonstrate high motivation to expand their knowledge in a pharma context and as SME for key client groups. The role is expected to collaborate [. .. ] knowledge extraction from (full-text) publication resources Provide unique scientific insights and expertise by designing and developing solutions for finding, extracting, curating, and visualizing knowledge from published and internal data Monitor and be attuned to new technological trends relevant for knowledge analysis and insights discovery Achieve great results, while demonstrating key Abb Vie values and behaviors. Qualifications This is how you make a difference: Bachelors degree (7+ years of experience) , Masters degree (5+ years of experience) or Ph. D. degree [. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
Study Physician sponsor dedicated in Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Responsibilities Study Physician Medical Doctors (Candidates who completed fellowship, residency, specialization e. g. Internal medicine, oncology, neurology, immune-oncology, 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 22.01.2026 bei Jooble gefunden
PSI CRO
• München
[. .. ] to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description PSI Medical Monitors provide medical input [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to global clinical studies and advise the teams and business partners, while always focusing on patients safety and well-being. Hybrid working based in Munich Responsibilities: Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol [. .. ] annual reports, clinical study reports, patient narratives, and scientific presentations Review and analysis of clinical data to ensure the safety of study participants in clinical trials Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/ amendments Address safety issues across the trial from sites and the study team Provide support for medical data review Participate in bid defense meetings and proposal activities Assist in [. .. ]
Job am 22.01.2026 bei Jooble gefunden
PSI CRO
Clinical Study Monitor
• München
[. .. ] Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. PSI Medical Monitors provide medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] input to global clinical studies and advise the teams and business partners, while always focusing on patients safety and well-being. Hybrid working based in Munich Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and [. .. ] sites, regulatory agencies and third-party vendors on medical matters Review and analysis of clinical data to ensure the safety of study participants in clinical trials Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/ amendments Provide support for medical data review Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines Medical Doctor degree Full working proficiency in English Proficiency with MS [. .. ]
Job am 20.01.2026 bei Jooble gefunden
Catal Ym GmbH
• Planegg
Your mission As (Senior)
Clinical Trial Supply Manager, you will ensure the timely and reliable supply of investigational medicinal products (IMPs) and associated materials to patients participating in our clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trials. You will manage end-to-end clinical supply execution from forecasting and packaging through distribution and returns working closely with CDMOs, Tech Ops, Clinical Operations, [. .. ] IRT system owner for supply chain (study setup, shipments, drug assignment, etc. ) . Vendor CDMO Management Lead day-to-day CDMO project coordination, including regular calls and timeline tracking. Monitor packaging/ labeling progress, batch documentation, release, and distribution. Manage distribution plans, logistics schedules, and timely issue resolution. Define, implement, and maintain SOPs and compliant processes. Drive vendor performance through structured governance and proactive communication. Logistics Distribution Coordinate IMP, QC/ stability sample, and DS-DP transfers and imports worldwide. Serve as [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Hays Professional Solutions GmbH
Clinical Trial Associate für den Bereich Quality Assurance (m/f/d)
• Frankfurt am Main
Angebote von Zeitarbeitsunternehmen
Quality Oversight Systems Management:
Monitor compliance with quality guidelines in
clinical business areas and implement regional quality plans Audit Inspection:Lead and support audit and inspection preparations, including document management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and response coordination Support root cause analysis, CAPA processes, and audit planning Analyze quality metrics to identify gaps and recommend corrective actions to enhance compliance and efficiency Education Experience: Bachelors degree in [. .. ] prioritize and effectively manage multiple tasks Teamwork Flexibility: Independent yet collaborative work style within global teams Experience in a global quality assurance environment and knowledge of regulatory requirements and clinical trial processes German and Englisch fluent Work in an international Company 75796199 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Abb Vie
Data Scientist for Published Clinical Evidence Competitive Intelligence Insights (all genders)
• Ludwigshafen am Rhein
Work-Life-Balance
[. .. ] challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place Together, we break through as a Data Scientist [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] II for Published Clinical Evidence Competitive Intelligence Insights (all genders) Abb Vies global Information Research (IR) group has a mission to unlock information that makes cures possible. Within IR, the Enterprise Knowledge Accelerator (EKA) team is the trusted knowledge partner for clients in R D and the Corporate Business Strategy Office (CBSO) . EKA [. .. ] insights mining and analysis, as well as designing and building innovative self-service solutions for insights generation from published resources and internal knowledge. This includes literature, patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. The Data Scientist should have sufficiently strong background in both science and technology to fulfil this role and demonstrate high motivation to expand their knowledge in a pharma context and as SME for key client groups. The role is expected to collaborate [. .. ] knowledge extraction from (full-text) publication resources Provide unique scientific insights and expertise by designing and developing solutions for finding, extracting, curating, and visualizing knowledge from published and internal data Monitor and be attuned to new technological trends relevant for knowledge analysis and insights discovery Achieve great results, while demonstrating key Abb Vie values and behaviors. Qualifications This is how you make a difference: Bachelors degree (7+ years of experience) , Masters degree (5+ years of experience) or Ph. D. degree [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate
• München
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 outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. Reconciles contents of the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor-CRA (m/w/d)
• München
CRA Germany-single client 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing [. .. ] defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct Bachelors degree in a related field or equivalent experience Minimum of 2-4 years of experience in clinical research monitoring Excellent communication and interpersonal skills Proficiency in using clinical trial management systems and other relevant [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• München
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 outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. Reconciles contents of the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate/ Klinischer Monitor (m/w/d)
• München
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 outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. Reconciles contents of the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor (m/w/d)
• München
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 outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. Reconciles contents of the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate (Klinischer Monitor)
• München
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 outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. Reconciles contents of the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, [. .. ]
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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 86 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Jobs?
Aktuell suchen 17 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:
- Thermo Fisher Scientific (9 Jobs)
- TFS Health Science (5 Jobs)
- Abb Vie (3 Jobs)
- PSI CRO (3 Jobs)
- Milestone One (2 Jobs)
- Fortrea (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 (19 Jobs), Rheinland-Pfalz (6 Jobs) und Hessen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
