404 Jobs für Clinical Monitoring
Stellenangebote Clinical Monitoring Jobs
Job am 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] issues, and develop action plans. Verify informed consent procedures are performed and documented for each subject, protecting confidentiality and assessing safety and data integrity at investigator sites. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Based on the Clinical Monitoring/ Site Management Plan, assess site processes, conduct source document review, verify CRF data accuracy, resolve queries remotely or onsite, support data capture and electronic data capture compliance. Perform IP inventory, reconciliation, storage and security review, and confirm correct dispensing and administration of study product. Review Investigator Site File accuracy and [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
i- Pharm Consulting
Clinical Research Associate
• AT- 9 Wien
Work-Life-Balance
[. .. ] years of clinical research monitoring experience with demonstrated expertise in all aspects of CRA responsibilities. Fluency in English and German. Valid drivers license. Expert knowledge of GCP, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] FDA regulations, and clinical monitoring standards. Strong attention to detail, problem-solving abilities, and flexibility in a dynamic environment. Ability to work independently and collaboratively within a team. Proficiency in Microsoft Office; ability to learn study-specific software. Desirable Skills Experience mentoring or training junior CRAs. Strong customer focus and ability to build effective site [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] highly effective interpersonal and organizational skills. Demonstrate the following attributes: proactive, detail oriented, taskdriven and highly organized. Demonstrate the critical elements of GCPs and local regulations as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] they relate to clinical monitoring, IRB/ EC and Investigator responsibilities. Demonstrated ability in report writing and strong ability to critically understand clinical research documents. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Working Conditions Homebased 58, 000-96, 500 a year + Bonus Accommodations for persons with disabilities are available on [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] their goals. We are agile and driven to accelerate the delivery of therapies. Job Responsibilities Perform activities in compliance with Corporate and Clinical Operations Policies, SOPs, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Work Instructions. Assist Clinical Monitoring staff with site management activities, acting as a Sponsor representative for assigned studies and communicating with sites to ensure protocol compliance. Create and maintain Trial Master Files (TMF) and project files, including participation in file audits. Prepare and maintain site manuals, reference tools, and other documents. Maintain, update, and input [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Clinical Trial Lead (Project Manager) - Germany
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] add-on business for the future. May participate in bid defense meetings where presented as potential project manager. May be required to line manage other project management team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] members and clinical monitoring staff. Qualifications Bachelors Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ ICH guidelines and other applicable regulatory requirements. Strong organizational skills. Strong ability to [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] add-on business for the future. May participate in bid defense meetings where presented as potential project manager. May be required to line manage other project management team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] members and clinical monitoring staff. Qualifications Bachelors Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ ICH guidelines and other applicable regulatory requirements. Strong organizational skills. Strong ability to [. .. ]
Job am 19.11.2025 bei Jobleads gefunden
Clinical Trial Lead (Project Manager) - Germany
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] or addon business for the future. May participate in bid defense meetings where presented as potential project manager. May be required to line manage other project management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team members and clinical monitoring staff. Qualifications Bachelors Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ ICH guidelines and other applicable regulatory requirements. Strong organizational skills. Strong ability to [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Berlin
Führungs-/ Leitungspositionen
[. .. ] highly effective interpersonal and organizational skills. Demonstrate the following attributes: proactive, detail oriented, taskdriven and highly organized. Demonstrate the critical elements of GCPs and local regulations as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] they relate to clinical monitoring, IRB/ EC and Investigator responsibilities. Demonstrated ability in report writing and strong ability to critically understand clinical research documents. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Working Conditions Homebased. Accommodations Accommodations for persons with disabilities are available on request in respect of all aspects of [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Clinical Operations Specialist-Munich area
• München, Bayern
[. .. ] where everyone feels they belong through diversity of thoughts, backgrounds, cultures, and perspectives. Job Responsibilities Perform activities in compliance with Corporate and Clinical Operations Policies, SOPs, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Work Instructions. Assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring protocol compliance. Create and maintain Trial Master File (TMF) and project files, including participation in file audits. Prepare and maintain site manuals, reference tools, and other documents. Maintain and input clinical tracking information into databases. [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong. Job Responsibilities Responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
Clinical Operations Lead
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] effective interpersonal and organizational skills. Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized. Demonstrate the critical elements of GCPs and local regulations as they [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relate to clinical monitoring, IRB/ EC and Investigator responsibilities. Demonstrated ability in report writing and strong ability to critically understand clinical research documents. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Working Conditions Home-based 58, 000-96, 500 a year + Bonus Accommodations for persons with disabilities are available [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• Wien
[. .. ] years of clinical research monitoring experience with demonstrated expertise in all aspects of CRA responsibilities. Fluency in English and German. Valid drivers license. Expert knowledge of GCP, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] FDA regulations, and clinical monitoring standards. Strong attention to detail, problem-solving abilities, and flexibility in a dynamic environment. Ability to work independently and collaboratively within a team. Proficiency in Microsoft Office; ability to learn study-specific software. Desirable Skills Experience mentoring or training junior CRAs. Strong customer focus and ability to build effective site [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Clinical Operations Lead
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] highly effective interpersonal and organizational skills. Demonstrate the following attributes: proactive, detail oriented, taskdriven and highly organized. Demonstrate the critical elements of GCPs and local regulations as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] they relate to clinical monitoring, IRB/ EC and Investigator responsibilities. Demonstrated ability in report writing and strong ability to critically understand clinical research documents. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Working Conditions Home-based Accommodations for persons with disabilities are available on request in respect of all aspects of [. .. ]
Job am 27.09.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] and functions independently to conduct site monitoring responsibilities for clinical trials, providing oversight, leadership, and guidance to ensure compliance and quality. The Sr CRA works closely with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of Clinical Monitoring, CRAs, and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. Key Responsibilities Provide guidance, oversight, and feedback to the CRA team to ensure adherence to project [. .. ]
Job am 15.09.2025 bei Jobleads gefunden
CRA Germany-single client
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Summary Roles within Clinical Monitoring/ CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a [. .. ]
Job am 30.08.2025 bei Jobleads gefunden
Clinical Research Associate
• München, Bayern
[. .. ] selection, initiation, monitoring, site data review and closeout activities/ visits (remote and onsite) , as well as remote data checks, in accordance with the timelines specified in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the study specific Clinical Monitoring Plan (CMP) . Driving performance at the sites. Proactively identifying and ensuring timely resolution to study-related issues and escalates them as appropriate. Training, supporting, and advising Investigators and site staff in study-related matters, including Risk Based Quality Management (RBQM) principles. Development of recruitment plans with each site and [. .. ]
Job am 14.07.2025 bei Jobleads gefunden
Senior CRA
• München, Bayern
[. .. ] well as providing oversight, leadership, and guidance in the management and execution of clinical trial s to ensure compliance and quality. The Sr CRA works closely with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of Clinical Monitoring, CRAs, and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. KEY RESPONSABILITIES Provides guidance, oversight, and feedback to the CRA team to ensure adherence to project [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
Miltenyi Biomedicine
• Bergisch Gladbach, North Rhine- Westphalia
[. .. ] medicine or similar) ; a Ph D would be an advantage. You alreadyhaveseveralyearsof professional experience in clinical research and in the management of (international) clinical trials according [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to GCP. Experience in clinical monitoring is an advantage. Ideally, you have a solid background in immunology, hematology, oncology or autoimmune diseases and are strong interest in cell gene therapies. You are a self-starter, proactive, goal-oriented and are an experienced project team leader. You are naturally communicative and you communicate confidently and appropriately in [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
Thermo Fisher Scientific
CRA I/ CRA II-FSP Germany
[. .. ] communication and social skills and are looking to work in a collegiate environment where you want to take true ownership for your work. Perform and coordinate all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently. Benefit from award winning training programmes that will assist your technical and professional skills and knowledge Keys to Success: Education University degree in a life-sciences field Experience Minimum 6 months of independent, on-site monitoring experience in a [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Thermo Fisher Scientific
Senior CRA-FSP-Cell Gene Therapy
[. .. ] communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. Perform and coordinate all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently. Benefit from award winning training programmes that will assist your technical and professional skills and knowledge. Keys to Success: Education University degree in a life-sciences field Experience At least 4 years of independent, on-site monitoring experience in [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Excelya
Project Data Manager
[. .. ] guidelines and appropriate local and international legislation. Acts as Functional Lead for Data Management including primary DM contact for Sponsors and for internal liaison between Data Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Project Management, Clinical Monitoring, and other functional groups. Coordinate the work of the assigned Data Management team. Ensures launch, delivery and completion of all Data Management activities and milestones according to contractual agreement and relevant Standard Operating Procedures (SOPs) , guidelines, and regulations. Responsible for financial management of assigned projects, including revenue recognition, changes [. .. ]
Job vor 12 Tagen bei Neuvoo.com gefunden
Advanced Resource Managers
Clinical Research Associate
• Munich
[. .. ] If so, we are keen to hear from you Our leading CRO client is recruiting for a CRA to be based in Germany, performing and coordinating all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of the clinical monitoring and site management process. This position is offered on a 12 month contract basis initially, working 32 hours per week. Description: Work in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures Conducts site visits to assess protocol and regulatory compliance and manages required [. .. ]
Job vor 12 Tagen bei Neuvoo.com gefunden
Advanced Resource Managers
Senior Clinical Research Associate
• Munich
[. .. ] so, we are keen to hear from you Our leading CRO client is recruiting for a Senior CRA to be based in Germany, performing and coordinating all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of the clinical monitoring and site management process. This position is offered on a 12 month contract basis initially, working 32 hours per week. Description: Work in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures Conducts site visits to assess protocol and regulatory compliance and manages required [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Schwabe Group
Senior Regulatory Affairs Manager (m/w/d) Phytopharmaka
• Karlsruhe
Beratungs-/ Consultingtätigkeiten Teilzeit Homeoffice möglich
Sabbaticals 30+ Urlaubstage Work-Life-Balance
[. .. ] und Nachverfolgung von Zulassungs-/ Registrierungsunterlagen in enger Zusammenarbeit mit internen Fachabteilungen und externen Partnern Erstellung und Aktualisierung von Dossiers im e CTD-Format Betreuung europäischer Verfahren (MRP, DCP, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Worksharing, Super-grouping) Monitoring und Umsetzung aktueller regulatorisicher Anforderungen im Bereich pflanzlicher Arzneimittel Monitoring und Umsetzung von CCSI-Änderungen (Company Core Safety Information) Erstellung und Aktualisierung der Produktinformationen Fachliche Anforderungen: Sie verfügen über ein abgeschlossenes Pharmaziestudium oder vergleichbares naturwissenschaftliches Studium, gerne auch mit Promotion Erfahrung: Sie haben mehrjährige Berufserfahrung im Bereich Arzneimittelzulassung, idealerweise mit [. .. ] Manager (m/w/d) Phytopharmaka (ID-Nummer: 13389125) . Medizin Arzt Management Medical Pharmacology Doctor Ph D Pharma Industry medizinisch Pharmaindustrie Medikament Herstellung Produktion Homöopathie Studium ISO Zulassung Anwalt Communication Strategy Clinical Phyto Pharma Pharmaka Pharmazie QS 70858185 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Monitoring pro Jahr?
Als Clinical Monitoring verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Monitoring Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 404 offene Stellenanzeigen für Clinical Monitoring Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Monitoring Jobs?
Aktuell suchen 55 Unternehmen nach Bewerbern für Clinical Monitoring Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Monitoring Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Monitoring Stellenangebote:
- Tigermed (32 Jobs)
- Astra Zeneca (16 Jobs)
- Planet Pharma (11 Jobs)
- Bio Talent (11 Jobs)
- Tubulis GmbH (10 Jobs)
- Medpace (9 Jobs)
In welchen Bundesländern werden die meisten Clinical Monitoring Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Monitoring Jobs werden derzeit in Bayern (53 Jobs), Nordrhein-Westfalen (48 Jobs) und Baden-Württemberg (34 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Monitoring Jobs?
Clinical Monitoring Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
