42 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
[. .. ] the study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality and [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Clinical Research Associate
• Wien
[. .. ] the study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality and [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification contact sites to gauge interest, confirm contact details, and obtain relevant documents. Site qualification. Ensure selection of appropriate sites for assigned studies. Site startup with minimal [. .. ] regulatory teams. Conduct all remote and onsite monitoring activities through all study stages. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconcile its contents with the Trial Master File (TMF) ; and ensure sites archive essential documents per local guidelines. Document activities via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, retention, and awareness strategies; and enter data into tracking systems to monitor observations, status, and action items. Demonstrate diligence in protecting the confidentiality of each subject or patient. Review assigned site data, assist with data query resolution and missing data followup; analyze data using trend reports and site practices; ensure timely resolution of data queries; and use available hardware and software to [. .. ]
Job gestern bei Mindmatch.ai gefunden
VIROS
Back-Office Mitarbeiterin/ Trial Coordinator Clinical Research Associate (m/w/d)
• AT- 9 Wien
Das Vienna Institute for Research in Ocular Surgery (VIROS) sucht zur Komplettierung seines Teams einen Back-Office Mitarbeiter in/
Trial Coordinator
Clinical Research Associate (m/w/d) . Back-Office Mitarbeiter in/ Trial Coordinator [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Research Associate (m/w/d) 40 Wochenstunden/ 20 Wochenstunden Das erwartet Sie Koordination, Überwachung und Betreuung von klinischen Studien gemäß den gesetzlichen Vorgaben und unter Einhaltung von Studienprotokollen und ethischen Standards Durchführung von Monitoring Besuchen vor Ort [. .. ] in der klinischen Forschung oder in einer vergleichbaren Position ist von Vorteil Grundlegendes Verständnis von SOPs, ICH GCP, CTR (EU) No 536/ 2014, MDR (EU) 2017/ 745 Ausbildung als klinischer Monitor von Vorteil Sicherer Umgang mit MS-Office Teamorientierung und die Fähigkeit, in einem dynamischen Umfeld zu arbeiten Wir bieten Ihnen eine verantwortungsvolle, abwechslungsreiche Tätigkeit in einem jungen, motivierten Team Teilnahme an internationalen Kongressen, Möglichkeit an Weiterbildungen und Fortbildungen Beginn der Tätigkeit: ab sofort Gehalt Das tatsächliche Gehalt liegt bei 2. [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Fortrea
• AT- 9 Wien
Are you detail-oriented and passionate about supporting
clinical research operations? Join our team as an FSP Clinical Project Coordinator, where youll play a key role in enabling regulatory workflows across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical studies. This is a sponsor-dedicated, office-based position in Vienna offering meaningful exposure to global clinical development. Key Responsibilities Coordinate administrative tasks related to regulatory submissions. [. .. ] the preparation and review of study-related documentation. Liaise with internal teams to ensure timely updates and data accuracy. Assist in scheduling meetings, managing email communications, and organizing project files. Monitor timelines and elevate delays or issues to relevant stakeholders. Contribute to continuous improvement of administrative processes. Required Qualifications At least 1 year of work experience in a clinical trial environment. Some experience in clinical research preferred. Regulatory administrative background. Strong proficiency in Microsoft Office (Excel, Outlook, Word, Power Point) . High affinity for electronic systems and document management tools. Fluent in German and English (verbal and written) . Excellent organizational skills and attention to detail. What We Offer A [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Octapharma
Trainee Clinical Supply Chain (m/f/d) - Clinical R D-temporary
• AT- 9 Wien
Absolventen, Einsteiger, Trainees
Trainee
Clinical Supply Chain (m/f/d) - Clinical R D-temporary Job ID: 62828 Location: Wien, AT Job Level: Entry Level Job Category: Research and Development Employment Type: Temporary employment Become part [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of a vital chain and contribute to our common goal of making peoples lives better. Octapharma is one of [. .. ] Clinical R D Support the planning and coordination of Investigational Medicinal Product (IMP) distribution to clinical sites and depots in collaboration with Quality, Logistics, and study teams Enter, track, and monitor clinical orders and shipments in relevant systems to ensure timely supply Assist in managing clinical inventory, including stock levels, expiry dates, and reconciliation activities Contribute to the evaluation and documentation of deviations (e. g. temperature excursions) during storage and distribution Support forecasting activities by collecting and consolidating demand information and communicating updates to planning teams Collaborate with cross-functional teams to set up and maintain clinical supply plans aligned with study requirements Assist in preparing and maintaining clinical trial and supply-related documentation in compliance with regulatory requirements (e. g. e TMF, FDA, ICHGCP) Contribute to continuous improvement of supply chain processes and support ongoing clinical projects Interesting development opportunities after successful completion of the program Your expertise and ideal skill set Successfully completed studies in Supply Chain Management, Industrial [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Octapharma Austria
• AT- 9 Wien
Absolventen, Einsteiger, Trainees
[. .. ] shaping our vision to provide new health solutions advancing human life. Your main tasks and responsibilities You will rotate in different areas to build up experience and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] understanding of Octapharma Clinical R D Support the planning and coordination of Investigational Medicinal Product (IMP) distribution to clinical sites and depots in collaboration with Quality, Logistics, and study teams Enter, track, and monitor clinical orders and shipments in relevant systems to ensure timely supply Assist in managing clinical inventory, including stock levels, expiry dates, and reconciliation activities Contribute to the evaluation and documentation of deviations (e. g. temperature excursions) during storage and distribution Support forecasting activities by collecting and consolidating demand information and communicating updates to planning teams Collaborate with cross-functional teams to set up and maintain clinical supply plans aligned with study requirements Assist in preparing and maintaining clinical trial and supply-related documentation in compliance with regulatory requirements (e. g. e TMF, FDA, ICH-GCP) Contribute to continuous improvement of supply chain processes and support ongoing clinical projects Interesting development opportunities after successful completion of the program Your expertise and ideal skill set Successfully completed studies in Supply Chain Management, [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
Medical Director
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
The Medical Director will support
clinical trials across early to late development phases, contributing to clinical strategy, safety oversight, and data interpretation. This role involves collaboration across crossfunctional teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to deliver on clinical development goals and regulatory milestones. This is a Hybrid position. Key Responsibilities Draft and review clinical trial documents (protocols, IBs, ICFs, CSRs) . Serve as medical monitor for clinical trials, including oversight of external CROs. Oversee safety data reporting in coordination with safety and pharmacovigilance teams. Support study data interpretation, efficacy/ safety analyses, and DSMB activities. Contribute to clinical and regulatory strategies and interactions with health authorities. Engage with investigators, KOLs, and advisory boards. Represent medical input [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
A leading biopharmaceutical company is seeking a Medical Director in Basel, Switzerland to support
clinical trials across early to late development phases. This role involves drafting clinical
trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] documents, serving as a medical monitor, and overseeing safety data. Candidates should possess a medical degree and at least 5 years of experience in clinical research, including 3 years in oncology. The position is hybrid, enabling collaborative work across cross-functional teams to meet clinical development goals. #J-18808-Ljbffr 88847791 [. .. ]
Job am 04.04.2026 bei Jobleads gefunden
Medical Monitor (Gastroenterology)
• München, Bayern
[. .. ] 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 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] on medical issuesproviding clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Biontech
Associate Director Audit Management
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As Associate Director Audit Management, you will play a pivotal role in ensuring the quality and compliance of Bio NTechs
clinical trials and processes. As part of the Global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to [. .. ] reviews Execute audits as the lead auditor for non-contracted audits (remote or on-site) Develop robust Corrective and Preventative Action (CAPA) plans, track their completion, and assess effectiveness Additionally: Monitor trends in audit observations to identify areas for improvement Manage projects and relationships with audit vendors while supporting local health authority inspections Drive continuous improvement initiatives within audit management processes A Good Match: Academic degree in Life Sciences; advanced degree preferred (e. g. , Masters level) At least 10 years of clinical trial experience, including 6 years in clinical auditing within the region Proven leadership experience managing teams or projects for at least 3 years Deep knowledge of global GCP regulations and quality audit methodologies; oncology experience is an advantage Proficient in Microsoft Office software, Veeva, Share Point; excellent English communication skills (written [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Indero
• Unstrut- Hainich- Kreis; Thüringen Thueringen
Description The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned
clinical trials. The project manager II oversees and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs) , good clinical practices, regulatory and study-specific requirements. Project Manager II acts as the main line of communication to [. .. ] in an environment where you can grow your career alongside the company IMPACT AND RESPONSIBILITIES Client interactions Serve as primary contact for the Sponsor Provide efficient and timely updates on trial progress Lead client calls effectively Project planning Oversee and actively participates in the preparation of project deliverables such as; study plans, protocol, informed consent form, electronic case report form (e CRF) , tables/ listings/ figures (TLFs) , clinical study report. Participate in the planning and conduct of the Investigator s Meeting. [. .. ] with protocol and sponsor requirements, and that data review, query resolution, and database lock timelines are met. Quality and risk management Ensure assigned studies are audit ready at all times. Monitor the quality of study deliverables, (including vendor and Sub CRO deliverables) and address issues as they arise. Manage risk and control measures to assure project quality. Analyze discrepancies between planned and actual results. Review and approve responses to quality assurance audits. Project budget and timelines Control the project budget, with particular [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Allucent
Sr. Clinical Research Associate (Germany)
• Regierungsbezirk Köln; Westfalen Koeln
[. .. ] a last impact on patients worldwide. Together we. Find more information about our values. The role Bring your monitoring expertise to the forefront of innovation. We are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] looking for a Clinical Research Associate (CRA) to join our A-team. As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. As a CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. Youll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Neo Carbon
• Regierungsbezirk Kassel; Hessen Kassel, DE
Führungs-/ Leitungspositionen
[. .. ] teams, which includes IHC, Molecular Pathology, Genomics, Proteomics, and Flow Cytometry. As an individual contributor, the Director of Project Management for Specialty Lab Services plays a key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role in overseeing clinical and scientific project management teams within the business, creating and harmonizing project management processes across laboratories, overseeing multiple business segments and multi-site projects, collaborating with stakeholders, and driving streamlined and successful project management across SLS. This position requires a deep understanding of the scientific capabilities within SLS and strong [. .. ] biochemistry, medicine or similar field) preferred, OR MS in natural sciences with equivalent work experience. Project Management certification (PMI or similar) preferred. Minimum of 10 Years of experience in clinical trial services with pharma and biotech companies. This includes long-standing experience in prospective clinical trials and companion diagnostics performance studies using immunohistochemistry, genomics, proteomics, or flow cytometry methodologies Work experience in a regulated environment/ quality management system (e. g. GCLP) Excellent verbal and written communication and negotiation skills. Ability to [. .. ] team, contribute to the direction of the SLS business unit growth Acting as a project manager with responsibility for large scale projects including services from multiple business units with Discovery Monitor revenue of the SLS project management group Operational Excellence Harmonization: Facilitate transparent communication, foster collaboration, and ensure shared accountability across Operational Site Leaders, Project Managers, Laboratory Managers, Sample Management, Pathologists, QA and IT Design and implement a company-wide organizational project management structure in close collaboration with the operational site [. .. ]
Job am 15.04.2026 bei Jooble gefunden
Clinical Operations Specialist with focus on finance
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Operations Specialist with focus on finance Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center [. .. ] as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits Maintains, updates, and inputs clinical tracking information into databases Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client R esponsibility in financial tracking and administration Manages shared mailbox, processes site [. .. ] escalating study issues. Recruits and coordinates communication with clinical trial volunteers and patients, and follows applicable regulations globally and by region. Collaborates with cross-functional teams to develop study materials, monitor trial progress, and address any issues that arise during the study. Impact and Contribution Individual contributors who provide organizational related support or service (administrative or clerical) , as well as roles operating in support of daily business activities (e. g. , technical, production, or craft levels) . The majority of [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Clin Choice
• Deutschland Deutschland, DE
[. .. ] of both worlds and we think youll agree. Clin Choice is a rapidly growing global contract research organization. Were currently expanding our CRA network in Germany and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are seeking skilled Clinical Research Associates (CRA II and Senior CRA) interested in partnering with some of the worlds leading pharmaceutical companies in the field of biomedicine. If that sounds like you, we encourage you to submit your resume via our website wed love to hear from you Position Overview Clinical Research Associate As [. .. ] directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Up to 8 years of experience as a CRA. Strong knowledge of clinical trial operations, GCP/ ICH Guidelines, and other applicable regulatory requirements. Sound knowledge of medical terminology. Fluent in English and local language (s) . Proficiency in Microsoft Office (e. g. Word, Excel, Outlook) . Education and Experience: A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical [. .. ] clinical research areas and medical devices/ combination products. Relevant industry certifications preferred (i. e. , CCRA, RAC, CDE) . Clinical/ medical background a plus. Languages: Be able to converse and monitor in English and German. Must be able to converse and understand the documentation, monitoring, etc. in a reasonably confident manner to monitor in that. Ability to travel up to 80. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Avomind
Clinical Trial Operations Manager-Digital Cardiology and Heart Failure
• Berlin Berlin, DE
[. .. ] human voice to detect heart failure worsening earlier than ever before. Their vision? To extend the lives of people with cardiac conditions and improve their quality of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] life. Tasks As Clinical Trial Operations Manager, you will take operational leadership of our FDA clearance trial and oversee execution of multiple ongoing EU and US clinical studies. You will work closely with clinical investigators, CRO partners, medical team, product, and data science teams to ensure studies meet regulatory, scientific, and operational excellence standards. This [. .. ] development. Engage with principal investigators and KOLs, fostering long-term academic and clinical partnerships with leading institutions around the world. Ensure audit readiness and proactive risk management across all studies. Monitor study progress and budgets, prepare executive reports, and communicate risks and mitigation strategies to leadership. Contribute to scientific dissemination, including abstracts, publications, and conference presentations. Requirements Required Qualifications Bachelors degree or higher in Life Sciences, Medicine, Biomedical Engineering, or a related field 5+ years of experience in clinical research with [. .. ]
Job am 08.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Trial Manager/ Local Study Manager 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 [. .. ] and by example. Qualifications: Bachelors degree or higher degree in Health or Natural Sciences Three years of experience in clinical research. Experience in project management and certain time as field monitor or site coordinator. International experienced preferred. Fluency in German and English. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Excellent communication, presentation and interpersonal skills We are always excited to connect with great talent. This posting is intended for a possible upcoming opportunity rather than a [. .. ]
Job am 08.04.2026 bei Jooble gefunden
R D Where your curiosity drives the miracles of science
• Berlin Berlin, DE
Clinical Operations Study Country Lead-all genders Bring your passion for AI and data-driven thinking to clinical research that makes a real difference. If you re excited about using data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to drive smarter decisions and improve patient lives, we want to meet you About the job Were an R D-[. .. ] (QD) s and ICH/ GCP and regulatory guidelines directives. As Clinical Operations Study Country Lead, you are the strategic hub at country level connecting internal and external stakeholders to accelerate trial execution. You ll collaborate with: Globally: COSL, Data Management, Vendor Management, Study Medical Manager, Clinical Supply Chain Study Manager, Patient Recruitment Retention Lead, and other Core Study Team members Locally: Clinical Research Associates, Clinical Project Assistants, Medical Advisors, Site Engagement Leads, Start-Up Strategy Managers, Medical Science Liaisons, and more [. .. ] University degree in medicine, pharmacy, biology, biochemistry or related natural science Experience in clinical research is mandatory, preferably in combination with experience in project management and certain time as field monitor or site-coordinator. Solid knowledge of clinical development process and relevant therapeutic/ disease area (s) ; GCP certificate Soft skills: Strong skills in project management Data analytic skills and use of digital tools, platforms and systems Problem-solving and risk-management skills in a clinical study environment Change management skills [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Chapter 2
(Senior) Clinical Research Scientist-Digital Cardiology. . .
• Berlin Berlin, DE
[. .. ] 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 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d)
• Region Mittlerer Oberrhein, Württemberg; Regierungsbezirk Karlsruhe; Württemberg Karlsruhe, DE
[. .. ] 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 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
CRA II/ Sr CRA-FSP-Germany (m/f/d)
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
[. .. ] discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the world healthier, cleaner and safer. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Through our PPD clinical research services, we support clinical trials in more than 100 countries, delivering laboratory, digital and decentralized solutions that help bring life-changing therapies to patients faster. Our goal-driven teams combine and deliver startup activities for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our [. .. ] balance Permanent employment Full-time (40 hours/ week) About the Role This position is for experienced Clinical Research Associates with 2+ years of independent monitoring experience. You will manage clinical trial sites across Germany, ensuring studies are conducted in compliance with the protocol, ICH-GCP, applicable regulations, and company SOPs. Youll work autonomously, partner closely with investigative sites, and collaborate with project teams to deliver high-quality, inspection-ready clinical trials. What Youll Do Perform site monitoring activities (on-site and [. .. ] documentation, system updates, and administrative tasks Education Experience Bachelors degree in a life sciences related field or equivalent qualification Minimum 2 + years of experience as a Clinical Research Associate/ Monitor Valid drivers license Full right to work in Germany Fluency in German and English (C1 level) interviews will be conducted in German Knowledge, Skills Abilities Strong clinical monitoring skills with hands-on RBM experience Excellent understanding and application of ICH-GCP and applicable regulations Solid therapeutic area knowledge and medical [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Hays Professional Solutions GmbH
Clinical Trial Associate für den Bereich Quality Assurance (m/f/d)
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Angebote von Zeitarbeitsunternehmen
Ihre Aufgaben: Quality Oversight Systems Management:
Monitor compliance with quality guidelines in
clinical business areas and implement regional quality plans Identify potential gaps, recommend solutions, and escalate relevant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] issues Assist in maintaining and improving quality documents and processes Audit Inspection: Lead and support audit and inspection preparations, including document management and response coordination Ensure trial sites and teams are inspection-ready Consultation Collaboration:Serve as the primary quality consultant, providing guidance on regulatory requirements and risk management Support root cause analysis, CAPA processes, and audit planning Collaborate with quality teams to strengthen quality culture and resolve issues Process Improvement Metrics: Drive continuous improvement and process optimization [. .. ]
Job am 08.04.2026 bei Jooble gefunden
IQVIA
Senior Clinical Data Team Lead (Senior DTL) - FSP
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Führungs-/ Leitungspositionen
The Sr. CDM will lead and contribute to data management activities in support of Client s studies across all stages of
clinical drug development. Summary of Key Responsibilities Contribute [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to data management activities as a lead study data manager in support of Client s clinical studies Lead database build activities including leading cross-functional review of e CRF content, review of edit check specifications, and perform user acceptance testing Monitor data collection, coding, and cleaning by vendors through tracking of study metrics and targeted data reviews Oversight of database lock activities and ultimate archiving of study data Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory [. .. ] an outsourced CRO model; experience with drug development in rare genetic diseases preferred Expert knowledge of e Clinical processes, efficient design/ build of an EDC data management system and other Clinical Trial/ Data Management Systems Knowledge and understanding of regulations and industry/ adopted data standards such as CDISC, SDTM, and CDASH Experience working with Medidata Rave Experience using standardized medical terminology, including Med DRA and WHO Drug Experience working with MS Office Suite (Excel, Word, Power Point) and familiarity with MS Project Excellent [. .. ]
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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 42 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 (3 Jobs)
- Biontech (2 Jobs)
- Avomind (2 Jobs)
- VIROS (1 Job)
- Fortrea (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 (8 Jobs), Berlin (6 Jobs) und Hessen (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
