77 Jobs für Clinical Trials Associate
Stellenangebote Clinical Trials Associate Jobs
Job vor 2 Tagen bei StepStone gefunden
Otsuka Pharma GmbH
• Frankfurt am Main
Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten
[. .. ] to make a difference together For Otsuka Pharma Gmb H in the department Global Regulatory Affairs we are looking for a full-time employee to start as soon [...]
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[...] as possible as Associate Director Global Regulatory Affairs (m/f/d) The Associate Director Regulatory Affairs provides global regulatory expertise to pre-clinical, clinical, and commercial areas for investigational and marketed products and he ensures that regulatory/ competitive intelligence, or scientific/ regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. Furthermore the Associate Director Regulatory Affairs collaborates with Regulatory Management to establish clear regulatory pathways and creates accurate and [. .. ] they are aligned with the strategic approach developed by the cross functional team Designing programs for complete and accurate INd/CTA/ NDA/ MAA and other submissions and ensuring that clinical trials are designed to meet regulatory requirements Supporting development of strategies, drafts responses, and/or reviewing responses and documents intended for submission to health authorities to assure compliance with regulatory standards Reviewing submission documents for consistency and ensuring they are aligned with strategic approach developed by the team Interacting with regulatory [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
ICON
Senior CRA
• AT- 9 Wien
Work-Life-Balance
Senior CRA ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join [...]
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[...] us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Description 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 [...]
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[...] 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 [. .. ] oversight of the Lead CRA, to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA) . Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ] conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and riskbased monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA: Remote On-site Clinical Monitoring Pro
• AT- 9 Wien
A leading biopharmaceutical solutions organization in Vienna is seeking a
Clinical Research
Associate to oversee clinical
trials ensuring compliance and data integrity. Responsibilities include site qualification, monitoring, and documentation while [...]
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[...] providing superior patient support. Ideal candidates possess a degree in a related field, knowledge of clinical guidelines, and fluency in German. This role offers opportunities for personal and professional growth in a dynamic and inclusive work environment. [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] 9, 2025 Location: Vienna, 1, Austria Job ID: 25104265-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
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[...] clinical, medical affairs and commercial 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 [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project [. .. ] conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and riskbased monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Discover what our more than 29, 000 employees already know: work here matters everywhere. We work hard, and [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA single sponsor-Germany
• AT- 9 Wien
Updated: Yesterday Location: Vienna, 1, Austria Job ID: 25105750-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affairs and commercial 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 [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution: Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 10.03.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The Study Physician is a critical global role responsible for assuming medical oversight of
clinical trials within Clinical Development Operations. This position requires a qualified and clinically experienced physician who [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will provide comprehensive medical expertise throughout all phases of the trialfrom preparation and conduct to reporting. The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to the [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
Associate Medical Director-Oncology, Sponsor-Dedicated (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The Study Physician is a critical global role responsible for assuming medical oversight of
clinical trials within Clinical Development Operations. This position requires a qualified and clinically experienced physician who [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will provide comprehensive medical expertise throughout all phases of the trialfrom preparation and conduct to reporting. The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to the [. .. ]
Job gestern bei Jobleads gefunden
• Zürich Zuerich
Führungs-/ Leitungspositionen
The
Associate Director (AD) , Biostatistics, leads the full scope of statistical contribution to a
clinical development program. The AD provides statistical strategies for the clinical
trials [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and regulatory submissions, and is accountable for the statistical deliverables within the program. Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions Influence and [. .. ]
Job gestern bei Jobleads gefunden
Associate Director in Data Science, Digital Health Analytics and Innovation (all genders)
• Darmstadt, Hessen
Führungs-/ Leitungspositionen
[. .. ] biomarkers and endpoints within the Advanced Data Science team in the Data Sciences organization. You will lead the identification, development, and deployment of novel digital endpoints and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcome measures across clinical trials and life cycle management programs. Collaborating closely with the Global Digital Health organization, you will spearhead the design and validation of machine learningdriven algorithms and data processing pipelines that extract clinically relevant insights from highvolume digital health data sources, such as wearables, sensors and apps, mobile devices, and patientfacing applications. [. .. ]
Job gestern bei Jobleads gefunden
• Risch- Rotkreuz, Zug
[. .. ] partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address. About The [...]
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[...] Job As Marketing Associate-Respiratory VIE within our Marketing team, you will have the opportunity to learn about how marketing works in the pharmaceutical industry through involvement in the creation of materials and digital initiatives in agreement with the marketing strategy, our priorities, and needs. Join the team transforming care for people with immune [. .. ] Sanofis Work Abroad Program, i Move, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our i Move Work Abroad Program is a unique opportunity to make a difference through your work. #J-18808-Ljbffr 85535561 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Trial Associate-Drive Life-Saving Trials
• Lachen, Schwyz
A global healthcare company in Lachen, Switzerland is seeking a
Clinical Trial Assistant to support international clinical
trials. The role involves managing Trial Master Files, preparing documents, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assisting teams with regulatory submissions. The ideal candidate will have prior experience in clinical research or office management and be proficient in English. You will work with a dedicated team to produce life-saving medicines and contribute to impactful healthcare [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director Global Regulatory Affairs (m/f/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Jobbeschreibung The
Associate Director Regulatory Affairs provides global regulatory expertise to pre-
clinical, clinical, and commercial areas for investigational and marketed products and he ensures that regulatory/ competitive intelligence, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or scientific/ regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. Furthermore the Associate Director Regulatory Affairs collaborates with Regulatory Management to establish clear regulatory pathways and creates accurate and [. .. ] they are aligned with the strategic approach developed by the cross functional team Designing programs for complete and accurate INd/CTA/ NDA/ MAA and other submissions and ensuring that clinical trials are designed to meet regulatory requirements Supporting development of strategies, drafts responses, and/or reviewing responses and documents intended for submission to health authorities to assure compliance with regulatory standards Reviewing submission documents for consistency and ensuring they are aligned with strategic approach developed by the team Interacting with regulatory [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director Operational Excellence (m/f/d)
• Planegg, Bayern
Führungs-/ Leitungspositionen
Associate Director Operational Excellence (m/f/d) Permanent employee, Full-time Planegg (Germany) , Remote (Germany) Be part of our team We are seeking a highly experienced Associate Director of Operational Excellence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (GCP) to lead continuous improvement efforts across our clinical trial operations and ensure adherence to the highest standards of GCP compliance. The position will be within the Quality Assurance (QA) department. We are a dedicated QA team supporting our development of antibody-drug conjugates (ADCs) and clinical trials with a strong focus on reliable processes and patient safety. Working closely together, we ensure that quality and compliance are part of every step, from research to clinical application. Our team values open communication, practical problem-solving, and a shared responsibility for doing things right. If you enjoy working in [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Opfikon, Zürich Zuerich
Führungs-/ Leitungspositionen
A global biopharmaceutical company located in Zürich is seeking an
Associate Director of Biostatistics. This role involves leading biostatistical strategy for
clinical trials and regulatory submissions, requiring a Ph [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] D or MS with significant experience in drug development. The ideal candidate will demonstrate strong leadership in statistical methodologies and regulatory interactions. The successful applicant will also manage project-wide analyses and represent biostatistics in interactions with regulatory authorities. #J-18808-Ljbffr 85308948 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Marketing Associate-Respiratory-VIE Contract
• Rotkreuz, Zug
Marketing
Associate-Respiratory-VIE Contract Location: Switzerland, Rotkreuz Target start date: 01/ 07/ 2026 i Move, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates [. .. ] tomorrow. Sanofis Work Abroad Program, i Move, offers jobsassignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our i Move Work Abroad Program is a unique opportunity to make a difference through your work. #LI-EUR #J-18808-Ljbffr 85210279 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Associate Director, Biostatistics
• Glattbrugg, Zürich Zuerich
Führungs-/ Leitungspositionen
Associate Director (AD) , Biostatistics The Associate Director (AD) , Biostatistics, leads the full scope of statistical contribution to a
clinical development program. The AD provides statistical strategies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions Influence and [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Associate Director, FP A Lead, Germany (m/w/d)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-[. .. ] not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1600182 : Associate Director, FP A Lead, Germany (m/w/d) #J-18808-Ljbffr 85057859 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Marketing Associate-Respiratory-VIE Contract
• Rotkreuz, Zug
Marketing
Associate-Respiratory-VIE Contract page is loaded # # Marketing Associate-Respiratory-VIE Contractlocations: Rotkreuztime type: Full timeposted on: Posted Todaytime left to apply: End Date: July 17, 2026 (30+ days left [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to apply) job requisition id: R2847259Marketing Associate-Respiratory-VIE Contract Location: Switzerland, Rotkreuz Target start date: 01/ 07/ 2026i Move, [. .. ] Sanofis Work Abroad Program, i Move, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our i Move Work Abroad Program is a unique opportunity to make a difference through your work. #LI-EUR # Pursue progress, discover extraordinary Better is out there. [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Clinical Research Associate
• München, Bayern
This is what you will do: The
Clinical Research
Associate (CRA) has local responsibility for the delivery of the studies at their assigned sites and is an active [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] participant in the local study team (s) . The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO) , Study Start-Up (SSU) manager, Clinical Study Assistant [. .. ] Sees change as an opportunity to improve performance and add value to the business. Ability to look for and champion more efficient and effective methods/ processes of delivering quality clinical trials with reduced budget and in less time. Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. Proactivity and assertively when communicating with internal stakeholders and sites Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/ [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Sales Team Lead (Munich, Germany)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] Room A web-based cloud platform used by companies in a wide range of industries to ensure secure confidential document sharing for online due diligence, fundraising transactions, corporate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reporting, licensing, clinical trials, and other business goals. The role We are looking for an Associate Director, Corporate Sales, to accelerate our growth as the firstchoice VDR provider in Germany. Based in Munich and reporting to our Director of Business Development, Jens Hohnwald, youll lead a highperforming team to win new clients, expand into new verticals, and sustain our exceptional growth trajectory. We seek a proven [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Senior Statistical Programmer
• Frankfurt, Hesse
[. .. ] figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADa M datasets, Tables, Figures, Listings and Analysis Submission content. Collaborates with study teams to ensure the quality and accuracy [. .. ] additional statistical analyses including but not limited to: support responses to regulatory agencies, generate integrated summary of safety and efficacy, support publications and presentations, support planning and reporting of clinical trials via exploratory analyses of available data, Position Qualifications and Experience Requirements: Education BSc in Computer Science, Mathematics, Statistics or related area with relevant experience Experience At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/ pharmaceutical environment using SAS Software. Indepth understanding of [. .. ] Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Senior Statistical Programmer jobs in Frankfurt, Hesse, Germany. Associate Principal Statistical Programmer (m/w/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 84960764 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Trial Associate-Studentjob. ch
• Lachen, Schwyz
[. .. ] provide new health solutions advancing human life. Your Main Tasks and Responsibilities Set up and maintenance of Trial Master Files and Investigator Site Files according to Octapharma [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] SOPs Assist the Clinical Team in preparing clinical trial documents Prepare, distribute, file, and archive clinical documentation Review study files periodically for accuracy and completeness Assist in the organization of Investigator Meetings and participate Perform administrative tasks to support team members with clinical trial execution, as required Assists in development of SOPs Assist the [. .. ] and IRB/ LECs in accordance with ICHGCP, applicable regulations, company SOPs and check the documents for regulatory submissions Your expertise and ideal skill set Previous experience as CTA in international trials or similar experience in office management of international trials would be strongly preferred Fluent in both written and spoken English; preferably also in German Computer literacy Proficient in Word, Excel and Powerpoint Able to manage multiple and various tasks with positive attitude Able to prioritize workload with attention to details [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Associate Director, Biostatistics
• Opfikon, Zürich
Führungs-/ Leitungspositionen
Overview The
Associate Director (AD) , Biostatistics, leads the full scope of statistical contribution to a
clinical development program. The AD provides statistical strategies for the clinical
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>trials and regulatory submissions, and is accountable for the statistical deliverables within the program. Responsibilities Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence [. .. ]
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Job vor 11 Tagen bei Jobleads gefunden
Associate Director, Audit Strategy and Vendor Quality
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] aligned with ICH E6 (R3) , regulatory expectations, and company objectives. Lead the planning, conduct, and reporting of audits and assessments, ensuring consistency, quality, and timely delivery, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in partnership with Clinical Auditing team, Development Quality and business stakeholders. Identify, assess, and elevate quality risks, contributing to trend analysis, metrics, and evidencebased insights. Support continuous improvement initiatives by translating audit and inspection findings into actionable corrective and preventive actions, monitoring audit trends and identifying emerging risks. Support implementation of Quality by Design [. .. ] role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Onsite Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes siteessential, sitebydesign, fieldbased and remotebydesign jobs. The [. .. ] not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1600063 : Associate Director, Audit Strategy and Vendor Quality #J-18808-Ljbffr 84519130 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Associate pro Jahr?
Als Clinical Trials Associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 77 offene Stellenanzeigen für Clinical Trials Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Associate Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Clinical Trials Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Associate Stellenangebote:
- ICON (16 Jobs)
- IQVIA (4 Jobs)
- Otsuka Pharma GmbH (1 Job)
- Syneos Health (1 Job)
- TFS Health Science (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Associate Jobs werden derzeit in Hessen (14 Jobs), Sachsen-Anhalt (13 Jobs) und Bayern (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Associate Jobs?
Clinical Trials Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
