117 Jobs für Clinical Trials Associate
Stellenangebote Clinical Trials Associate Jobs
Job vor 3 Tagen bei Jobleads gefunden
• Frankfurt (Oder) , Brandenburg
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Medical Science Liaison Rare Tumour-Austria (all genders)
• Wien
[. .. ] regional, and national level. Serve as a scientific expert to the medical community and facilitate the appropriate exchange of scientific information. Communicate experts opinion and feedback on [...]
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[...] new data and clinical trends to Medical Affairs and translate this information into strategic recommendations to enhance science and advance patient care. Act as primary liaison to investigators interested in developing and performing investigatorinitiated research. Collaborate with the Clinical Operations organization to enhance patient enrollment in companysponsored clinical trials by identifying appropriate clinical trial sites, supporting clinical trial awareness, and interacting with investigators in ongoing studies. Serve as medical lead and provide scientific support at medical congresses, support national and European medical booths staffing, participate and lead clinical support, and facilitate medical discussions at advisory boards and local scientific/ [. .. ] empowers everyone to work their magic and champion human progress Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity Seniority level: Associate; Employment type: Fulltime; Job function: Research and Science; Industry: Pharmaceutical Manufacturing. #J-18808-Ljbffr 72699533 [. .. ]
Job am 02.12.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
Führungs-/ Leitungspositionen
Associate Medical Director/ Medical Director About Us The development of novel, effective and safe therapies for the treatment of cancer is one of the main challenges for modern medicine. We [...]
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[...] want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of [. .. ] that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full lifecycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Dortmund, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Essen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 04.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Leipzig, Sachsen
Führungs-/ Leitungspositionen
[. .. ] of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Your [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] mission Provide clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program. Lead development of clinical sections of trial and program level regulatory documents such as protocol amendments, imaging/ pathology/ DSMB charters, briefing books, BLA/ MAA, ODD, breakthrough applications etc. Act as clinical [. .. ] the Clinical Development leadership by providing medical input into the Clinical Development Plan. Contribute to development of disease clinical standards for new disease areas. Prepare and support reports on clinical trials such as abstracts/ manuscripts. Support preclinical functions and the Clinical Development leadership and the Chief Development Officer (CDO) to develop biomarker strategies. Identify and mitigate risks (technical, clinical, financial) to the program. Support pre-clinical development activities such as target Identification, asset selection; support in-licensing, out-licensing or partnering [. .. ]
Job am 13.09.2025 bei Jobleads gefunden
Medical Director Multiple Sclerosis
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] to advance our mission of transforming science into medicines for patients with disorders of the nervous system. The Opportunity In this role, you will lead and/or support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] early-stage clinical projects from entry into a human through proof of mechanism and proof of concept, to transform molecules into new medicines in an area with huge unmet medical needs. You will leverage your expertise to translate innovative molecules into potentially transformative therapies for patients with severe brain disorders. By marrying science [. .. ] external engagements with advisory boards, site investigators, health authorities, and other key stakeholders Provide clinical input to programs in discovery research Lead scientific communications and disseminate the results of clinical trials in the form of conference presentations and journal publications Who You Are You have an MD or Md/Ph D with a specialty in neuroimmunology, multiple sclerosis, or a similar field. Board certification and fellowship training or research experience in relevant areas is preferred You bring at least 5 years of [. .. ] has access to healthcare today and for generations to come. Our efforts result in millions treated with our medicines and billions of tests conducted with our Diagnostics products. Seniority level Associate Employment type Full-time Job function Research, Science, and Engineering Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing #J-18808-Ljbffr 61867989 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Research
Associate-FSP-Remote Join to apply for the Clinical Research Associate-FSP-Remote role at ICON Strategic Solutions. ICON plc is a worldleading healthcare intelligence and clinical research organization. Were [...]
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[...] proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to [. .. ] Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What You Will Be Doing Conducting site qualification, initiation, monitoring, and closeout visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Research Associate-Sponsor dedicated
• Frankfurt, Hesse
Work-Life-Balance
Overview CRA, Germany, sponsor dedicated 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Frankfurt, Hesse
We are looking for anexperienced freelance
Clinical Research
Associate (CRA) to strengthen our clients project Team near Frankfurt am Main. Your expertise inmonitoring clinical research projectsacross Phases I-IVis [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] crucial for overseeing and ensuring the quality of clinical trials. Your expertise is in demand Apply now. Ihre Aufgaben Ensuring compliance with trial protocol, GCP, and regulatory requirements Performing Source Data Verification (SDV) (CRF vs. source patient data) Generating precise site visit and communication reports Diligent documentation in the Trial Master File (TMF) Close collaboration, training, and clarification with Investigators/ [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director Regulatory Affairs EMEA-Fixed Term Contract
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Associate Director Regulatory Affairs EMEA-Fixed Term Contract Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to [...]
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[...] care for the needs of patients and our people is always the right thing to do. To achieve this goal, our [. .. ] Tackle rare and dynamic challenges As our Associate Director, Regulatory Affairs EMEA, you drive optimal EMEA regulatory strategies for assigned products during product development and manage EMEA regulatory objectives (nonclinical, clinical) in alignment with department and corporate goals. You work closely with crossfunctional project teams to support product development, global clinical trials and marketing approvals, while ensuring that EMEA regulatory strategies are implemented and EMEA requirements for the assigned projects are achieved. You will initially be focusing on some of Ultragenyx marketed/pipeline programs and the respective regulatory strategies including their execution. You possess appropriate knowledge of EMEA rules, regulations, and guidance [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Research Associate-FSP-Remote
• Frankfurt (Oder) , Brandenburg
Clinical Research
Associate-FSP-Remote ICON plc is a worldleading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and closeout visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Research Associate
• Stuttgart, Baden- Württemberg
Work-Life-Balance
CRA II Senior/ Lead
Clinical Research
Associate (CRA) Remote, Germany Are you an experienced CRA looking for your next significant career step within the German clinical landscape? Do [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you thrive in an environment that values a thoughtful approach to site management and prioritises employee well-being? If so, we have a great opportunity for you to join [. .. ] a range of compelling areas, including Oncology, Haemato-oncology, Rare Diseases, and other innovative fields. You will play a crucial role in ensuring the smooth and efficient conduct of clinical trials, working with a network of sites across Germany. What sets this team apart? Focus on Quality, Not Just Metrics : They champion a solid thought process in site management, understanding that effective collaboration and proactive problem-solving are paramount. The team empowers their CRAs to manage their sites effectively without [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt (Oder) , Brandenburg
Senior CRA ICON plc is a worldleading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] join us on our mission to shape the future of clinical development. Role: Clinical Research Associate (12+ months monitoring experience required) Location: Must be based in the UK, ideally in the Midlands or South West of the UK (nationwide travel) Fully sponsor dedicated. As a Clinical Research Associate you will be dedicated to one of our global pharmaceutical clients, a sciencebased company with one of the [. .. ] have the opportunity to build your career in a customerfocused environment that supports creativity, collaboration and performance. Your responsibilities include, but are not limited to: Allocation, initiation and conduct of trials: conduct site selection, recommend sites, and act as the frontline liaison between ICON and sites to ensure successful collaboration and meet milestone and delivery expectations. Manage assigned study sites and networks, conduct phase IIV protocols according to the monitoring plan and client procedures, perform Site Initiation Visits, and ensure personnel is [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Research Associate
• Köln, Nordrhein- Westfalen Koeln
Work-Life-Balance
CRA II Senior/ Lead
Clinical Research
Associate (CRA) Remote, Germany Are you an experienced CRA looking for your next significant career step within the German clinical landscape? Do [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you thrive in an environment that values a thoughtful approach to site management and prioritises employee well-being? If so, we have a great opportunity for you to join [. .. ] a range of compelling areas, including Oncology, Haemato-oncology, Rare Diseases, and other innovative fields. You will play a crucial role in ensuring the smooth and efficient conduct of clinical trials, working with a network of sites across Germany. What sets this team apart? Focus on Quality, Not Just Metrics : They champion a solid thought process in site management, understanding that effective collaboration and proactive problem-solving are paramount. The team empowers their CRAs to manage their sites effectively without [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Wien
Freiberuflich
A leading healthcare staffing company is seeking a
Clinical Research
Associate (CRA) with oncology experience for freelance opportunities in Vienna, Austria. The role involves participating in innovative oncology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical trials and offers flexibility and competitive compensation. Ideal candidates should have proven experience in oncology clinical trials and strong knowledge of GCP and regulatory requirements. This role supports advancements in cancer research while providing professional growth opportunities. #J-18808-Ljbffr 73143020 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Associate in Analytical Research and Development for Oligonucleotides
• Penzberg, Bayern
[. .. ] and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Behind every Roche [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] product, whether in clinical trials or on the market, stands Pharma Global Technical Operations, a global organization with over 10, 000 employees committed to delivering safe and high-quality medicines. Pharma Technical Development, a key part of this effort, is dedicated to developing innovative solutions for new therapies to meet patient needs. Within Pharma Technical [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Remote Freelance Clinical Research Associate Dermatology Pediatric Trials
• Wien
Freiberuflich
A leading health care consultancy in Austria is seeking a Freelance
Clinical Research
Associate (CRA) to join their expanding clinical operations team. The ideal candidate will manage clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trial monitoring activities, ensuring compliance with guidelines and site management, while maintaining relationships with investigators. Proficiency in both German and English is preferred, alongside prior experience in Dermatology or Rare Paediatric Diseases. This role offers flexibility [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Freelance Clinical Research Associate
• Wien
Freiberuflich
Get AI-powered advice on this job and more exclusive features. Direct message the job poster from EPM Scientific Vice President-Recruiting in the
Clinical Operations, Clinical Development and Medical Affairs [...]
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[...] space across Europe EPM Scientific is currently partnered with a CRO client running a project in Austria. They are urgently seeking an experienced Freelance CRA to support their expanding clinical operations team. Contract Conditions Start date: ASAP/ January Location: Remote, Austria Contract Type: Freelance/ Consultant-0.2 FTE Duration: 12 Months Language: German English preferred Project: Dermatology/ Paediatric Rare Disease Key Responsibilities Perform monitoring activities for clinical trials in compliance with ICH-GCP and local regulations. Ensure proper site management and maintain strong relationships with investigators and site staff. Review source documents and verify CRF data accuracy. Track study progress and ensure timely resolution of queries. Collaborate with project managers and clinical teams to ensure high-quality deliverables. [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Research Associate
Clinical Research
Associate page is loaded # # Clinical Research Associatelocations: Germany Remotetime type: Full timeposted on: Posted 14 Days Agojob requisition id: R31245Be One continues to grow [...]
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[...] at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/ hematology clinical trials within the assigned region. The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Associate Director Regulatory Affairs
Führungs-/ Leitungspositionen
This position is posted by Jobgether on behalf of a partner company. We are currently looking for an
Associate Director Regulatory Affairs in Switzerland. In this role, you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] play a key part in shaping and executing regulatory strategies across the EMEA region for innovative therapies addressing rare diseases. You will operate in a dynamic, science-driven environment, working closely with cross-functional teams to support late-stage development, global clinical trials, and post-marketing activities. Your expertise will directly influence regulatory success, patient access, and long-term product sustainability. This position offers a balance of strategic leadership and handson execution within a collaborative and missiondriven setting. You will engage with global and regional stakeholders while navigating complex regulatory frameworks. The role [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Director, Regulatory Affairs CMC Europe
• Zug
Führungs-/ Leitungspositionen
[. .. ] submissions and manage the delivery of approved technical documents in accordance with project timelines. Manage the preparation, authoring, and maintenance of regulatory submission documents pertaining to CMC [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data for global clinical trial and marketing applications as well as postmarketing variations. May require technical regulatory authoring of submission package components. Support the evaluation of manufacturing changes for potential impact on products. Provide expert review of CMC documentation supporting regulatory submissions and communications. Coordinate preparation of responses to queries from regulatory authorities, particularly [. .. ] and/or interns. Develop and implement regulatory operating guidelines and common work practices/ strategies within the team. Qualifications 1012 years of related work experience (Director candidates typically bring 12 years; Associate level candidates may be considered with 10 years and strong potential) , including 8 years in Regulatory Affairs CMC in the biotech/ pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus. Proven experience serving as a primary RACMC contact to health [. .. ] outside partners. Excellent oral and written communication skills. Excellent organizational skills and attention to detail. Hybrid Work #LIHYBRID Key Skills Proofreading Adobe Acrobat FDA Regulations Manufacturing Controls Biotechnology Clinical Trials Research Development GLP c GMP Product Development Chemistry Writing Skills Employment Type Full Time Experience Years: 1012 Vacancy 1 Equal Opportunity Employer Cytokinetics is an Equal Opportunity Employer. Fraud Warning Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate [. .. ]
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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 117 offene Stellenanzeigen für Clinical Trials Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Associate Jobs?
Aktuell suchen 8 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:
- CCS- Global (11 Jobs)
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (9 Jobs)
- ICON (5 Jobs)
- Elixir Associates (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Associate Jobs werden derzeit in Nordrhein-Westfalen (18 Jobs), Bayern (12 Jobs) und Niedersachsen (10 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Associate Jobs?
Clinical Trials Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
