Clinical Trials Associate Stellenangebote


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112 Jobs für Clinical Trials Associate


Stellenangebote Clinical Trials Associate Jobs


Neu Job vor 4 Std. bei Jobleads gefunden

Associate Medical Director/ Medical Director

• 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 [. .. ]

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Job vor 5 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [. .. ]

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Job am 09.11.2025 bei Jobleads gefunden Associate Medical Director/ Medical Director • Hamburg 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 [. .. ]

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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 [. .. ]

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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 [. .. ]

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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 [. .. ]

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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 [. .. ]

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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 [. .. ]

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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 [. .. ]

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Neu Job vor 4 Std. 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 [. .. ]

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Job gestern 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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. [. .. ]

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Job gestern 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job gestern 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 [. .. ]

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Job gestern bei Jobleads gefunden Freelance Oncology CRA Flexible Austria Trials • 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 [. .. ]

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Job gestern 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 [. .. ]

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Job gestern 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 [. .. ]

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Job vor 4 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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Job vor 5 Tagen bei Jobleads gefunden Director Project Delivery Führungs-/ Leitungspositionen TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Director Project Delivery-home based in Poland, Portugal, Italy, Sweden or UK. About this role We are seeking an experienced and dedicated Line Manager to lead our Trial Master File (TMF) and Clinical Research Associate (CRA) functional teams within the dynamic Ophthalmology Business Unit. This critical role involves strategic oversight, team leadership and operational management to ensure the efficient execution of clinical trials and the maintenance of regulatory compliance. Key Responsibilities Team Leadership Line Management Provide strong leadership, mentorship, and line management to a team of TMF Specialists and Clinical Research Associates, fostering a culture of accountability, excellence, and continuous improvement. Manage day-to-day resourcing activities, including workload balancing, task delegation, and [. .. ]

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Job vor 5 Tagen bei Jobleads gefunden Clinical Trial Project Manager Our Mandant, an innovative biotech company in the clinical Phase 2 stage, is seeking a Clinical Trial Project Manager to oversee the execution of international clinical trials in [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the field of neurodegenerative and ophthalmologic diseases. Your Responsibilities Drafting and reviewing clinical trial documents, including study protocols, patient information, investigator brochures, study plans, manuals, and reports End-to-end execution of clinical trials, including comprehensive monitoring activities from study start-up through close-out Development of deviation plans; [. .. ] Fully remote work setup within Germany A role within a fast-moving and globally oriented biotech environment Direct communication structures and minimal bureaucracy Attractive performance-based bonus scheme Seniority level Associate Employment type Full-time Job function Science, Research, and Project Management Industries Biotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Constares Gmb H by 2x Get notified about new Clinical Trial Project Manager jobs in Germany. Cologne, North Rhine-Westphalia, Germany #J-18808-Ljbffr 72805908 [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden CRA Germany or Austria-single-client • München, Bayern Beratungs-/ Consultingtätigkeiten Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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. Impact and Contribution: Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden Medical Science Liaison Rare Tumors Switzerland (all genders) • Zug [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 72690196 [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden Customer Experience Manager, South Germany Munich, Germany; Nuremberg, Germany; Stuttgart, Germany • München, Bayern Customer Experience Manager, South Germany Level of position: Associate Director Position type: 60 field-based, 40 (home-) office based How will your role help us transform hope into reality? We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] are looking for a highly motivated and visionary personality who is interested in shaping the treatment of people suffering from a serious rare disease. As a Customer Experience [. .. ] leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit and follow us on X (formerly Twitter; Blueprint Meds) and Linked In. Blueflex is our operating model which optimizes culture, productivity, flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility. Blueflex allows [. .. ]

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Job vor 8 Tagen bei Jobleads gefunden Clinical Research Associate • Dortmund, Nordrhein- Westfalen 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 [. .. ]

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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 112 offene Stellenanzeigen für Clinical Trials Associate Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Associate Jobs?

Aktuell suchen 9 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)
  • ICON (6 Jobs)
  • TFS Health Science (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.


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Dauer: 0.0542 s., Vers. V.2025-d-2008-Ind-141