108 Jobs für Clinical Trial Associate
Stellenangebote Clinical Trial Associate Jobs
Job vor 12 Tagen bei Neuvoo.com gefunden
Elixir Associates
• Berlin
[. .. ] currently partnering with a rapidly growing European biotech developing next-generation therapies in the critical-care/ cardiology space. The company is expanding its Clinical Operations team and seeking a [...]
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[...] talented Clinical Trial Associate to support their advancing clinical programs across multiple Phase 2 studies. About The Job: Reporting directly to the Head of Clinical Operations, the Clinical Trial Associate will play a key role in supporting the planning, execution, and oversight of global clinical trials. You will work cross-functionally with Clinical Operations, [. .. ]
Job vor 2 Tagen 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 member of the CTT. You will be part of a highly collaborative and cross-functional [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• 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/ medical programs. Lead national projects [. .. ] 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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
• 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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
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 member of the CTT. You will be part of a highly collaborative and crossfunctional team [. .. ]
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 lead within the clinical trial team (CTT) and support the other CTT functions such as biostats/ Dm/Pharmacology/ PV/ Clinical operations etc. Execute the clinical development [. .. ]
Job am 11.07.2025 bei Jobleads gefunden
Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, German. . .
• Baden- Württemberg
Führungs-/ Leitungspositionen
Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, Germany, or relocation to Germany (relocation assistance available) . #clientvacancy #director #pv oncology Together with a German member of INRALS [...]
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[...] (International Network of Recruitment Agencies in Life Sciences) , we are looking for an Associate Director Patient [. .. ] the global initiatives for Patient Safety and Pharmacovigilance (PSPV) and Risk Management (RM) pertaining to compounds at various stages of development. In this role, you will work closely with the clinical development department and will be involved in a very strategic and global function. TASKS RESPONSIBILITIES: Crafting proactive, patient-centric RM strategies tailored to designated compounds. Overseeing and executing all PV activities pertinent to assigned drugs, encompassing database setup, continual safety monitoring, and addressing safety concerns. Engaging in cross-functional collaboration [. .. ] and Global Patient Engagement to devise patient-centric benefit-risk evaluations for developmental compounds. Collaborating with Global Epidemiology and Medical Affairs to design safety-oriented post-authorization studies. Analyzing clinical trial safety data for incorporation into clinical trial reports and regulatory submissions. Providing medical-scientific insights into regulatory documents, including PSURs, DSURs, RMPs, and Clinical Overview Statements. Keeping senior management apprised of the safety profile of designated drugs and suggesting PV/ RM actions. REQUIREMENTS: Medical degree with clinical and/or clinical [. .. ]
Job gestern 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 [...]
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[...] 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 [. .. ] Right to work in the UK. Up to 2years of pharmaceutical industry experience or other relevant experience (NHS or Academic) . Good knowledge of the drug development process, specifically clinical trial/ research. Knowledge of international standards (GCP/ ICH, FDA, EMEA) . 12+ months monitoring experience required. Ability to travel domestically (and possibly internationally) as needed to study sites, training, and meetings. Minimum of 50 overnight travel may be required. What ICON can offer you: In addition to a competitive salary, ICON [. .. ]
Job gestern 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 [...]
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[...] you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II [. .. ] 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 smooth study conduct. Performing data review and resolution of queries to maintain highquality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelors degree in a scientific or healthcarerelated field. Minimum [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Neu- Isenburg, Hessen
Flexible Arbeitszeiten Betriebliche Altersvorsorge Work-Life-Balance
Die Rolle Als
Clinical Research
Associate (CRA) übernehmen Sie die Verantwortung für die Überwachung und Qualitätssicherung klinischer Studien. Dabei sind Sie die zentrale Schnittstelle zwischen Prüfzentren, Sponsor und [...]
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[...] internen Fachbereichen. Die Mission Die Sicherstellung von Qualität und Integrität bei der Durchführung klinischer Prüfungen, um die Sicherheit von Patientinnen und Patienten zu gewährleisten. Die Aufgaben Planen, durchführen und nachbereiten von Pre Study-, Initiierungs-, Monitoring- und Close-Out-Visiten gemäß Trial Monitoring Plan Überwachung der Site Performance und unterstützen der Prüfzentren bei Rekrutierung sowie studienspezifischen Rückfragen Kooperation mit den Bereichen: Medizin, Projektmanagement, Qualitätsmanagement und Datenmanagement für einen reibungslosen Studienablauf Begleiten von Audits und Inspektionen und unterstützen der Zentren bei deren Vorbereitung Was wir erwarten Abgeschlossenes naturwissenschaftliches oder medizinisches Studium oder Berufsausbildung [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Sponsor-Focused Clinical Research Associate-Remote/ Hybrid
• Wien
A
clinical research organization in Austria is seeking a Clinical Research
Associate to monitor clinical
trial sites and ensure compliance with protocols and safety regulations. The ideal [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] candidate will possess a university degree in a related field and be fluent in both German and English. This role offers a competitive salary, performance bonuses, and flexible work arrangements. If youre ready to advance your CRA career, apply [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• 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 with remote work opportunities. #J-18808-Ljbffr 73157191 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Site Relationship Manager
• Essen, Nordrhein- Westfalen
About this role 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
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 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Site Relationship Manager
• Hamburg
[. .. ] Relationship Manager role at TFS Health Science. 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 entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. About This Role The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by: understanding the local environment, creating and maintaining strong, longterm relationships with sites, supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated to [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Software Engineer KI (all genders)
• Bonn, Nordrhein- Westfalen
Homeoffice möglich
[. .. ] function Other Industries IT Services and IT Consulting Referrals increase your chances of interviewing at adesso SE by 2x Sign in to set job alerts for Summer [...]
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[...] Staff roles. Freelance Clinical Trial Site Coordinator Cologne, North Rhine-Westphalia, Germany 1 week ago Trainee-Programm Financial Consultant (BWL, Finanzen, VWL) (w/m/d) Cologne, North Rhine-Westphalia, Germany 5 days ago Pedagogical specialist-elementary school child care Cologne, North Rhine-Westphalia, Germany 1 day ago Working Student Finance Procurement (m/f/x) Cologne, [. .. ] Germany 1 week ago Cologne, North Rhine-Westphalia, Germany 2 days ago Social Pedagogical Assistant/ Child Care Worker Cologne, North Rhine-Westphalia, Germany 600.00-600.00 2 weeks ago Associate Account Development Specialist-Business Development Cologne, North Rhine-Westphalia, Germany 1 week ago Cologne, North Rhine-Westphalia, Germany 1 day ago Sankt Augustin, North Rhine-Westphalia, Germany 4 days ago Cologne, North Rhine-Westphalia, Germany 3 days ago Cologne, North Rhine-Westphalia, Germany 6 days ago UN Women: Coordination Analyst, [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
MSL Radioligand Therapy
• Rotkreuz, Zug
[. .. ] for the MSL Radioligand Therapy role at Novartis Get AI-powered advice on this job and more exclusive features. Summary Medical Scientific Liaison (MSL) is a field-based Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs Associate at Novartis, responsible for developing and leading scientific engagement and long-term relationships with Medical Experts and Key Stakeholders. The role strategically supports the development, launch, and commercialization of Novartis products through scientific exchange, soliciting external insights, responding to unsolicited requests, and implementing clinical and educational strategies. This position reports directly to the National MSL Lead. Major Accountabilities Engage with Medical Experts (MEs) to educate on medical/ scientific information Ensure appropriate identification/ mapping of MEs and Key Accounts and identify opportunities to involve MEs when specific medical needs arise Develop and execute ME engagement [. .. ] effective delivery of medical information and insights Develop, plan, implement, and timely execute field medical tactics and engagement plans, aligned with the brand strategy Support Novartis clinical research programs, optimize trial execution, and provide scientific educational support to potential and actual study sites in collaboration with clinical operations Facilitate Investigator Initiated Trial (IIT) process upon investigator request Serve as a medical resource to field matrix colleagues Qualifications MD, Pharm D or Ph D in health/ life sciences with a solid background in the [. .. ]
Job vor 6 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 focused [. .. ] 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 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Site Relationship Manager
• Kassel, Hessen
About this role 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Job vor 7 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 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Associate pro Jahr?
Als Clinical Trial Associate verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 108 offene Stellenanzeigen für Clinical Trial Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Associate Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Clinical Trial Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Associate Stellenangebote:
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (10 Jobs)
- ICON (5 Jobs)
- IQVIA (3 Jobs)
- Elixir Associates (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Associate Jobs werden derzeit in Nordrhein-Westfalen (16 Jobs), Bayern (12 Jobs) und Hessen (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Associate Jobs?
Clinical Trial Associate Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
