37 Jobs für Research Study Coordinator
Stellenangebote Research Study Coordinator Jobs
Job am 05.05.2026 bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical
study sites need and our overall mission is to support sites [...]
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[...] in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling and preparation for all types of monitoring visits at the medical institution/ research center. Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution. Track patient enrollment and actively support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Research Associate
Job Title: Field Clinical
Research Associate This role supports the Clinical Operations team by overseeing clinical studies, ensuring high-quality human
study data collection, and facilitating collaboration between internal study teams, [...]
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[...] contract research organizations, and clinical sites. You will take ownership of site monitoring and study oversight for multiple clinical studies, with a focus on software and medical device projects rather than pharmaceuticals. The position requires a flexible, detail-oriented professional who [. .. ] guidelines relevant to clinical research. Willingness and ability to travel when required for study needs, while supporting primarily virtual monitoring activities. Additional Skills Qualifications Experience similar to a clinical research coordinator, particularly in invoicing, data tracking, and trial closeout activities. Experience working with or for a contract research organization or in a sponsor role supporting clinical studies. Experience in clinical operations, clinical trial execution, or field clinical roles such as Field Clinical Research Manager or Field Clinical Specialist. Exposure to health [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
IRB Program Analyst (26001251) Temple Universitys
Research Administration Department is searching for an IRB Program Analyst Become a part of the Temple family and you will have access to the [...]
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[...] following: A hybrid work schedule Full medical, dental, vision coverage Paid time off 11 Paid Holidays Tuition remission eligible employees and their dependents can obtain a degree [. .. ] or regulatory compliance experience in a research or clinical setting. An equivalent combination of education and experience may be considered (e. g. , drafting and submitting IRB protocols as a study coordinator, grad student, etc. ) . Required Skills and Abilities Demonstrated knowledge and understanding of complex federal regulations, ethical issues, institutional policies, and other federal agency requirements governing human subjects research. Demonstrated computer skills, and proficiency with MS Word, MS Power Point, MS Excel or similar software programs. Demonstrated ability to [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Global Clinical Operations Lead (m/f/d)
• Luzern
Führungs-/ Leitungspositionen
[. .. ] m/d) to manage and oversee clinical trials/ clinical studies/ clinical investigations from initiation to close-out. This role will work closely with GC crossfunctional project teams, investigators, and [...]
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[...] Contract Research Organizations (CRO) to ensure that studies are conducted in compliance with applicable regulatory requirements, Good Clinical Practice (GCP) , and applicable institutional policies. Key responsibilities include ensuring the protocols are prepared and ensure that endpoints are aligned with the requirements for approval and for feasibility evaluations. Reporting to the Chief [. .. ] (R D) Officer, this role is critical in ensuring the timely execution of clinical trials/ clinical studies/ clinical investigations, the integrity of clinical data and the safety and wellbeing of study participants. This is a global senior individual contributor role with an initial primary focus on Europe, responsible for establishing and overseeing clinical operations processes in compliance with EU Medical Devices Regulation (MDR) 2017/ 745 and following the applicable ISO requirements. Key Responsibilities Study Coordination Prepare the study protocol; establishment of [. .. ] management systems. Excellent command of English is required; knowledge of additional languages will be considered an asset. Willingness to travel internationally as required. Preferred Qualifications Certification as a Clinical Research Coordinator recognized in the US or Europe. Proficiency in class III dental medical devices. Experience with clinical trials preparation, monitoring, tracking and reporting at CRO. Familiarity with electronic medical records (EMR) and patient data privacy regulations (e. g. , EU GDPR, U. S. HIPAA) . Success Metrics Ontime and compliant delivery [. .. ]
Job am 09.06.2026 bei Jobleads gefunden
• Hamburg
[. .. ] You will navigate the global landscape to find the best tech and product talent, ensuring our companies have the capabilities to remain market leaders. This isnt a [...]
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[...] seat for a coordinator; its a seat for a strategic talent partner who understands the nuances of modern tech stacks and the psychology of developers. The applike group is committed to creating engaging experiences for every app user around the world. We are passionate about creating market-changing products, technologies, and companies. We have [. .. ] roles. Tech: Ideally, you have a technical background (e. g. , a degree in Computer Science or former experience in a technical role) . Mindset: You treat sourcing like a research project. You are relentless in your pursuit of talent. Communication: Professional English skills with the ability to communicate complex ideas clearly to highlevel stakeholders. Adaptability: You thrive in an environment where performance is measured by impact, not activity. You value feedback and constant iteration. Fuel for the Journey: Benefits to [. .. ] team and company events, including hackathons and social gatherings. We work together, and we celebrate together, too. The Interview Process: 1st Interview with TA Manager 2nd Head of Talent Case Study 3rd Case Study Presentation 4th Get to know the Founder and VP of People We welcome applications from people who will contribute to the diversity of our company. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing [. .. ]
Job am 28.05.2026 bei Jobleads gefunden
CCCM Intern (Site Planning)
• Genf
[. .. ] IASC Humanitarian Reform. between CCCM, GBV and other specialized Protection actors; and improving womens participation in camp governance structures. Under the direct and overall supervision of the [...]
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[...] global CCCM Cluster Coordinator, the successful candidate will be responsible for supporting the CCCM team in the implementation of GFFO project activities and supporting in the development of various initiatives related to IOM CCCM globally, including tools, guidance and research. Responsibilities and Accountabilities: Support the capturing, writing up summaries and sharing of CCCM site improvement, development and site design case studies, lessons learned, and best practices, with focus on protection and GBV mainstreaming activities. Liaise with IOMs field colleagues on relevant CCCM and global project efforts, tools and initiatives; analyse [. .. ] cluster retreat, and simulation exercises. Perform such duties as may be assigned. Required Qualifications and Experience: Education Completed advanced university degree from an accredited academic institution in a field of study related to engineering, architecture, urban design, urban planning, or other relevant social sciences, Or the equivalent combination of a bachelor degree and previous humanitarian work experience in a related area. Prior experience in working on site planning, site improvements, forced displacement, disaster risk reduction, or protection issues is an asset. [. .. ]
Job am 28.05.2026 bei Jobleads gefunden
• Genf
[. .. ] IASC Humanitarian Reform. between CCCM, GBV and other specialized Protection actors; and improving womens participation in camp governance structures. Under the direct and overall supervision of the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global CCCM Cluster Coordinator, the successful candidate will be responsible for supporting the CCCM team in the implementation of GFFO project activities and supporting in the development of various initiatives related to IOM CCCM globally, including tools, guidance and research. Responsibilities and Accountabilities: Support the capturing, writing up summaries and sharing of CCCM site improvement, development and site design case studies, lessons learned, and best practices, with focus on protection and GBV mainstreaming activities. Liaise with IOMs field colleagues on relevant CCCM and global project efforts, tools and initiatives; analyse [. .. ] cluster retreat, and simulation exercises. Perform such duties as may be assigned. Required Qualifications and Experience: Education Completed advanced university degree from an accredited academic institution in a field of study related to engineering, architecture, urban design, urban planning, or other relevant social sciences, Or the equivalent combination of a bachelor degree and previous humanitarian work experience in a related area. Prior experience in working on site planning, site improvements, forced displacement, disaster risk reduction, or protection issues is an asset. [. .. ]
Job am 21.05.2026 bei Jobleads gefunden
Junior Clinical Research Associate
• Wien
Absolventen, Einsteiger, Trainees
Work-Life-Balance
Study start up CRA, Austria ICON plc is a world-leading healthcare intelligence and clinical
research organization. Were proud to foster an inclusive environment driving innovation and excellence, and [...]
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[...] we welcome you to join us on our mission to shape the future of clinical development. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the [. .. ] skills. Required Qualifications And Experience Bachelors degree in a scientific or healthcare-related field. Minimum of 1 year of experience in the clinical research field (e. g. , as Study Coordinator or similar) . In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60) . Fluency in German and English language. What [. .. ]
Job am 14.05.2026 bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
The Clinical
Research Nurse is responsible for providing clinical nursing care for all
study participants an accordance with departmental policies and procedures and established standards of nursing care [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and practice in Clinical Trial setting. Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Job am 05.05.2026 bei Jobleads gefunden
Clinical Research Associate
• Frankfurt, Hesse
Work-Life-Balance
The Clinical
Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of
study participants at [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have [. .. ] review process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential. Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trial-related [. .. ]
Job am 03.05.2026 bei Jobleads gefunden
• München, Bayern
The Clinical
Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of
study participants at [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have [. .. ] process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. , Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trialrelated systems [. .. ]
Job am 28.04.2026 bei Jobleads gefunden
Senior Tech TA Manager (f/m/d)
• Hamburg
[. .. ] You will navigate the global landscape to find the best tech and product talent, ensuring our companies have the capabilities to remain market leaders. This isnt a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] seat for a coordinator; its a seat for a strategic talent partner who understands the nuances of modern tech stacks and the psychology of developers. The applike group is committed to creating engaging experiences for every app user around the world. We are passionate about creating marketchanging products, technologies, and companies. We have already [. .. ] roles. Tech: Ideally, you have a technical background (e. g. , a degree in Computer Science or former experience in a technical role) . Mindset: You treat sourcing like a research project. You are relentless in your pursuit of talent. Communication: Professional English skills with the ability to communicate complex ideas clearly to highlevel stakeholders. Adaptability: You thrive in an environment where performance is measured by impact, not activity. You value feedback and constant iteration. Fuel for the Journey: Benefits to [. .. ] team and company events, including hackathons and social gatherings. We work together, and we celebrate together, too. The Interview Process 1st Interview with TA Manager 2nd Head of Talent Case Study 3rd Case Study Presentation 4th Get to know the Founder and VP of People Our mission is to create an inspiring work environment for amazing people to achieve extraordinary things. Be part of it Skip writing cover letters. Tell us about your most passionate personal project, your desired salary, and [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
Clinical Research Nurse
• Berlin
The Clinical
Research Nurse is responsible for providing clinical nursing care for all
study participants in accordance with departmental policies and procedures and established standards of nursing care [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and practice in Clinical Trial setting. Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
IQVIA
Clinical Trials Assistant 2 (m/w/d) , based in the Düsseldorf area
• Frankfurt, Hessen
Homeoffice möglich
[. .. ] Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] documentation of clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the team as Clinical Trials Assistant 2 (m/w/d) in full-time and work in a combination of office and home-office in the Düsseldorf area. Your responsibilities might include: Assist Clinical Research Associates (CRAs) and [. .. ] clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness. Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Assist with the tracking and management of Case Report Forms (CRFs) , queries and clinical data flow. Act as a central contact for the clinical team for designated project [. .. ] or pharmaceutical field or office management. At least 2 years of experience as Clinical Trials Assistant or in another administrative role in clinical research, e. g. as Project Assistant, Study Coordinator, Study Nurse. Excellent knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and Power [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
Senckenberg Gesellschaft für Naturforschung
• Frankfurt, Hessen
Senckenberg Leibniz Institution for Biodiversity and Earth System
Research (SGN) , headquartered in Frankfurt am Main, is seeking to fill the following position at the Senckenberg Biodiversity and Climate [...]
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[...] Research Centre (SBi K-F) , starting as soon as possible : Scientific Coordinator for IPCC TG-Data (f/m/d) (Full time/ part time) Location:Frankfurt am Main Employment scope: Full-time; part time Type of contract: Temporary, limited to 2 years Remuneration: Collective agreement of the state Hesse (TV-H) / E13 Senckenberg is one of the worlds leading research institutions in the [. .. ] the heart of Germany, which also hosts one of our most famous facilities, the Senckenberg Natural History Museum. The mission of the Senckenberg Biodiversity and Climate Research Centre is to study the complex interactions between biodiversity and climate change. Within Senckenberg, the International Science-Policy Unit serves as a bridge between scientific research and policy processes, with a particular focus on Multilateral Environmental Agreements (MEAs) and global environmental assessments. One of the o ffices major activities is supporting the work of [. .. ]
Job vor 10 Tagen bei Neuvoo gefunden
IQVIA
Experienced Clinical Trial Coordinator (m/w/d) , Home Office in Germany
• Frankfurt, Hessen
Homeoffice möglich
[. .. ] Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and [...]
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[...] documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer an exciting opportunity to join the team as Experienced Clinical Trial Coordinator (m/w/d) to work in home-office anywhere in Germany. Your responsibilities might include: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g. , Trial Master File (TMF) ) that track site compliance and performance [. .. ]
Job vor 10 Tagen bei Neuvoo gefunden
IQVIA
• Erfurt, Thuringia
[. .. ] Erfahrung in der klinischen Forschung gezielt in einer Teilzeitrolle einsetzen? Arbeiten Sie gerne patientennah und strukturiert? Zur Unterstützung einer laufenden klinischen Studie suchen wir ab sofort eine [...]
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[...] erfahrene:n Studienkoordinator:in/ Clinical Research Coordinator/ Study Nurse (m/w/d) für ein Studienzentrum in Erfurt. Rahmenbedingungen Arbeitszeit: 20 Stunden pro Woche Einsatztage: flexibel Vertragsdauer: ca. 6 Monate Start: kurzfristig möglich Ihre Aufgaben In dieser Rolle übernehmen Sie eine zentrale Funktion im Studienalltag und arbeiten eng mit dem Prüfarztteam zusammen: Koordination und Betreuung einer klinischen Studie unter [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
Iron Maxx Nutrition GmbH Co. KG
Office Operations Coordinator (m/f/d)
• Hürth, North Rhine- Westphalia
[. .. ] want to create an office environment that is professional, welcoming and well organized. To strengthen our internal operations, we are looking for a hands-on and service-oriented Office [...]
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[...] Operations Coordinator (m/f/d) who helps keep daily office operations running smoothly and supports our teams, guests and internal stakeholders. You will play an important role in creating a positive office experience, reliable support structures and smooth coordination across office, guest service, fleet, events and administration. Ready to perform? Your tasks [. .. ] for us to rest on our laurels-we are constantly working with the greatest passion to offer you supplements that inspire, work and taste great The integration of the latest study results and the evaluation of practical field research in cooperation with professional sports clubs and our customers have led to permanent innovation in the development of new sports and fitness nutrition at Iron Maxx Nutrition since the company was founded in 2004. In addition to the basics of sports nutrition in the areas of strength/ endurance, muscle building [. .. ]
Job am 07.06.2026 bei Neuvoo gefunden
Subject Well Inc.
• München- Flughafen, Bayern
Freiberuflich
[. .. ] completing clinical trials faster so innovative treatments can reach patients sooner. If you enjoy helping people and have strong communication skills, join our virtual team and contribute [...]
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[...] to meaningful medical research. We are currently seeking a Freelance Study Coordinator to support our team in handling unscripted patient calls related to oncology clinical trials. If you have a medical background, excellent communication skills, and experience in oncology or clinical research, this could be a great fit. Tasks About the role As an Onco-Companion Patient Recruitment, you will serve as [. .. ]
Job am 06.06.2026 bei Neuvoo gefunden
IQVIA
Studienassistenz/ Study Nurse (m/w/d) - Goslar
• Brunswick, Lower Saxony
Sie sind
Study Nurse, MFA mit Erfahrung in der klinischen Forschung oder Clinical
Research Coordinator (CRC) und suchen eine neue Herausforderung? Sie möchten Ihre Expertise in einem internationalen Umfeld [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] einbringen und aktiv zur Entwicklung innovativer Therapien beitragen? Dann sind Sie bei IQVIA genau richtig Als weltweit führendes Unternehmen in der klinischen Forschung bieten wir Ihnen die Möglichkeit, Teil eines engagierten Teams zu werden, das sich [. .. ]
Job am 06.06.2026 bei Neuvoo gefunden
IQVIA
Studienassistenz/ Study Nurse (m/w/d) - Goslar
• Goslar, Lower Saxony
Sie sind
Study Nurse, MFA mit Erfahrung in der klinischen Forschung oder Clinical
Research Coordinator (CRC) und suchen eine neue Herausforderung? Sie möchten Ihre Expertise in einem internationalen Umfeld [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] einbringen und aktiv zur Entwicklung innovativer Therapien beitragen? Dann sind Sie bei IQVIA genau richtig Als weltweit führendes Unternehmen in der klinischen Forschung bieten wir Ihnen die Möglichkeit, Teil eines engagierten Teams zu werden, das sich [. .. ]
Job am 06.06.2026 bei Neuvoo gefunden
IQVIA
Studienassistenz/ Study Nurse (m/w/d) - Goslar
• Mannheim, Baden- Württemberg
Sie sind
Study Nurse, MFA mit Erfahrung in der klinischen Forschung oder Clinical
Research Coordinator (CRC) und suchen eine neue Herausforderung? Sie möchten Ihre Expertise in einem internationalen Umfeld [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] einbringen und aktiv zur Entwicklung innovativer Therapien beitragen? Dann sind Sie bei IQVIA genau richtig Als weltweit führendes Unternehmen in der klinischen Forschung bieten wir Ihnen die Möglichkeit, Teil eines engagierten Teams zu werden, das sich [. .. ]
Job am 29.05.2026 bei Neuvoo gefunden
IQVIA
Clinical Research Coordinator/ Study Nurse (m/w/d) - Papenburg
• Papenburg, Lower Saxony
Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen Clinical
Research Coordinator/
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>Study Nurse (m/w/d) zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Papenburg. Diese Teilzeit-Position in 16 Stunden ist ab sofort zu besetzen, zunächst auf 6 Monate befristet. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien [. .. ]
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Job am 25.05.2026 bei Neuvoo gefunden
Sanofi
Junior Discovery Pharmacokinetics Outsourcing Partner VIE Contract
• Frankfurt, Hessen
Absolventen, Einsteiger, Trainees
Work-Life-Balance
[. .. ] 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 job About [...]
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[...] Sanofi Main responsibilities: Study Management: Serve as the study coordinator for the outsourcing and operationalization of preclinical PK and TK activities, ensuring scientific integrity, adherence to timelines, quality deliverables, and budget compliance. Central Point of Contact: Act as liaison for all discovery PK/ TK-related activities, both internal and external providing the team with high-quality data to support informed decision-making. Study Oversight: Supervise all phases of pharmacokinetic studies, including in-life operations, bioanalysis, and PK/ TK evaluation, conducted both in-house and at external Contract Research Organizations (CROs) . Provide scientific and technical guidance as needed. Cross-functional Collaboration: Work closely with internal drug formulation, in-life, and bioanalysis teams to ensure rigorous study planning and seamless execution. Digital Data Management: Configure study designs in the cloud-based platform Benchling and manage data imports into internal [. .. ]
Job am 20.05.2026 bei Job-Consult gefunden
Herman Medical Staffing GmbH
Clinical Nurse Coordinator-Wound Ostomy Care for Saudi Arabia
• Saudi Arabia/ sonstiges/ weltweit
clinical nurse
coordinator wound ostomy care for saudi arabia herman medical staffing gmbh saudi arabia standard of excellence state of the art prestigious leading hospital in the kingdom of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] saudi arabia is urgently looking for western educated trained and experienced clinical nurse coordinator wound ostomy care hospital the hospital is one of the best international healthcare standard hospitals in the kingdom of saudi arabia has a great reputation for delivering quality care excellence in healthcare and provides great teaching and research opportunities as well leading hospital through their commitment in providing excellent quality healthcare and exceptional patient care alike renowned through their dedicated team of internationally qualified experienced healthcare professionals and by their state of the art technology leading hospital in saudi arabia is urgently looking for passionate and dedicated wound [. .. ] wound and ostomy care wound ostomy care registered nurse with expertise and experience in wound ostomy care bachelor of science in nursing or equivalent nursing degree not less than years study duration from an accredited program specialist training along with post graduate specialist certification in wound ostomy care cwon wocncb wcn wound care nurse cwcn certified wound care nurse or similar equivalent specialist training certification post graduate diploma and or certification in stoma care wound management wcc wound care certification oms [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Research Study Coordinator pro Jahr?
Als Research Study Coordinator verdient man zwischen EUR 45.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Research Study Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 37 offene Stellenanzeigen für Research Study Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Research Study Coordinator Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Research Study Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Research Study Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Research Study Coordinator Stellenangebote:
- IQVIA (9 Jobs)
- Georgetown University in Qatar (2 Jobs)
- Parexel (2 Jobs)
- Iron Maxx Nutrition GmbH Co. KG (1 Job)
- Subject Well Inc. (1 Job)
In welchen Bundesländern werden die meisten Research Study Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Research Study Coordinator Jobs werden derzeit in Berlin (6 Jobs), Sachsen-Anhalt (5 Jobs) und Hessen (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Research Study Coordinator Jobs?
Research Study Coordinator Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
