Clinical Trial Specialist Stellenangebote


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Stellenangebote Clinical Trial Specialist Jobs gefunden bei Jobbörse Stellen-Online

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Job vor 14 Tagen gefunden Miltenyi Biomedicine GmbH

IMP Manager- Clinical Trials (m f d) - Homeoffice, Vollzeit

• 51429, Bergisch Gladbach, 51429 Homeoffice möglich
MEHRCompany Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life- threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult- to- [...] T- cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. Job Description In the Clinical Trial Execution Service department you will support our study processes and activities in line with our go- to- market strategy for [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, and staff [...]
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Stellenangebote Clinical Trial Specialist Jobs gefunden bei Jobbörse JobMESH

Stellenangebote Clinical Trial Specialist Jobs bei JobMESH


Stellenangebot Clinical Trial Specialist Job bei Miltenyi Biomedicine GmbH Job vom 06.12.2024 Miltenyi Biomedicine GmbH IMP Manager- Clinical Trials (m f d) • North Rhine- Westphalia
MEHRCompany Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life- threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult- to- [...] T- cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. Job Description In the Clinical Trial Execution Service department you will support our study processes and activities in line with our go- to- market strategy for [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, and staff [...]
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Stellenangebote Clinical Trial Specialist Jobs gefunden bei Jobbörse Neuvoo

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Stellenangebot Clinical Trial Specialist Job bei Kinderspital Zürich Job vom 02.12.2024 Kinderspital Zürich

Clinical Research Coordinator 50- 80

• 8032 Zürich, CH
Vergütung / Gehalt: EUR 6666,-
MEHR[...] teams activities, including but not limited to Personnel administration and Accounting Support in the preparation of financial and annual reports for sponsors and regulatory authorities Organization of on- site, virtual and/ or hybrid meetings with sponsors, patient organizations and external clinical partners Assistance with documenting and sending out correspondences with Swiss Medic or material to external clinical partners and study participants Handling administrative matters related to study participants, including arranging transportation and reimbursement Ordering materials and reagents for researchers Your profile You have an understanding of the clinical trial process, clinical practice, and a familiarity with medical terminology You are enthusiastic about working in an interdisciplinary international team of [...] Assistance with documenting and sending out correspondences with Swiss Medic or material to external clinical partners and study participants Handling administrative matters related to study participants, including arranging transportation and reimbursement Ordering materials and reagents for researchers Albion Zairi HR Specialist+41 44 249 23 45 23833041 [...]
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Stellenangebote Clinical Trial Specialist Jobs gefunden bei Jobbörse Jobleads

Stellenangebote Clinical Trial Specialist Jobs bei Jobleads


Job vor 2 Tagen gefunden Executive Director Clinical Development • Dortmund, Nordrhein- Westfalen Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual [...] (s) , e. g. , Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]
Job vor 2 Tagen gefunden

VP Clinical Development

• Dortmund, Nordrhein- Westfalen
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual [...] designated asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]
Job vor 2 Tagen gefunden Executive Director Clinical Development • Leipzig, Sachsen Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual [...] asset (s) , e. g. , Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees, and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]
Job vor 2 Tagen gefunden VP Clinical Development • Leipzig, Sachsen
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual [...] asset (s) , e. g. , Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. Oversee and support all contacts to external experts, executive/ steering committees, adjudication committees, and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry. Successful [...]
Job vor 2 Tagen gefunden Clinical Research Associate (m/w/d) • Jena, Thüringen Work-Life-Balance
MEHRClinical Research Associate (m/w/d) Clinical Research We are offering a position in the medical device sector with ambitious and passionate people [...] cross- functional teams. As a fast- growing organization, we provide ample room for development and our remote work policy allows for more flexibility for our employees. About the position The Clinical Research Associate will assist in the conduct of clinical trial activities such as supporting the submission process, ensuring appropriate documentation, and preparing relevant trial- specific documents and communication with trial [...] and coffee as well as regular team sporting events Ready to apply? We look forward to receiving your application (cover letter and CV) at bewerbung occlutech. com. Only applications in English will be evaluated. About Occlutech Occlutech is a leading specialist provider of minimally invasive cardiac devices, with a mission to improve the quality of life for people with heart conditions. [...]
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Job vor 3 Tagen gefunden

Data Transparency Specialist Data Sharing, Anonymisation and Clinical Trial Disclosure (f/m/d. . .

• München, Bayern
MEHRYour responsibilities will include Redaction of clinical trial documents Anonymisation of individual patient data Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility Disclosure activities [...]
Job vor 3 Tagen gefunden Clinical Research Associates (all levels) - Germany • München, Bayern
MEHR[...] enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life- changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and [...] roles are permanent. The CRA: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on- site visits to assess protocol and regulatory compliance and manages required documentation. . Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH- GCP guidelines, applicable regulations and SOPs to [...]
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Job vor 10 Tagen gefunden

Principal Scientist Clinical Genomics (all genders)

• Darmstadt, Hessen
MEHR[...] team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Your Role: We have an exciting opportunity for a Scientific Associate Director to join our growing Clinical Genomics team In this role, you will collaborate with a global team of experts to advance implementation of clinical biomarkers [...] CDx experts across our clinical development portfolio. In your role you ll be the technical lead for clinical biomarker assay strategy definition, development, outsourcing and validation under CLIA/ CAP and GCLP. Furthermore, you ll contribute to set up of clinical trial related documents and you ll manage clinical biomarker projects within quality, timeline, and budget expectations. This permanent role is based in Darmstadt, Germany but can operate from other European locations. Who you are: PhD/ MD or equivalent degree Specialist in clinical genomics with excellent hands- on expertise in assay development, validation, implementation, and data QC/ interpretation 5- 10+ years [...]
Job vor 10 Tagen gefunden Entry Level Contract Specialist • München, Bayern
MEHRJob Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full- time, office- based and hybrid Contract Specialist to join our Clinical Operations team in Munich. This position plays a key role in the study start- up and clinical trial management processes at Medpace. The Site Contract Specialist will advance the start- up of our projects. If you want an [...]
Job vor 10 Tagen gefunden

Clinical Research Associates (experienced) - Germany

• München, Bayern
MEHR[...] enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life- changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and [...] roles are permanent. The CRA: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on- site visits to assess protocol and regulatory compliance and manages required documentation. . Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH- GCP guidelines, applicable regulations and SOPs to [...]
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