42 Jobs für Clinical Trial Specialist
Stellenangebote Clinical Trial Specialist Jobs
Neu Job vor 4 Std. bei Neuvoo gefunden
Parexel
• Berlin
[. .. ] align, theres no limit to what we can achieve. Parexel is beginning to search for an experienced Senior Clinical Trial Administrator to join one of our key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sponsors in the Clinical Trial Specialist. In this role you will provide technical and administrative support to the clinical study teams responsible for clinical trial execution. Some specifics about this advertised role Support moderately complex clinical study activities in support of the Clinical Trial Manager. Work closely with the clinical trial team to ensure trial activities [. .. ]
Job vor 9 Tagen bei Mindmatch.ai gefunden
allaboutvienna
Healthcare Medical
• AT- 9 Wien
[. .. ] your skills and ambitions. Your next career move is just one upload away. Upload your CV and let our smart AI take care of the rest Corporate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Relations/ Key Account Specialist (m/f/d) The Cardiovascular and Interventional Radiological Society of Europe (CIRSE) is a non-profit making, educational and scientific association aiming to improve patient care through the support of. . . Permanent Austria-Wien 9 hours ago Patient Safety Lead (f/m/d) At Roche you can show up [. .. ] genuine connections, where you are valued, accepted. . . Permanent Iqvia Austria-Wien 9 hours ago Project Manager, Study Operations, Cronos Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an. . . Permanent Austria-Wien 9 hours ago Public Affairs Manager (f/m/d) Job Description Summary #LI-Hybrid Location: Vienna, Austria At Novartis, one of Austrias [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or related field [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 1-3 years clinical research experience German language proficiency is essential for direct communication with the Competent Authority and Ethics Committees. Good interpersonal communication and organizational skills. Good technology skills and knowledge of MS Office applications. Good attention to detail. General awareness clinical trial environment and drug development process. Ability to work on multiple projects. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. IQVIA is a leading global provider of clinical research services, [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
IQVIA
Regulatory Start Up Specialist I, IQVIA Med Tech, Austria
• AT- 9 Wien
[. .. ] Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or related field [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 1-3 years clinical research experience German language proficiency is essential for direct communication with the Competent Authority and Ethics Committees. Good interpersonal communication and organizational skills. Good technology skills and knowledge of MS Office applications. Good attention to detail. General awareness clinical trial environment and drug development process. Ability to work on multiple projects. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. IQVIA is a leading global provider of clinical research services, [. .. ]
Job am 14.11.2025 bei Mindmatch.ai gefunden
Medtronic plc
• AT- 9 Wien
[. .. ] include the following and other duties may be assigned: In this role you will carry out the responsibilities within the framework of contribution to multi-disciplinary teams including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support [. .. ] budget impact, and cost-of-illness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossier for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Freelance Senior/ Medical Director (Neurology-Bid Defense Support)
• Hamburg
Führungs-/ Leitungspositionen Freiberuflich
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 service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior/ Medical Director (Neurology-Bid Defense Support) . About this role TFS Health Science is seeking a highly flexible board-certified Neurology specialist to support upcoming Bid Defense Meetings. This freelance role involves contributing expert input during proposal preparation (e. g. protocol review) and participating in the Bid Defense Meeting itself. Ideally, the successful candidate would also be available for medical monitoring support if the project is awarded although this is not a [. .. ] a key scientific advisor in bid defense meetings (BDM) , RFP responses, and proposal development, ensuring compelling and medically sound strategies. Study Design Protocol Development : Provide expert input on trial design, patient recruitment, and regulatory strategy to optimize study success. Medical Oversight : Lead medical monitoring activities across assigned projects and step in as a handson medical monitor when needed. Scientific Advocacy : Represent TFS at client meetings, industry conferences, and scientific events, reinforcing our reputation as a trusted CRO [. .. ]
Job gestern bei Jobleads gefunden
• München, Bayern
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 service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management [. .. ] documentation. Team Client Engagement : Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications : Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise : Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge : Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation and internal SOPs. Adaptability : Comfortable working in fast-[. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. 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 clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] on medical issuesproviding clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical [. .. ] safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Homeoffice möglich
[. .. ] and the improvement of peoples quality of life. Your tasks Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of high-dimensional omics datasets (spatial, single-cell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible [. .. ] applying? If you have any questions, feel free to contact Anne Hoffmann, who will be happy to help. Our recruiting is decentralized-your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Cover letter Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Field Clinical Specialist-NRW
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
[. .. ] often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a patients unmet clinical needs. Its our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. Since 2017, Edwards TMTT launched more than 4 products transformational therapies in Europe led by its PASCAL and EVOQUE programs. Every patient is different-be an expert on our PASCAL device/ therapy and helppatients suffering from mitral and tricuspid diseases The Field Clinical Specialist is responsible for educating physicians on Pascal technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals/in assigned territories/ regions. Territory Germany (Düsseldorf, Köln, Bonn, Aachen) travelling required If you are considering relocating to the region, we are open to it and happy to support you [. .. ] on one technology. Responsible for upselling in key strategic accounts working in conjunction with Business Managers Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP. Responsible for certification of the centers, physicians and other related staff, as well as EW personnel and as outlined within EW SOP Validate software and hardware updates in the field as applicable Regularly reviews clinical support activities, changes in the market and assigned accounts, as [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Scientist for Bioinformatic Analysis (f/m/x)
• Leipzig, Sachsen
Homeoffice möglich
[. .. ] scientific knowledge and the improvement of peoples quality of life. Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of high-dimensional omics datasets (spatial, single-cell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible [. .. ] leave, flexi days, plus public holidays International Staff Service: Support with the relocation and integration process in Germany Our recruiting is decentralized-your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree abroad, we [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Scientist for Bioinformatic Analysis (f/m/x)
• Leipzig, Sachsen
Homeoffice möglich
[. .. ] and the improvement of peoples quality of life. Your tasks Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of highdimensional omics datasets (spatial, singlecell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible research Prepare [. .. ] applying? If you have any questions, feel free to contact Anne Hoffmann, who will be happy to help. Our recruiting is decentralized your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Cover letter Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Scientist for Bioinformatic Analysis (f/m/x)
• Leipzig, Sachsen
Homeoffice möglich
[. .. ] scientific knowledge and the improvement of peoples quality of life. Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of high-dimensional omics datasets (spatial, single-cell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible [. .. ] leave, flexi days, plus public holidays International Staff Service: Support with the relocation and integration process in Germany Our recruiting is decentralized-your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree abroad, we [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Global Trial Optimization Project Manager
A leading biopharmaceutical solutions organization in Switzerland seeks a Global
Trial Optimization
Specialist to support
clinical study planning and recruitment. Responsibilities include creating recruitment materials, managing recruitment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] vendors, and contributing to process improvements. The position offers comprehensive benefits including health insurance, a possible company car, and flexible paid time off. #J-18808-Ljbffr 70991054 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Wien
A global healthcare company in Austria is seeking a CTIS-team
Specialist to manage EU
Clinical Trial applications, overseeing user management and ensuring effective communication with regulatory authorities. Ideal [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] candidates will possess strong organizational and time-management skills, alongside a relevant degree in biology or related fields. The role offers competitive benefits and a flexible working environment. #J-18808-Ljbffr 70791311 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
CTIS (Clinical Trial Information System) - Team Specialist-Fixed-term (1 year)
• Wien
Homeoffice möglich
[. .. ] we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Position The Clinical Trial Information System Team (part of Product Development Regulatory Operations) enables the development of organizational and people capabilities of the future, we support and optimize the delivery of projects and initiatives to the organization both on the molecule and molecule-enabling portfolio. We are responsible for enabling the future of clinical [. .. ] boundaries to deliver medical solutions now in order to transform patients lives. Please note that this is a fixed term position for 1 year. The Opportunity: As a CTIS-team Specialist, you will manage the administration of the EU CTA CTIS User Management Create initial CTAs as well as any other post-approval activities during the whole CTA lifecycle (e. g. modifications, inclusion of additional countries) in CTIS: Support compilation submission activities as per defined process and instructions from relevant functions [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• München, Bayern
Clinical Operations
Specialist-Munich area Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we [. .. ] and Work Instructions. Assist Clinical Monitoring staff with site management activities, acting as a Sponsor representative for assigned studies and communicating with sites to ensure protocol compliance. Create and maintain Trial Master Files (TMF) and project files, including participation in file audits. Prepare and maintain site manuals, reference tools, and other documents. Maintain, update, and input clinical tracking information into databases. Track incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client. Manage shared [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Schweinheim, Nordrhein- Westfalen
[. .. ] include the following and other duties may be assigned : In this role you will carry out the responsibilities within the framework of contribution to multidisciplinary teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support [. .. ] including costeffectiveness, budget impact, and costofillness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossier for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• München, Bayern
Clinical Trial Associate/
Specialist (CTA/ CTA) Join to apply for the Clinical Trial Associate/ Specialist (CTA/ CTA) role at Progressive. Sie haben Erfahrung als Clinical Trial Associate/ Specialist [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (CTA/ CTA) und suchen den Sprung zu einem namhaften Pharmaunternehmen in München? Dann dürfte folgende Stelle sehr interessant für Sie sein. Responsibilities Enge Zusammenarbeit bzw. Unterstützung [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Meerbusch, Nordrhein- Westfalen
[. .. ] effectiveness, budget impact, and cost-of-illness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossiers for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Clinical Operations Specialist-Munich area
• München, Bayern
Clinical Operations
Specialist-Munich area Updated: Yesterday Location: DEU-Remote Job ID: 25103690 Clinical Operations Specialist-Munich area Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model [. .. ] Clinical Operations Policies, SOPs, and Work Instructions. Assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring protocol compliance. Create and maintain Trial Master File (TMF) and project files, including participation in file audits. Prepare and maintain site manuals, reference tools, and other documents. Maintain and input clinical tracking information into databases. Track clinical and regulatory documents and update for investigator sites, studies, and project team. Manage shared mailbox, process site requests and [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Executive Medical Director Clinical Development Endocrinology, Europe
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] for tardive dyskinesia, chorea associated with Huntingtons disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid-to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, [. .. ] Monitoring patient safety and the overall benefit-risk profile of investigational drugs throughout the clinical trials in collaboration with Drug Safety and Pharmacovigilance Leads analysis, interpretation, and presentation of clinical trial data to internal and external audiences e. g. decision making, regulatory submissions, and scientific disclosures including conference abstracts and publication of manuscripts Engage with and foster strong relationships with key opinion leaders and investigators to incorporate clinical insights into internal strategy and ensure optimal clinical trial execution Collaborate closely with [. .. ] of data and identification of evidence generation needs Adhere to Neurocrine Europe quality assurance system and compliance with the relevant SOPs Requirements: The appointed candidate will be a physician with specialist experience/ qualifications in endocrinology and/or a proven track record of clinical development in endocrinology products. MD qualified, ideally with specialist medical qualification in Endocrinology and previous experience in patient care At least 8 years experience in early or late stage clinical development in the pharmaceutical industry, ideally including experience [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Technical Solutions Innovation Lead (m/f/d)
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] Data Science Statistical Programming Lead role will make an impact: Technical Programming Expertise Develop or oversee the development of customized reports and applications in R for monitoring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and exploration of clinical trial data Identify, design, and implement technical solutions that improve efficiency and scalability, leading initiatives from proof of concept to business adoption to deliver measurable value Leadership People Development Lead, mentor and develop a team of technical programmers/ developers and data scientists Mentor and collaborate with colleagues across biometry functions on [. .. ] level: Mid Senior level Employment type: Fulltime Job function: Information Technology Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Viatris by 2x Get notified about new Technical Solutions Specialist jobs in Allschwil, Basel-Country, Switzerland. #J-18808-Ljbffr 69796570 [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Wien
[. .. ] may include the following and other duties may be assigned:In this role you will carry out the responsibilities within the framework of contribution to multi-disciplinary teams including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support [. .. ] budget impact, and cost-of-illness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossier for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
Contract Specialist-hybrid in Munich
• München, Bayern
Principal Sourcing
Specialist Syneos Health Contract Specialist hybrid in Munich Syneos Health is a leading fully integrated biopharmaceutical solutions organization that accelerates customer success. It translates unique
clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical affairs and commercial insights into outcomes to address modern market realities. The companys clinical development model places the customer and the patient at the centre of everything it does, continually simplifying work to make Syneos Health easier to work with and to work for. Whether you join us in [. .. ] of the clinical development process and legal and contracting parameters. Customerfocused and ability to manage challenging priorities and to remain flexible and adaptable in stressful situations. Excellent understanding of clinical trial process across phases IIIV and ICH GCP. Good understanding of clinical protocols and associated study specifications. Excellent understanding of clinical trial startup processes. Project management experience in a fastpaced environment. Good vendor management skills. Excellent written/ oral communication, presentation, documentation, interpersonal skills as well as strong teamorientation. Strong organizational skills [. .. ]
1 von 2Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Specialist pro Jahr?
Als Clinical Trial Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 42 offene Stellenanzeigen für Clinical Trial Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Clinical Trial Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Specialist Stellenangebote:
- Edwards Lifesciences (3 Jobs)
- allaboutvienna (1 Job)
- IQVIA Argentina (1 Job)
- IQVIA (1 Job)
- Medtronic plc (1 Job)
- Boston Scientific (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Specialist Jobs werden derzeit in Bayern (9 Jobs), Nordrhein-Westfalen (4 Jobs) und Niedersachsen (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Specialist Jobs?
Clinical Trial Specialist Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
