20 Jobs für Clinical Trial Analyst
Stellenangebote Clinical Trial Analyst Jobs
Job am 17.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
[. .. ] nurturing relationships with key medical experts in Southern Germany and Austria. Youll work closely with Key Opinion Leaders (KOLs) , physicians, and healthcare professionals (HCPs) to lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific discussions, support trial enrollment, and deliver educational programs and training. As the primary medical point of contact, you will leverage your scientific expertise to strengthen collaboration with the Key Account Management team and drive impactful customer engagement. Key Activities Building and maintaining strong peertopeer relationships with KOLs. Leading scientific discussions with KOLs and [. .. ] shape strategies with actionable tactics. Developing and delivering comprehensive product education and medicalscientific information. Supporting Key Account Managers (KAMs) in identifying and engaging influential experts in the field, and supporting clinical trials while ensuring compliance with local regulatory guidelines. Qualifications Proven experience in Medical Affairs or Medical Science in the aesthetics or dermatology field. Expertise in developing and delivering medical training programs. Demonstrated ability to operate compliantly in a fieldbased role, effectively collaborating within both the medical and commercial organizations. Strong [. .. ] We believe a flexible work environment is only attainable by building strong relationships based on trust with our employees. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Nordberg Medical by 2x. #J-18808-Ljbffr 69801330 [. .. ]
Job gestern bei Jobleads gefunden
Senior Analyst, Site Contracts and Budgets Germany, Poland, Portugal or UK FSP
• Berlin
When our values align theres no limit to what we can achieve. At Parexel we all share the same goal to improve the worlds health. From
clinical trials to regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] consulting and market access every clinical development solution we provide is underpinned by a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and are committed to making a difference. Parexel is currently seeking a Senior Analyst Site Contracts Budgets to join us in either Germany, Poland, Portugal or the UK dedicated to a single sponsor. This role will be part of the Site Contracts Budgets team working to execute the clinical site contracts and budgets process for sponsor clinical development programs from contract initiation to completion, [. .. ] arrange meetings, prepare agendas and meeting planning. Submit purchase requisitions where needed through SAP systems. Support the development and maintenance of guidelines, training programs, policies and procedures related to clinical trial contracts and budget. Support the Director and team in the management of other daytoday activities related to clinical contracts and budgets as requested. Requirements 35 years experience in the pharmaceutical or biotechnology industry in clinical site contracts and/or outsourcing management. Proficient with Excel and Power Point. Excellent verbal, written [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Biberach an der Riß, Baden- Württemberg
Führungs-/ Leitungspositionen
Principal Scientist as Biomarker Lead for Neuroscience and Mental Health Were looking for a motivated Principal Scientist to help shape the future of
clinical development in the field of neurodegeneration, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] psychiatry, and mental health. As a Principal Scientist, you will play a key role in driving innovative translational strategies across the entire clinical development pipeline, with the ultimate goal of being firsttopatients. In this strategic position, you will support the clinical drug research and [. .. ] Ensure timely delivery of stateoftheart scientific concepts, data measurements and analyses for decision making throughout clinical drug development and registration, including all necessary processes and documentation. Act as representative in trial and project teams and regulatory meetings. Lead clinical development trials and project overarching topics in Experimental Medicine, and represent the respective area of responsibility in internal and external initiatives/ working groups. Implement collaborations and strategic partnerships with external bodies, and organize and manage projects with external organizations such as CROs [. .. ] guaranteed to be considered. Step 2: Virtual meeting mid/end of January2026. Step 3: Onsite interviews beginning/ mid February2026. Seniority level Mid Senior level Employment type Parttime Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 73203770 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Scientific Informatics Business Analyst
• München, Bayern
Vacancy Scientific Informatics Business
Analyst Location Munich Hours Full-time The Consultant will support strategic projects primarily for pharmaceutical and Biotech clients. The Consultant will gather business requirements, analyse customer needs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and gaps to propose solutions for the desired state. He or she will interface with business users and client managers in conjunction with the [. .. ] have demonstrated the ability to gain the trust of customers. Thorough understanding in one or more of the following areas of the bio/ pharmaceutical industry Drug discovery and development processes Clinical trial design and data management Laboratory workflows Chemical biologics materials management Sample management Robotic systems integration and qualification Operations KPI and metrics tracking. Be knowledgeable about relevant Regulations and standards that govern the development of technical solutions such as GLP, GMP, 21 CFR Part11, Part210, Part820 regulations. Technical Skills Be familiar [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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, [. .. ] 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, UNTF to EVAW, Bonn, P-2 (Temporary Appointment) Bonn, North Rhine-Westphalia, Germany 5 days ago Cologne, North Rhine-Westphalia, Germany 3 days ago Bonn, North Rhine-Westphalia, Germany 3 days ago Overath, North Rhine-Westphalia, Germany 6 days ago Cologne, North Rhine-Westphalia, Germany 3 weeks ago Cologne, North [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
MSL Radioligand Therapy
• Rotkreuz, Zug
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] know the nature of your request and your contact information. Please include the job requisition number in your message. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology Industry Pharmaceutical Manufacturing #J-18808-Ljbffr 72920979 [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] job and more exclusive features. Description CRA Germany or Austria-single-client Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site [. .. ] or processes within area of responsibility. Requires practical knowledge of a professional area, typically obtained through education combined with experience. Seniority level Entry level Employment type Fulltime Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x #J-18808-Ljbffr 72511034 [. .. ]
Job am 09.12.2025 bei Jobleads gefunden
Senior Business Systems Analyst/ Product Owner
• Berlin
Work-Life-Balance
Senior Business Systems
Analyst/ Product Owner IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialise in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies. Join us on our exciting journey Job Overview Define the scope and objectives of business systems through research and collaboration with stakeholders. Analyse user needs and adjust [. .. ]
Job am 09.12.2025 bei Jobleads gefunden
[. .. ] and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The position as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Reimbursement Analyst (m/f/d) is an exciting opportunity to work with Medtronics Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our [. .. ] to marketbased overpayment depending on professional qualification and experience. Responsibilities In this role you will carry out the responsibilities within the framework of contribution to multidisciplinary teams 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 [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
Senior Statistical Programmer (Remote-Permanent Homebased)
• Frankfurt, Hesse
[. .. ] figures, listings, and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analyze and submit clinical data for all requested analyses. Main Responsibilities And Accountabilities Collaborate with study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADa M datasets, Tables, Figures, Listings and Analysis Submission content. Ensure the quality and accuracy thus submission readiness of clinical data [. .. ] output (tables, figures and listings) when not provided by CRO. Lead and oversee the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADa M format. Lead and oversee the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Work closely with clinical study teams to plan and execute activities to ensure project timelines are met with highquality deliverables. Additional Tasks Collaborate with CR [. .. ] medical treatments to help improve patient outcomes and population health worldwide. Learn more at https:/ / jobs. iqvia. com Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care #J-18808-Ljbffr 71992279 [. .. ]
Job am 24.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Schweinheim, Nordrhein- Westfalen
[. .. ] and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The position as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Reimbursement Analyst (m/f/d) is an exciting opportunity to work with Medtronics Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our [. .. ] 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 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 [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Medical Science Liaison-North Germany
• Bremen
[. .. ] will be pivotal in establishing and nurturing relationships with key medical experts in North Germany. Youll work closely with KOLs, physicians, and healthcare professionals (HCPs) to lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific discussions, support trial enrollment, and deliver educational programs and training. As the primary medical point of contact, you will leverage your scientific expertise to strengthen collaboration with the Key Account Management team and drive impactful customer engagement. You Will Mostly Work On Building and maintaining strong peer-to-peer relationships with KOLs Leading [. .. ] strategies with actionable tactics Developing and delivering comprehensive product education and medical-scientific information. Supporting Key Account Managers (KAMs) in identifying and engaging influential experts in the field, and supporting clinical trials while ensuring compliance with local regulatory guidelines. This is a highly collaborative role, where you will be a part of a cross-functional local team in the DACH region and Europe, as well as the global Medical Affairs team. As an early member of the Nordberg Medical team, youll [. .. ] believe a flexible work environment is only attainable by building strong relationships based on trust with our employees. Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 69958256 [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Meerbusch, Nordrhein- Westfalen
Senior Reimbursement
Analyst (m/f/d) - EMEA Medtronic Meerbusch, North Rhine-Westphalia, Germany At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day [. .. ] 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/ 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 [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Wien
Senior Reimbursement
Analyst (m/f/d) - EMEA page is loaded # # Senior Reimbursement Analyst (m/f/d) - EME Aremote type: Remotelocations: Mollsfeld, Meerbusch, Germany: Vienna, Vienna, Austriatime type: Full timeposted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on: Posted Todayjob requisition id: R51188At Medtronic you can begin a life-long career of exploration and innovation, while helping [. .. ] 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 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 [. .. ]
Job am 29.10.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] internal colleagues. He/ she will support the local Hospital Affairs Lead (HAL) and will be responsible for building peer to peer relationships with external experts and other [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stakeholders to provide clinical, scientific, and medical education in the territory. The SAM will support research initiatives, advisory boards, and other compliant scientific exchange activities to support Rhythms strategically aligned Medical Affairs Plan aimed at identifying and addressing the unmet needs of people living with rare genetic disorders of obesity. Responsibilities And Duties Responsible [. .. ] with rare genetic disease of obesity. Closely collaborate with Global Clinical Development and Operations on interactions with investigators participating in Rhythms clinical trials, investigator meetings and advisory boards. Support clinical trial execution attending to the needs of investigators. Triage pressure points that may impede progress of clinical studies to the cross functional team for timely resolution. Assist in identification and education of referral sites for clinical trials and investigators to drive trial enrolment. Develop and implement a novel scientific communication plan [. .. ] tackle tough challenges and have the courage to ask bold questions. We are eager to learn and adapt. Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 67447514 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Global Head of Clinical Development Patient Safety Solutions
• Holzkirchen, Bayern
Führungs-/ Leitungspositionen
Global Head of
Clinical Development Patient Safety Solutions Join to apply for the Global Head of Clinical Development Patient Safety Solutions role at Sandoz in Deutschland Global Head of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Development Patient Safety Solutions 1 day ago Be among the first 25 applicants Join to apply for the Global Head of Clinical Development Patient [. .. ] provide regular updates and feedback to stakeholders. Minimum Requirements What youll bring to the role: Experience 10-15 years experience in a Clinical Development Patient Safety stakeholder engagement or business analyst role. Proven track record in project management and stakeholder satisfaction related to Clinical Development Patient Safety. Tenure in a management role overseeing complex projects. Proven track record of developing and implementing Clinical Development Patient Safety technology strategies. Demonstrated ability to lead and mentor a dispersed technology team. Experience in regulatory [. .. ] stakeholder engagement and relationship management. Skills Expert knowledge of Clinical Development Patient Safety business processes and complexities Strong experience implementing and managing IT technologies supporting key business capabilities, incl. Clinical Trial Management Systems (CTMS) , Electronic Data Capture (EDC) , Safety Databases (e. g. , Argus, Aris Global) , and Signal Detection, etc. Deep understanding of clinical trial processes, regulatory requirements (e. g. , Gx P, ICH guidelines) , and safety data management. A proven track record of implementing digital solutions to [. .. ]
Job am 02.09.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
Global Head of
Clinical Development Patient Safety Solutions Global Head of Clinical Development Patient Safety Solutions Sandoz continues to go through an exciting and transformative period as a global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both [. .. ] channels to provide regular updates and feedback to stakeholders. What youll bring to the role: Experience: 10-15 years experience in a Clinical Development Patient Safety stakeholder engagement or business analyst role. Proven track record in project management and stakeholder satisfaction related to Clinical Development Patient Safety. Tenure in a management role overseeing complex projects. Proven track record of developing and implementing Clinical Development Patient Safety technology strategies. Demonstrated ability to lead and mentor a dispersed technology team. Experience in regulatory [. .. ] stakeholder engagement and relationship management. Skills: Expert knowledge of Clinical Development Patient Safety business processes and complexities Strong experience implementing and managing IT technologies supporting key business capabilities, incl. Clinical Trial Management Systems (CTMS) , Electronic Data Capture (EDC) , Safety Databases (e. g. , Argus, Aris Global) , and Signal Detection, etc. Deep understanding of clinical trial processes, regulatory requirements (e. g. , Gx P, ICH guidelines) , and safety data management. A proven track record of implementing digital solutions to [. .. ]
Job am 31.08.2025 bei Jobleads gefunden
Experienced Informatics Analyst
• München, Bayern
[. .. ] our Informatics team who will lead advanced analyses of methodological data to inform study design decisions. The Informatics team utilizes informatics principles and techniques to architect, mine, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analyze, and visualize clinical trial data to inform study design choices for pharmaceutical development. The informaticist will create predictive data models to identify and analyze patterns, then program compelling visualizations of the data to support feasibility strategies. The team is seeking an experienced candidate for a senior-level position to contribute new skills to our team, support team growth, and foster fellow analyst development. The Informatics Team is a highly collaborative team with members in both the Cincinnati and London offices. This team supports clinical operation, medical, and feasibility teams with advanced data query and analysis. The Informatics Team also works side-by-side business analytics and software engineering to architecture innovative data [. .. ]
Job am 29.08.2025 bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADa M datasets, Tables, Figures, Listings and Analysis Submission content. Collaborates with study teams to ensure the quality and accuracy [. .. ] output (tables, figures and listings) when not provided by CRO. Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADa M format. Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables. Additional tasks: Collaborates with [. .. ] outcomes and population health worldwide. Learn more at https:/ / jobs. iqvia. com Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Senior Statistical Programmer jobs in Frankfurt, Hesse, Germany. Associate Principal Statistical Programmer (m/w/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, [. .. ]
Job vor 10 Tagen bei Neuvoo gefunden
Zifo RnD Solutions
Scientific Informatics Business Analyst
• Munich, Bavaria
Vacancy Scientific Informatics Business
Analyst Location Munich Hours Full-time The Consultant will support strategic projects primarily for pharmaceutical and Biotech clients. The Consultant will gather business requirements, analyse customer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs and gaps to propose solutions for the desired state. He or she will interface with business users and client managers in conjunction with the [. .. ] have demonstrated the ability to gain the trust of customers. Thorough understanding in one or more of the following areas of the bio/ pharmaceutical industry: Drug discovery and development processes Clinical trial design and data management Laboratory workflows Chemical biologics materials management Sample management Robotic systems integration and qualification Operations KPI and metrics tracking. Be knowledgeable about relevant Regulations and standards that govern the development of technical solutions such as GLP, GMP, 21 CFR Part 11, Part 210, Part 820 regulations. Technical [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical trial analyst pro Jahr?
Als Clinical trial analyst verdient man zwischen EUR 40.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Analyst Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 20 offene Stellenanzeigen für Clinical Trial Analyst Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Analyst Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Analyst Jobs werden derzeit in Bayern (5 Jobs), Nordrhein-Westfalen (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Analyst Jobs?
Clinical Trial Analyst Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
