Clinical Support Associate Stellenangebote


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Stellenangebot Clinical Support Associate Job bei Oxford Global Resources Job vor 3 Tagen gefunden Oxford Global Resources

Freelance CRA- Medical Devices (German/ English)

• Frankfurt Freiberuflich
MEHR[...] we are looking for a Freelance CRA to come on board and join the team. This position is open for Freelance German speaking consultants with medical device experience who would have 0. 7 to 1 FTE availability to give them support in managing sites in Germany, Switzerland and Austria. Remote opportunity + Up to 80 travel is possible. Job Description As a CRA you will be responsible for managing clinical activities at study sites conducting studies for Medical Devices. You will perform site management and monitoring activities and act as [...] activities such as narrative writing, managing the CEC/ DSMB, etc. Prepares and coordinates submissions to regulatory authorities. May perform other activities as assigned. Requirements Higher education degree or equivalent education, training, and experience. +2 years experience as a Clinical Research Associate Experience in monitoring medical device studies. Fluency in English and German. Understanding of clinical research processes and regulations. Certifications such [...]
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Job vor 13 Tagen gefunden Associate Director Engineering- Device Technology (m/f/d) • Schaftenau, Tirol Führungs-/ Leitungspositionen
MEHRAssociate Director Engineering- Device Technology (m/f/d) Job ID: REQ- 10026381 Summary LOCATION: Schaftenau, TYPE: Hybrid Working, #LI Hybrid Are you [...] design input requirements, global component specifications, and design verification documents. Ensure device design development is delivered to a high quality following the design control process and applicable regulatory framework. Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support Regulatory Affairs to prepare medical device/ combination product pre- registration documents and provide input to answer health authority questions. Support [...]
Job vom 05.11.2024

Associate Director Engineering- Device Technology (m/f/d)

• Schaftenau, Tirol Führungs-/ Leitungspositionen
MEHR[...] and scientists who are responsible for the development of parenteral combination products to ensure that our delivery systems fulfill the highest customer expectations? If yes, then this is the opportunity for you The Device Technology Solution Center is seeking an Associate Director Engineering within the Global Device and Packaging Development (GDPD) department in Schaftenau, Austria. Job Description Key Responsibilities: Lead technical [...] design input requirements, global component specifications and design verification documents. Ensure device design development is delivered to a high quality following the design control process and applicable regulatory framework. Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support Regulatory Affairs to prepare medical device/ combination product pre- registration documents and provides input to answer health authority questions. Support [...]
Job vom 22.07.2024 Associate Medical Director ( Hematology ) - (, , Remote) Führungs-/ Leitungspositionen
MEHRAssociate Medical Director ( Hematology ) - (, , Remote) Sign up with scientific. today to see all content and to create a personalized stream of news, jobs and events, by defining keywords andfollowing your favorite content sources. Medical monitoring answering day to day medical and scientific questions, provide daily medical support to Parexel staff or site Safety monitoring Review and sign off adverse reports for accuracy and medical consistency, provide support [...] Update Reports, review and sign off data listings for safety data, review adverse events and concomitant medications coding for accuracy and consistency. Provide medical expertise and training to Parexel personnel, sponsor, or site Provide medical support for the preparation of clinical protocols, final study report, statistical summary reports Provide medical input into pharmacovigilance workflows and projects, feasibility studies, Data Monitoring, Committees [...]
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Job vom 19.06.2024

Neurology Medical Director (Associate/ Senior)

Führungs-/ Leitungspositionen
MEHRNeurology Medical Director (Associate/ Senior) Apply At Job Full Name First Name Last Name Email Whats App Number Upload CV Please upload CV in [...] and health. We push science forward by conducting groundbreaking research, developing ground- breaking treatments, and supplying our teams with the tools necessary to help each member of the team realize their professional ambitions. Our work encompasses laboratory, digital, and decentralized clinical trial services, with clinical trials carried out in more than 100 countries and the continuous development of innovative frameworks for [...] made throughout the application process. People who need assistance due to eyesight, hearing, mobility, or cognitive disabilities are a few examples of this. If you are a disabled job seeker or supporting a disabled person and need accommodations or accessibility support in order to apply for one of our openings, please give us a call at 1- 855- 471- 2255. In [...]
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Job vom 12.06.2024 Site Care Partner- FSP ( Germany) - (, , Remote)
MEHR[...] we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives. Job Purpose: The Site Care Partner II (SCP I) is the face of the client and therefore accountable for: Ensuring that sites receive necessary support and engagement issues are resolved. Being the main clients point of contact for investigative sites and accountable for site start- [...] to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies, and client pipeline opportunities under supervision. Experience required: Demonstrated experience in site management with prior experience as a Clinical Research Associate or Lead CRA. Demonstrated experience in startup activities through site activation. Demonstrated experience in conducting and close- out activities. Demonstrated [...]
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Job vor 5 Tagen gefunden QIAGEN GmbH

Senior Specialist (m/f/d) Clinical Quality Assurance

• Hilden bei Düsseldorf
MEHRQIAGEN GmbH sucht in Hilden bei Düsseldorf eine/n Senior Specialist (m/f/d) Clinical Quality Assurance (ID- Nummer: 11722002) . At the heart of QIAGENs business is a vision to make improvements in life [...] day. Position Description An exciting new role has arisen within the QIAGEN Manchester Quality Assurance team. The successful candidate will take on responsibility for quality and compliance oversight of the activities performed by the Clinical Affairs team at QIAGEN, in support of the testing and registration of diagnostic tests covering a diverse portfolio of indications. The scope of the trials is [...] QA audits of clinical study sites - Participate in the QIAGEN internal audit program - Review Clinical Affairs SOPs Position Requirements - Degree qualification in a relevant subject, or equivalent employment experience - Proven working experience as a Clinical Research Associate or similar with knowledge of relevant regulations, standards, guidelines and best practice - Desirable: working knowledge of In Vitro Diagnostic [...]
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Stellenangebot Clinical Support Associate Job bei Sanofi- Aventis Deutschland GmbH Job vom 29.10.2024 Sanofi- Aventis Deutschland GmbH Real World Evidence (RWE) Medical Lead General Medicines GSA- all genders • Berlin Führungs-/ Leitungspositionen Homeoffice möglich
MEHREvidence Based Medicine, Real World Evidence, Outcomes Research, Epidemiology, Public Health, Clinical Research Associate, pharmaceutical industry, biotechnological industry . Sanofi- Aventis Deutschland GmbH sucht in Berlin eine/n Real World Evidence (RWE) Medical Lead General [...] on millions of patients around the world. Join our General Medicines Medical Team in Germany, Switzerland, Austria (GSA) as the Real World Evidence (RWE) Medical Lead , where youll leverage your expertise in health sciences, epidemiology, and public health to support the development, launch, and commercialization of drugs. The Real- World Data Evidence Science (RWD ES) team, part of GBU Medical, [...]
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Jobbörse Stellenangebote Clinical Support Associate Jobs gefunden bei Jobbörse Neuvoo

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Job vor 5 Tagen gefunden Manpower CH

APM- Associate Project Manager

• Allschwil Angebote von Zeitarbeitsunternehmen
MEHR[...] brands- Manpower, Experis, and Talent Solutions- we assist companies from various industries in recruiting staff. We have been active in over 75 countries and territories for 75 years and are repeatedly recognized for our commitment. With locations throughout Switzerland, we support our clients in successfully implementing their orders and projects. (Associate) Project Manager (m/f/x) Basel Metropolitan Area Key responsibilities: Develops study specific plans for each assigned project. Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/ spreadsheets. Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements. Participates in ongoing training [...]
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Neu Job vor 7 Std. gefunden Associate Director, Oncology Therapeutic Group Führungs-/ Leitungspositionen
MEHR[...] patients, aiming to positively impact the health of 2. 5 billion people by the end of the decade. R D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. As an Associate Director of Global Regulatory Affairs, you will ensure the development and execution of global and/ or regional regulatory strategies for [...] Regulatory Therapeutic Area (TA) Head for the development of appropriate regional regulatory strategies and their delivery according to plans. Collaborate with the Early/ Medicine Development Team (EDT/ MDT) or GRL to ensure a robust regulatory strategy is in place to support the development program and meet the needs of key markets. Work closely with local/ regional commercial teams to secure the [...] have them, please still apply: Advanced Scientific Degree (PhD, MD, PharmD) . Knowledge of all phases of the drug development process in regulatory affairs. Capability to lead regional development, submission, and approval activities in local region (s) . Knowledge of clinical trial and licensing requirements in all major countries in the region and, ideally, knowledge of other key Agency processes globally. [...]
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Job gestern gefunden

Associate Director, Clinical Operations

Führungs-/ Leitungspositionen
MEHRJob Description- Associate Director, Clinical Operations (240041) Associate Director, Clinical Operations Job Number: 240041 Summary of Key Responsibilities Lead and manage integration of all project team activities, leveraging internal and development partner resources, expertise and knowledge, along with optimizing CRO resources, expertise and knowledge. Manage performance, development and growth of junior staff to support and guide them to improved efficiency and effectiveness at prioritization and problem solving; highly experienced as a line manager. Provide [...]
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Job gestern gefunden Sr. Clinical Research Associate (Germany) • München, Bayern
MEHRAt Allucent, we are dedicated to helping small- medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life- changing therapies to patients in need across the globe. We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A- team (hybrid / remote) . As a Sr. CRA at Allucent, you will independently [...] the project team and the site staff. Works in collaboration with Allucent Centralized Monitoring Team to evaluate risk- based monitoring activities to facilitate oversight of the study conduct at the sites and prevent issues. Identifies potential logistical/ practical problems and support Project team to create solutions/ contingency plans, with timeframes for resolution. Ensures the continuous maintenance of the Trial Master File [...]
Job gestern gefunden

Associate Director, Oncology Therapeutic Group

• Baar, Zug Führungs-/ Leitungspositionen
MEHR[...] patients, aiming to positively impact the health of 2. 5 billion people by the end of the decade. R D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. As an Associate Director of Global Regulatory Affairs, you will ensure the development and execution of global and/ or regional regulatory strategies for [...] Regulatory Therapeutic Area (TA) Head for the development of appropriate regional regulatory strategies and their delivery according to plans. Collaborate with the Early/ Medicine Development Team (EDT/ MDT) or GRL to ensure a robust regulatory strategy is in place to support the development program and meet the needs of key markets. Work closely with local/ regional commercial teams to secure the [...] disease area. Preferred Qualifications Skills: Advanced Scientific Degree (PhD, MD, PharmD) . Knowledge of all phases of the drug development process in regulatory affairs. Capability to lead regional development, submission, and approval activities in local region (s) . Knowledge of clinical trial and licensing requirements in all major countries in the region and, ideally, knowledge of other key Agency processes globally. [...]
Job gestern gefunden Associate Director, Quality Operations Global API • Boudry, Neuenburg Führungs-/ Leitungspositionen
MEHR[...] party manufacturers engaged by External Manufacturing within a cross functional team. To ensure that the Quality resources working on priority Virtual Plant Teams (VPTs) , or multiple VPTs are appropriate, effective and coordinated. For specified products, lead a team to support the release activities in accordance with the conditions of our manufacturing authorization and provide strategic oversight on the API release [...] as Transforming patients lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each [...]
Job gestern gefunden

Associate Director, Quality Operations Global API

• Boudry, Neuenburg Führungs-/ Leitungspositionen
MEHRAssociate Director, Quality Operations Global API Working with Us Challenging. Meaningful. Life- changing. Those aren t words that are usually associated [...] party manufacturers engaged by External Manufacturing within a cross functional team. To ensure that the Quality resources working on priority Virtual Plant Teams (VPTs) , or multiple VPTs are appropriate, effective and coordinated. For specified products, lead a team to support the release activities in accordance with the conditions of our manufacturing authorization and provide strategic oversight on the API release [...] as Transforming patients lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each [...]
Job vor 3 Tagen gefunden Scientific Associate Director Clinical Assay Strategy (all genders) - full/- part- time possible • Darmstadt, Hessen Führungs-/ Leitungspositionen
MEHR[...] order to help patients at every stage of life. Joining our Healthcare 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: In our Clinical Biomarkers Technology team we have an exciting opening for an Associate Director, Clinical Assay Strategy for biomarkers in circulation (and other body fluids) . You will work in highly inter- disciplinary development teams as well as with technology solution providers and academia to support phase I to post- launch biomarker needs. You will join a team of subject matter experts on protein and cellular [...]
Job vor 3 Tagen gefunden

Clinical Trial Associate

• Hamburg, Berlin
MEHRAt TFS Health Science, we are dedicated to advancing clinical research through innovative solutions and a commitment to quality. We provide tailored services across the clinical development lifecycle to deliver impactful results for our clients and the healthcare industry. Role Overview: We are looking for a Clinical Trial Associate to support TMF archiving and documentation activities on- site in Hamburg. This position involves organizing, reviewing, and maintaining physical TMF documents to [...]
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Job vor 4 Tagen gefunden Laboratory Associate Regulated Bioanalysis • Basel, Basel- Stadt
MEHR[...] assay readiness, data context enabling decision making and ultimately deliver robust and fit for purpose regulatory filings. The Opportunity This position is an excellent opportunity for a talented Laboratory Specialist to integrate into a dynamic lab team dedicated to the support of pre- clinical and clinical projects when complex bioanalytical assays or time- critical data are required. As part of the pRED organization you [...]
Job vor 4 Tagen gefunden

Laboratory Associate Regulated Bioanalysis

• Basel, Basel- Stadt
MEHRLaboratory Associate Regulated Bioanalysis Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global [...] assay readiness, data context enabling decision making and ultimately deliver robust and fit for purpose regulatory filings. The Opportunity This position is an excellent opportunity for a talented Laboratory Specialist to integrate into a dynamic lab team dedicated to the support of pre- clinical and clinical projects when complex bioanalytical assays or time- critical data are required. As part of the pRED organization you [...]
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