119 Jobs für Regulatory Affairs Associate
Stellenangebote Regulatory Affairs Associate Jobs
Job vor 13 Tagen bei Jobware gefunden
TRB Chemedica AG
• Feldkirchen bei München
Homeoffice möglich
30+ Urlaubstage
[. .. ] (m/w/d) Marketing Communications Manager Healthcare (m/w/d) Content Manager Healthcare/ Pharma (m/w/d) Commercial Product Specialist (m/w/d) Clinical Product Manager (m/w/d) Medical
Affairs Manager (m/w/d) Scientific Product Specialist (m/w/d) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Science Liaison (m/w/d) (mit leichter Marketingnähe) Medical Content Specialist (m/w/d) Event Congress Manager Healthcare (m/w/d) Healthcare Communications Manager (m/w/d) Education Training Manager Medical Devices (m/w/d) Digital Product Manager Healthcare [. .. ] Content Strategist Content Creation Manager Pharma SEO/ SEA Manager Healthcare UX Content Manager Med Tech Healthcare E-Commerce Manager Digital Communications Manager Pharma Marketing Automation Specialist Healthcare Scientific Affairs Specialist Clinical Research Associate (mit Produktfokus) Medical Information Specialist Evidence Data Manager Healthcare Clinical Evidence Manager Med Tech Regulatory Product Communication Specialist Medical Event Manager Healthcare Training Coordinator Medical Congress Coordinator Education Specialist Medical Devices Health Communications Specialist Corporate Communications Manager Healthcare 71621652 [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Syneos Health
Clinical Research Associate II
• blumenholz, MV
Clinical Research
Associate II/ Sr CRA-Full Service-ONC + Gen Med (Home-Based in Central US) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] translate 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 that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, [. .. ] Qualifications: Bachelors degree in a related field or equivalent experience Minimum of 2-4 years of experience in clinical research monitoring Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements Excellent communication and interpersonal skills Ability to work independently and manage multiple priorities Proficiency in using clinical trial management systems and other relevant software Certifications: Certified Clinical Research Associate (CCRA) or equivalent certification preferred Necessary Skills: Attention to detail and strong analytical skills Problem-solving abilities and critical thinking [. .. ]
Job vor 12 Tagen bei Neuvoo.com gefunden
Jazz Pharmaceuticals
• Munich
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
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[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree of cross-functional collaboration, and the ability to influence stakeholders across all levels [. .. ] between strategic vision and hands-on execution within a dynamic, fast-paced environment. The incumbent is also responsible for ensuring that all activities are conducted in full compliance with national regulatory and legal requirements, as well as Jazz Pharmaceuticals internal policies and healthcare compliance standards. Essential Functions Leadership and Development of the German Oncology MSL Team Build and lead a high-performing MSL team by consistently applying and exemplifying Jazzs high-performance practices. Establish and maintain effective performance management practices, ensuring [. .. ]
Job am 03.12.2025 bei Neuvoo.com gefunden
Jazz Pharmaceuticals
Associate Director, Head of MSL Oncology, Germany
• Munich
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree of cross-functional collaboration, and the ability to influence stakeholders across all levels [. .. ] between strategic vision and hands-on execution within a dynamic, fast-paced environment. The incumbent is also responsible for ensuring that all activities are conducted in full compliance with national regulatory and legal requirements, as well as Jazz Pharmaceuticals internal policies and healthcare compliance standards. Essential Functions Leadership and Development of the German Oncology MSL Team Build and lead a high-performing MSL team by consistently applying and exemplifying Jazzs high-performance practices. Establish and maintain effective performance management practices, ensuring [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Associate Director, Head of MSL Oncology, Germany
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree of crossfunctional collaboration, and the ability to influence stakeholders across all levels of [. .. ] a balance between strategic vision and handson execution within a dynamic, fastpaced environment. The incumbent is also responsible for ensuring that all activities are conducted in full compliance with national regulatory and legal requirements, as well as Jazz Pharmaceuticals internal policies and healthcare compliance standards. Essential Functions Leadership and Development of the German Oncology MSL Team Build and lead a highperforming MSL team by consistently applying and exemplifying Jazzs highperformance practices. Establish and maintain effective performance management practices, ensuring clear expectations [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
MSL Radioligand Therapy
• Rotkreuz, Zug
[. .. ] apply for the MSL Radioligand Therapy role at Novartis Get AI-powered advice on this job and more exclusive features. Summary Medical Scientific Liaison (MSL) is a field-based [...]
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[...] Medical Affairs Associate at Novartis, responsible for developing and leading scientific engagement and long-term relationships 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 requests, and implementing clinical and educational strategies. This position reports [. .. ] aligned with country strategy Respond to unsolicited requests for information from MEs Inform and shape medical strategy by collecting impactful insights from MEs Collaborate cross-functionally with clinical, commercial, and regulatory teams to ensure alignment and 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 [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
• München, Bayern
[. .. ] lists, Insight Assurance is one of the fastestgrowing global audit firms, with 170+ professionals supporting nearly 2, 000 clients across the Americas, EMEA, and APAC. Position Summary [...]
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[...] The ISO Manager Associate Manager are responsible for operating, supporting, and developing the ISO Practice with a high level of quality, productivity, and satisfaction for both clients and employees. This role oversees the delivery of ISO certification services, ensures compliance with accreditation requirements, and leads the development of the audit team to drive efficiency, [. .. ] within the practice. The role also serves as a Subject Matter Expert (SME) for senior leadership and crossfunctional teams, ensuring that audit operations align with strategic goals, client expectations, and regulatory standards. Key Responsibilities Leadership Operational Management Lead the ISO audit practice, ensuring highquality delivery, compliance, and efficiency. Manage ISO auditors, trainees, and interns, providing coaching, performance feedback, and career development support. Conduct planning calls with clients, verify application accuracy, and ensure effective engagement execution. Perform technical reviews of audit reports [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Director, Regulatory Affairs CMC Europe
• Zug
Führungs-/ Leitungspositionen
[. .. ] advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting to [...]
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[...] the Executive Director Regulatory Affairs CMC, the Director of Regulatory Affairs CMC is responsible for leading regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of U. S. and international regulatory submission strategies. Responsibilities Formulate CMC regulatory strategies without supervisor oversight based on current regulatory intelligence. Collaborate with crossfunctional project teams [. .. ] and/or interns. Develop and implement regulatory operating guidelines and common work practices/ strategies within the team. Qualifications 1012 years of related work experience (Director candidates typically bring 12 years; Associate level candidates may be considered with 10 years and strong potential) , including 8 years in Regulatory Affairs CMC in the biotech/ pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus. Proven experience serving as a primary RACMC contact to health [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
Homeoffice möglich
[. .. ] verändern. Ist dies die Stelle, die Sie suchen? Wenn ja, lesen Sie weiter, um mehr zu erfahren, und bewerben Sie sich noch heute. Über die Stelle Wir [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] suchen einen Senior Regulatory Reporting Associate, der unser wachsendes Team verstärkt. Wenn du eine Leidenschaft für finanzielle und regulatorische Berichterstattung hast und echten Einfluss nehmen möchtest, bietet dir diese Position die Möglichkeit, von Anfang an Verantwortung zu übernehmen. Unser Regulatory Reporting Team sorgt für eine reibungslose Compliance und navigiert präzise und verantwortungsbewusst durch komplexe Meldeanforderungen. Du [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Senior Regulatory Lead, Switzerland Austria
A global biotech leader is seeking an
Associate Director, Local
Regulatory Lead for Switzerland and Austria. This hybrid role involves driving local regulatory strategy, managing interactions with Swissmedic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and AGES, and ensuring compliance across regulatory and quality operations. The ideal candidate has at least 8 years of experience in Regulatory Affairs within pharma/ biotech, a deep understanding of the regulatory environment, and excellent communication skills in both German and English. This position offers strategic influence in a fast-paced market. #J-18808-Ljbffr 72688367 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical
affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, [. .. ] to create a place where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and closeout visits (performed onsite or remotely) ensuring regulatory, ICHGCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding sitespecific actions; immediately communicates/ escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/ GCP [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Lead Risk Compliance Strategist (m/w/d)
• Zürich Zuerich
Führungs-/ Leitungspositionen Abgeschlossenes Studium
[. .. ] Sehr gutes Verständnis moderner Governance Strukturen und komplexer Organisationsprozesse Starke kommunikative Fähigkeiten sowie Routine im Umgang mit diversen Stakeholdergruppen Strukturierte, eigenständige Arbeitsweise kombiniert mit Moderationskompetenz und analytischer [...]
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[...] Stärke Seniority level Associate Employment type Fulltime Job function Business Development and Sales Industries Internet Publishing Referrals increase your chances of interviewing at Rocken by 2x #J-18808-Ljbffr 72687918 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Associate Director, Local
Regulatory Lead-Switzerland and Austria In this hybrid leadership role you drive local regulatory strategy and execution for Switzerland and Austria, translating global objectives into country-specific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] plans. You act as the regulatory partner to senior leadership, anticipate trends, and guide cross-functional teams to enable product launches and lifecycle submissions. [. .. ] and processes to ensure compliance and transparency Represent Global Regulatory Sciences in local cross-functional forums to shape priorities Lead cross-functional regulatory initiatives within the affiliate across Commercial, Medical Affairs, Market Access, Quality, and Supply Chain Build partnerships with external consultants, CROs, and industry stakeholders to advance regulatory objectives Monitor local legislation and regulatory guidance development as part of cross-industry associations (where assigned) University degree in life sciences, pharmacy, medicine or related field (MSc, Pharm D, MD) ; advanced degree [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Research Associate
• Hamburg
Veeda Lifesciences is seeking a Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] according to SOPs Conducts pre-study visits at potential investigational sites, to perform the study related feasibility and/or selection activities and evaluate their resources and facilities Collaborates with the Regulatory Affairs Department and concerned Clinical Operations staff for clinical submissions and contracts respectively for : Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome Preparation of study contracts relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Associate Director, Local Regulatory Lead-Switzerland and Austria
• Zug
Führungs-/ Leitungspositionen
Associate Director, Local
Regulatory Lead-Switzerland and Austria Join to apply for the Associate Director, Local Regulatory Lead-Switzerland and Austria role at Alnylam Pharmaceuticals The Associate Director, Local Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Lead Switzerland and Austria is a strategic leadership role with full accountability for national regulatory strategy, execution, and health authority engagement. This role serves [. .. ] Influence Represent Global Regulatory Sciences in strategic local crossfunctional forums, shaping priorities and aligning teams around shared goals Lead crossfunctional regulatory initiatives within the affiliate, integrating perspectives from Commercial, Medical Affairs, Market Access, Quality, and Supply Chain Build and maintain strong partnerships with external consultants, CROs, and industry stakeholders to advance regulatory objectives Represent Alnylam in local crossindustry associations (if assigned) , monitor and participate in shaping upcoming local legislation and regulatory guidance development Qualifications University degree in life sciences, pharmacy, [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Research Associate
• Dortmund, Nordrhein- Westfalen
Veeda Lifesciences is seeking a Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] according to SOPs Conducts pre-study visits at potential investigational sites, to perform the study related feasibility and/or selection activities and evaluate their resources and facilities Collaborates with the Regulatory Affairs Department and concerned Clinical Operations staff for clinical submissions and contracts respectively for : Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome Preparation of study contracts relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Leipzig, Sachsen
Veeda Lifesciences is seeking a Clinical Research
Associate (CRA) based in Germany for its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job Overview The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the [. .. ] according to SOPs Conducts pre-study visits at potential investigational sites, to perform the study related feasibility and/or selection activities and evaluate their resources and facilities Collaborates with the Regulatory Affairs Department and concerned Clinical Operations staff for clinical submissions and contracts respectively for : Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome Preparation of study contracts relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Associate Project Co-ordination Officer (S)
[. .. ] The Programming and Evaluation Support Unit (PESU) assists the Secretary General and the Chairpersonship in the implementation of the Organizations Project Management framework and standards, in line [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Common Regulatory Management System (CRMS) and with the recognised international standards. It is the primary point of contact for the Chairpersonship and participating States delegations on programmatic and project management matters in relation to the Unified Budget (UB) process, as well as the Extrabudgetary contributions. PESU advises senior management and field operations [. .. ] Secretariat, Vienna Issue Date: Aug 18, 2025 Closing Date: Jan 7, 2026 Employee Status: Fixed Term Schedule: Fulltime Education Level: Masters Degree (Secondlevel university degree or equivalent) Job Field: Political Affairs Target Start Date: As soon as possible Click the button below to visit the original announcement on the recruiting organizations website. #J-18808-Ljbffr 72577327 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Senior CRA Germany Therapeutic Area : Cell Gene Therapy Location : Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior Clinical Research
Associate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to join an innovative, fast-growing biopharmaceutical organisation advancing nextgeneration cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring highquality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative [. .. ] on track. Support feasibility assessments, site selection, initiation, routine monitoring, and closeout visits. Provide mentorship to junior CRAs and contribute to best practice development. Prepare study reports and maintain essential regulatory documentation. Partner with crossfunctional teams (Regulatory, Project Management, Data Management, Safety) . Contribute to inspection readiness and support regulatory audits as needed. Requirements 35+ years of independent monitoring experience as a CRA, with solid exposure to complex, interventional studies. Direct experience in cell gene therapy trials (e. g. , CART, [. .. ] 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including : Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. #J-18808-Ljbffr 72577882 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Strategic Regulatory Lead Switzerland Austria (Hybrid)
• Zug
Führungs-/ Leitungspositionen
A leading biotechnology company in Switzerland is seeking an
Associate Director, Local
Regulatory Lead. This pivotal role involves strategic leadership in national regulatory execution and health authority engagement. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The successful candidate will leverage a deep understanding of Swiss and EU regulations, drive cross-functional collaboration, and manage local regulatory submissions. This position offers a hybrid working model and is based in Zug, Switzerland. [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
CRA Germany or Austria-single-client
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 unique clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 with, but [. .. ] a place where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/ escalates serious issues to the project team and develops action plans. Maintains a working knowledge of [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
(Senior) Manager (m/w/d) Tax Compliance München
• München, Bayern
Abgeschlossenes Studium
[. .. ] internationalen und interdisziplinären Rolle einbringen. Sie wünschen sich ein dynamisches Umfeld, in dem Sie komplexe Fragestellungen im Bereich Tax Compliance bearbeiten und sich fachlich wie persönlich weiterentwickeln [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] können. Nicht jeder Associate, Counsel oder Partner ist in der aktuellen Kanzlei richtig positioniert oder vollends zufrieden und das wollen wir möglichst ändern. Wir führen Sie durch die spannendsten Optionen in Kanzleien, Boutiquen WPGs. Unser Kunde ist eine weltweit führende Beratungs- und Prüfungsgesellschaft, die sowohl national als auch international agiert und damit eine breite [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Senior Compliance Manager (m/f/d)
• München, Bayern
[. .. ] mutual, and appreciative feedback supporting individual development. Performancebased compensation and employerfinanced company pension benefits. Worklife balance, attractive family benefits, and a diverse company health management program. Additional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] information Seniority level: Associate Employment type: Fulltime Job function: Legal Industries: IT Services and IT Consulting Get notified about new Senior Compliance Manager jobs in Munich, Bavaria, Germany. #J-18808-Ljbffr 72448029 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Local Study Associate Director (LSAD) / Clinical Project Lead (m/w/d) Zelltherapie (Innendienst)
• Hamburg
Führungs-/ Leitungspositionen
Overview Local Study
Associate Director (LSAD) Cell Therapy (m/w/d) at Astra Zeneca. This role leads local study teams on country level and is responsible for the planful execution of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] defined components of clinical studies within allocated resources, budgets and timelines. The position ensures compliance with AZ procedural documents, international guidelines (ICH-GCP) [. .. ] Standortqualitätsrisikobewertungen durch und besucht Standorte, um Eignung und Risiken zu bewerten. Sorgt für fristgerechte Einreichung von Anträgen/ Dokumenten bei EC/ IRB zu Beginn und während der Studie; arbeitet mit der Regulatory Affairs-Abteilung zusammen. Sichert die rechtzeitige Erstellung des länderspezifischen Master-CSA (einschließlich Standortbudget) und notwendiger Änderungen; sorgt für relevante Übersetzungen und ICFs gemäß AZ-SOPs und lokalen Vorschriften. Stellt sicher, dass alle wesentlichen ICH-GCP-Dokumente auf Länder- und Standortebene vor Studienbeginn gesammelt und auf Richtigkeit überprüft sind. Plant und koordiniert [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Analyst-Model Audit
[. .. ] working on client sites. Significant opportunities for professional growth and development as we expand. Access to cutting-edge financial modelling tools and resources. Collaborative and supportive team culture [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Seniority level Associate Employment type Full-time Job function Other IT Services and IT Consulting #J-18808-Ljbffr 72366169 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Regulatory Affairs Associate pro Jahr?
Als Regulatory Affairs Associate verdient man zwischen EUR 50.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Regulatory Affairs Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 119 offene Stellenanzeigen für Regulatory Affairs Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Regulatory Affairs Associate Jobs?
Aktuell suchen 9 Unternehmen nach Bewerbern für Regulatory Affairs Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Regulatory Affairs Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Regulatory Affairs Associate Stellenangebote:
- Veeda Lifesciences (11 Jobs)
- Jazz Pharmaceuticals (3 Jobs)
- TRB Chemedica AG (2 Jobs)
- Syneos Health (1 Job)
- Gilead Sciences GmbH (1 Job)
In welchen Bundesländern werden die meisten Regulatory Affairs Associate Jobs angeboten?
Die meisten Stellenanzeigen für Regulatory Affairs Associate Jobs werden derzeit in Bayern (22 Jobs), Nordrhein-Westfalen (17 Jobs) und Sachsen (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Regulatory Affairs Associate Jobs?
Regulatory Affairs Associate Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
