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29 Jobs für Regulatory Affairs Coordinator


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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC)

Site Engagement Manager, Immunology (Germany)

• Leipzig, SN [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Frankfurt [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Berlin, BE [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Dortmund, NW [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Munich, BY [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Cologne, NW [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Hamburg, HH [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Düsseldorf, NW [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Essen, NW [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Risk Governance Manager-Vice President • Frankfurt, Hesse Führungs-/ Leitungspositionen [. .. ] and procedures. The role will have direct exposure to Senior Management and cross-functional to Finance, Front Office and other functions to ensure a consistent roll out of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the framework. Regulatory Monitoring and Change Management: Responsible for ensuring that German risk related regulations are understood and adhered to; provide oversight of local Risk projects and liaise with the Global Change function and local counterparts in Compliance, Finance and other Functions as required for the respective project. Outsourcing Controls: Monitoring and enhancement of the SLA for Risk with other Nomura entities, escalating in cases of breaches of the terms. Operational Risk Coordinator for the Risk Function including controls testing. Regulatory Liaison: Managing the relationship with the German regulators for risk related matters. Risk MI: Management of consolidated Risk MI for the entity, liaising with the global reporting teams who are responsible for the production of the reports. Production of ad-hoc reports [. .. ]

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Job gestern bei Jobleads gefunden

Regulatory Affairs Executive

Salary: Competitive Job Timings: 8 AM to 5 PM Requirements: Graduation in pharmacy background or any relevant degree. About the role: To contribute to the regulatory documents and reports [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to be included in regulatory submission. Documents and track regulatory submission and regulatory authority license approval for EU market and most probably Germany. Provide regulatory support to the teams and associates of the company. Responsibilities: Application for new registration to receive license from EMA. Cooperation with authorities [. .. ] and receipt of approval from MAH. Maintenance of existing approvals and maintaining formats and content review of packaging texts, Sm PC, PIL and labelling. Review task for, support and mentor Regulatory Affairs associates. Provide on-going regulatory support to the regulatory affairs team lead and to project teams to ensure regulatory concerns are planned and accounted for the relevant data are generated to meet project objectives. Provide format and contents review of packaging texts, Summary of Product Characteristics, Patient Information Leaflet and labelling. Contribute to data entry in softwares, Control that invoicing is correctly done. Assist the RA platform or hub leader or Coordinator in presales. Candidate Requirements: Masters or higher graduate degree in a science related field. Strong coordination skills and leadership. Excellent organizational and interpersonal skills. confident use of MS Office and Multi-tasking. Effective oral and written communicational skills. Proactive attitude and able to work on own initiative as well as [. .. ]

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Job vor 9 Tagen bei Jobleads gefunden Contract Management Lead (Procurement) Führungs-/ Leitungspositionen [. .. ] led contracting help deska new capability designed to scale contract drafting, review, negotiation, and lifecycle management without significantly increasing headcount. You will own the service strategy, operating [...]
MEHR INFOS ZUM STELLENANGEBOT[...] model, delivery oversight, coordinator enablement, workflow design, and performance tracking. Sourcing coordinators will manage day-to-day negotiations and agreement execution; you will ensure they have the tools, playbooks, training, guidance, and escalation support required to deliver timely, consistent, and well-governed outcomes. This is a builder-operator and service-ownership role for someone [. .. ]

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Job am 06.09.2026 bei Jobleads gefunden

Building Regulations Permitting Specialist

• München, Bayern [. .. ] IMPACT You own Proxima Fusions building regulations and permitting strategy-across multiple sites, from day one. Your work spans the Alpha facility permitting process, site development approvals, and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the early regulatory landscape definition for Stellaris-a programme horizon broad enough that you will be shaping permitting strategy for projects still being defined alongside those already in motion. Permitting is a critical path item, not a support function. You ensure that regulatory requirements are understood early and fed upstream into design and [. .. ] systems design decisions, and you engage with engineers upstream rather than reviewing outputs downstream Experienced managing authority relationships directly-you are the owner-side face to planning bodies, not a coordinator of external consultants who hold those relationships Aware of the radiation protection licensing landscape in Germany-you do not need to be a specialist, but you understand how nuclear or radiation-related facility licensing timelines interact with building permit sequencing and can plan accordingly Fluent in German and English, written [. .. ] are German-language; internal working language is English Familiar with AI tools and digital working methods; comfortable in a lean, high-autonomy environment Background in planning, building regulations, or regulatory affairs for energy, industrial, or research facilities is strongly preferred; experience across multiple simultaneous permitting processes is a strong plus Aware of the radiation protection and nuclear licensing landscape in Germany is a plus-you do not need to be a specialist, but you understand how licensing timelines interact with building [. .. ]

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Job am 05.09.2026 bei Jobleads gefunden Medical Affairs Research Coordinator (m/w/d) • Frankfurt, Hesse Medical Affairs Research Coordinator (m/w/d) Verantwortungsbereich: Koordination der von Medical Affairs initiierten und/oder unterstützten Forschungsprojekte (nicht-interventionelle Studien, Register o. ä. ) einschließlich Projekt- und Budget Tracking. Erstellung und Aktualisierung [...]
MEHR INFOS ZUM STELLENANGEBOT[...] von Präsentationen. Verwalten von Beschaffungs-, Buchhaltungs- und Rückstellungsprozessen. Zusammenstellen und Überprüfen von Daten sowie Integration in vorformatierte Berichte. Interaktionen mit [. .. ]

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Job am 04.09.2026 bei Jobleads gefunden

Medical Affairs Research Coordinator (m/w/d)

• Frankfurt, Hesse [. .. ] Menschen auf der ganzen Welt zu verbessern. Unsere Geschäftsbereiche entwickeln, produzieren und vermarkten innovative Arzneimittel, Lösungen und Dienstleistungen in mehr als 100 Ländern und Regionen. Verantwortungsbereich: Koordination [...]
MEHR INFOS ZUM STELLENANGEBOT[...] der von Medical Affairs initiierten und/oder unterstützten Forschungsprojekte (nicht-interventionelle Studien, Register o. ä. ) einschließlich Projekt- und Budget Tracking. Erstellung und Aktualisierung von Präsentationen. Verwalten von Beschaffungs-, Buchhaltungs- und Rückstellungsprozessen. Zusammenstellen und Überprüfen von Daten sowie Integration in vorformatierte Berichte. Interaktionen mit Studienzentren und ggf. Besuche in Deutschland. Koordination von Aktivitäten [. .. ]

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Job am 24.08.2026 bei Jobleads gefunden Senior Compliance Risk Manager • Wien [. .. ] Risk Management (TPRM) , ICT risk management, and Business Continuity Management (BCM) . You will ensure that our governance, processes, and controls comply with Mi CAR, DORA, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] EU GDPR, and Austrian regulatory expectations while supporting strong cross-functional collaboration. In this role, you will manage due diligence and oversight of external service providers, maintain the ICT risk framework and central risk register, coordinate BCM and Disaster Recovery activities, support incident and vendor monitoring, and prepare clear reporting for the Head of Risk, [. .. ] risk management frameworks and regulatory expectations (e. g. , DORA operational resilience requirements) . Monitor continuity risks, gaps, and readiness; track remediation of continuity-related findings. Serve as a central coordinator during disruptions or crisis management events, working with Business, IT, CISO, and leadership teams. Promote awareness and training on business continuity roles, responsibilities, and procedures across the organisation. What Makes You Special You hold a university degree in Law, Economics, Finance, Business, IT Risk, or a related field You bring [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden

Medical Affairs Coordinator

• München, Bayern [. .. ] individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description Your responsibilities will involve: Providingadministrative [...]
MEHR INFOS ZUM STELLENANGEBOT[...] support to Medical Affairs department Preparingintradepartmental announcements, newsletters, departmental surveys, and presentations Maintainingdepartmental tracking and metrics tools Coordinatingdepartmental onboarding and induction training of hired, promoted, or contracted Medical Affairs staff Developingreports for Medical Affairs management Maintaining Medical Affairs knowledge libraries Trackingtraining compliance of Medical Affairs staff and ensuring resolution of issues Qualifications Qualifications and [. .. ]

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Job am 06.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Stuttgart [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Berlin [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Düsseldorf [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Düsseldorf [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Cologne [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Stuttgart [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Hamburg [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Frankfurt [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ] residence required. Demonstrates a proactive nature to engage and motivate investigators/ clinical trial sites. Excellent oral and written communication skills and interpersonal skills Knowledge of FDA compliance, GCP guidance and regulatory requirements Ability to manage a geographically assigned territory from a home-based office. Willingness to travel within the assigned region is required, 50 or more; overnight travel is required as needed. Computer skills including Excel, Word, Power Point, Outlook, and programs such as Live Meeting, Zoom and MS Teams are [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Regulatory Affairs Coordinator pro Jahr?

Als Regulatory Affairs Coordinator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Regulatory Affairs Coordinator Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 29 offene Stellenanzeigen für Regulatory Affairs Coordinator Jobs.


In welchen Bundesländern werden die meisten Regulatory Affairs Coordinator Jobs angeboten?

Die meisten Stellenanzeigen für Regulatory Affairs Coordinator Jobs werden derzeit in Nordrhein-Westfalen (6 Jobs), Bayern (2 Jobs) und Baden-Württemberg (2 Jobs) angeboten.


Zu welchem Berufsfeld gehören Regulatory Affairs Coordinator Jobs?

Regulatory Affairs Coordinator Jobs gehören zum Berufsfeld Regulatory Affairs & Management.


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