192 Jobs für Compliance Investigator
Stellenangebote Compliance Investigator Jobs
Job vor 8 Tagen bei Mindmatch.ai gefunden
Randstad Belgium
• Berlin, BE
Angebote von Zeitarbeitsunternehmen
[. .. ] you will play a pivotal role in driving the success of clinical trials within the medical device sector. You will serve as the primary link between the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sponsor and various investigator sites. This is a highly flexible freelance project with an average monthly resource requirement ranging from 50 to 100 of a full-time position. We welcome applicants with differing availabilities, as we may onboard two freelancers to share the project scope. Your day-to-day operations will be fully supported [. .. ] Monitoring Visits, and Close-out Visits. Regional Travel On-Site Presence: Execute required on-site monitoring activities and hospital visits, which are primarily situated across central, northern, and western Germany. Compliance Training: Actively participate in sponsor training and ensure all clinical trial activities strictly adhere to protocols, regulatory guidelines, and quality standards. Reporting: Deliver clear, ad-hoc, and scheduled updates via email, telephone calls, and meetings to Clinical Trial Leaders. 03140815 [. .. ]
Job am 07.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Cologne, NW
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
• Munich, BY
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
Clinical Scientist
• Frankfurt
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
• Düsseldorf, NW
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Leipzig, SN
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
• Frankfurt
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Berlin, BE
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
Clinical Scientist
• Leipzig, SN
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Dortmund, NW
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Munich, BY
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
Clinical Scientist
• Düsseldorf, NW
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
Clinical Scientist
• Berlin, BE
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
Clinical Scientist
• Hamburg, HH
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Meet Life Sciences
• Frankfurt
[. .. ] global priorities. What youll do Define and execute the global medical strategy aligned to business objectives Provide medical leadership across global, cross-functional stakeholders Drive evidence generation (Phase [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] IV, RWE, investigator-initiated studies) Lead scientific exchange via congresses, advisory boards, and expert engagement Build trusted relationships with KOLs, academic partners, and patient communities Oversee publication planning and scientific communications Deliver global medical education and training initiatives Review/approve medical content and materials Gather insights to continuously refine strategy and priorities Ensure compliance with all relevant regulations, policies, and quality standards What were looking for MD, Ph D, Pharm D or equivalent advanced scientific degree Proven expertise in the creation and execution of Medical Affairs strategy within the Pharmaceutical/ Biotech industry (3+ Years experience in a Lead function) Experience in Neurology/ Movement Disorders Clear, confident [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Leipzig, SN
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Berlin, BE
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Hamburg, HH
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Cologne, NW
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Hamburg, HH
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Stuttgart, BW
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Pentixapharm AG
Clinical Scientist
• Dortmund, NW
[. .. ] data review and regulatory submissions. The role will also include scientific site management support to ensure high-quality execution of imaging procedures and consistent implementation of study-specific requirements [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across investigator sites. The clinical scientist will conduct in-depth literature, data and expert research to support key decision-making in the clinical program. Working closely with cross-functional colleagues, the Clinical Scientist will contribute directly to advancing Pentixa For/ Pentixa Ther and our broader pipeline toward registration. Your Tasks Support and independently execute Phase 13 radiopharmaceutical and oncology clinical trials including protocol development, site initiation support, scientific oversight of study conduct, and ensuring GCP compliance in close collaboration with Clinical Operations and CROs Serve as day-to-day scientific/ clinical contact for investigator sites, CROs, and external partners Contribute to and author clinical study protocols, protocol amendments, investigator brochure updates, Clinical Study Reports (CSRs) , and regulatory submission documents In-depth research of clinical and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Düsseldorf, NW
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Essen, NW
[. .. ] A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or an investigator facing role (e. g. , clinical project manager, 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 should have a solid understanding of scientific exchange in the context of a compliance landscape. Fluency in English and in local language in country of 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 [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Frankfurt
[. .. ] including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/ study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Compliance Investigator pro Jahr?
Als Compliance Investigator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Compliance Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 192 offene Stellenanzeigen für Compliance Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Compliance Investigator Jobs?
Aktuell suchen 14 Unternehmen nach Bewerbern für Compliance Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Compliance Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Compliance Investigator Stellenangebote:
- Tigermed (28 Jobs)
- Pentixapharm AG (11 Jobs)
- Meet Life Sciences (7 Jobs)
- Randstad Belgium (1 Job)
- Bristol Myers Squibb EU Policy (1 Job)
In welchen Bundesländern werden die meisten Compliance Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Compliance Investigator Jobs werden derzeit in Nordrhein-Westfalen (25 Jobs), Bayern (17 Jobs) und Baden-Württemberg (15 Jobs) angeboten.
Zu welchem Berufsfeld gehören Compliance Investigator Jobs?
Compliance Investigator Jobs gehören zum Berufsfeld Compliance & Datenschutz.
