Legal Investigator Stellenangebote


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16 Jobs für Legal Investigator


Stellenangebote Legal Investigator Jobs


Job vor 3 Tagen bei Jobleads gefunden

Lead Investigator (Global Compliance) (m/f/d)

• Düsseldorf, Nordrhein- Westfalen Duesseldorf Führungs-/ Leitungspositionen [. .. ] 31, 2025) totaled 9, 783.3 billion yen, with 618 consolidated subsidiaries and approximately 280, 000 employees worldwide. Visit us at What youll be doing Position requires a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] seasoned Lead Investigator to set and drive standards for corporate investigations across our worldwide businesses. While this role does not directly manage junior investigators, you will be instrumental in developing and delivering training programs for investigative teams across the global organization. You will also define the global standards by which all investigations are [. .. ] and you will play a key role in monitoring progress, ensuring timely outcomes, and reporting on investigation status. Key Responsibilities: Develop, implement, and enforce global investigation standards, ensuring alignment with legal and regulatory frameworks. Design and deliver training programs for junior investigators across the conglomerates diverse business units, ensuring consistency in investigative methods. Conduct follow-ups on ongoing investigations, ensuring timely resolution and tracking outstanding cases through to conclusion. Analyze investigation outcomes, identify trends, and report risks to senior leadership and [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden

Team Leader (Player/ Manager) Clinical Development Liaison (CDL) Neuromuscular Diseases-Germany

Führungs-/ Leitungspositionen Work-Life-Balance [. .. ] with insights from interactions with Investigators Email updates post-communication to internal ( CRO) stakeholders about outcomes of discussions Handover of interest/ knowledge about publication interest/ pub planning [...]
MEHR INFOS ZUM STELLENANGEBOT[...] or potential investigator Initiated Trials (IITs) Compliance Operate in a highly ethical manner and comply with all laws, regulations and policies. Complete mandatory training in assigned timelines upon hire as well as when new policies, SOPs, guidance are issued Team Leader Responsibilities Lead/coordinate the activities of small teams or individual field CDLs [. .. ] related to client projects in a timely and supportive way. Share relevant Amplity and Client procedures and processes to ensure team operate within a compliant framework and in accordance with legal requirements. Conduct regular field-visits and undertake regular 1:1s (face-to-face or remote, depending on geography) . Work closely with wider team and business to ensure key information and feedback is shared to improve future proposals and client offerings. Work in conjunction with People (HR) Team to process any [. .. ]

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Job vor 5 Tagen bei Jobleads gefunden

Medical Science Liaison Austria

[. .. ] Increase therapy awareness among prescribers and non-prescribers Manage the entire Austrian territory and all associated field activities Deliver medical training on Novocure products and disease areas Support [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and accompany investigator-sponsored trials (ISTs) and other research projects Provide HCP insights and market information to the company Participate in medical (Europe-wide) congresses, and organize and follow up on advisory boards Promote scientific advancement related to TT Fields Support Phase 3 studies in collaboration with clinical teams and researchers Build and [. .. ] (electric) also for private use Access to corporate benefits and employee discounts For this position, we offer an attractive stock package and compensation aligned with your qualifications and experience. For legal reasons, we note that the collective agreement minimum salary is 3, 682 gross per month. However, we are willing to offer a significantly higher salary. Our employees benefit from an attractive package of benefits, which may vary depending on position and area of deployment. #J-18808-Ljbffr 03438277 [. .. ]

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Job vor 7 Tagen bei Jobleads gefunden

Medical Science Liaison, Germany Dresden, Germany; Frankfurt, Germany; Kassel, Germany; Leipzig. . .

• Dresden, Leipzig, Frankfurt, Kassel, Sachsen, Hesse, Hessen [. .. ] as well as provide meaningful subject-matter expertise, to colleagues in Medical Affairs, Clinical Research, R D, Patient Advocacy and Commercial, while maintaining full compliance with all relevant [...]
MEHR INFOS ZUM STELLENANGEBOT[...] company, industry, legal, and regulatory requirements. This position reports to the Country Medical Affairs Director. What will you do? Identify key opinion leaders and cultivate a network of experts for disease areas of focus Respond to unsolicited requests and engage in meaningful, peer-to-peer scientific exchange of complex medical and scientific information [. .. ] country and define local dynamics related to patient diagnosis and referral for treatment Deliver medical/ scientific presentations to internal external stakeholders Assist with company-sponsored clinical trials and facilitation of investigator-initiated trials (ISTs) Lead planning and execution of regional advisory boards Collaborate with cross functional partners on internal projects and external initiatives Provide educational meeting support at scientific congresses Support training of cross functional teams Adhere to corporate and healthcare compliance guidance in all activities, including those related to clinical [. .. ]

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Job vor 9 Tagen bei Jobleads gefunden

Medical Science Liaison-Great Lakes

[. .. ] scientific expert Build and foster relationships with local, regional, and national KOLs and possibly Payers Effectively deliver medical/ clinical/ scientific presentations to a diverse external audience Support [...]
MEHR INFOS ZUM STELLENANGEBOT[...] clinical development activities, investigator recruitment and education Development and execution of their Territory Management Plan (TMP) that is aligned with the overall Medical Goals and Plan Contribute to developing metrics, qualitative and quantitative MSL reports, SOPs/ Business Practices for the MSL function Responding to unsolicited medical information requests submitted by SRRK field teams (eg. [. .. ] exchange to unsolicited questions at SRRK medical booths at congresses May respond to and document unsolicited requests for scientific information Conduct all activities and responsibilities in accordance with all relevant legal, regulatory and corporate regulations and guidelines, including the Scholar Rock Business Conduct Ethics, policies and procedures Candidate Requirements MD, Pharm D, or Ph D preferred. Advanced professional degree (NP, PT etc) may be considered for candidates with significant clinical neuromuscular disease experience Neurology and/or rare disease experience with prior launch experience [. .. ]

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Job vor 11 Tagen bei Jobleads gefunden

(Senior) Investigator/ (Senior) Investigation Lawyer (m/f/d) at Allianz SE

• München, Bayern [. .. ] role holder will help shape how the function adopts investigative technology and AI pragmatically, and in a responsible, human-led way. We welcome candidates from an investigations, IT-forensics [...]
MEHR INFOS ZUM STELLENANGEBOT[...] or legal-tech background who combine strong investigative capability with a genuine interest in developing this area. Who will you join? Group Compliance Investigations About The Role Allianz Group Compliance is evolving its investigations function toward a more integrated, increasingly technology-and AI-enabled operating model. We are at the beginning of [. .. ] of the insurance business is an advantage Some practical, operational experience with investigative technology e. g. e-discovery, data analytics, IT forensics or legal-tech tools whether gained as an investigator, IT-forensics specialist or legal-technology professional Interest in helping build an AI-enabled investigation capability, with a pragmatic and responsible view of where technology adds real value; Strong communication and report-writing skills (fluent English required; additional languages a plus) Results-driven team player Willingness to work across time [. .. ]

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Job am 09.09.2026 bei Jobleads gefunden

Associate Director, Medical Science Liaison (MSL) , Neurology (Southeast)

Führungs-/ Leitungspositionen [. .. ] stakeholder needs with available Zenas resources. Demonstrate proficiency in delivering educational resources and clinical information in response to an established need/request. Liaise with investigators to support clinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] research activities (investigator-initiated and company sponsored) . Facilitate speaker development and training. Engage in timely and fair-balanced scientific exchanges with HCPs in a compliant, ethical manner in response to unsolicited requests for information related to Zenas products. Lead, contribute to, attend, and provide scientific support at international, national, regional, and local [. .. ] and managing and resolving conflict Excellent communication skills (written, verbal, listening, and presentation) Results-oriented Team oriented Proven track record of success Current knowledge full understanding of all relevant industry, legal, and regulatory compliance guidelines Commitment to the highest ethical, legal, regulatory, and scientific standards The ideal candidate will live in FL, TN, or GA Zenas is committed to fair and equitable compensation practices. The base salary pay range for this role is 181, 600 to 227, 000. Actual compensation packages [. .. ]

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Job am 06.09.2026 bei Jobleads gefunden

Senior Site Contracts Associate, IQVIA Biotech-Germany

• Frankfurt, Hesse Beratungs-/ Consultingtätigkeiten [. .. ] position may also include linemanagement responsibilities. If you are a strategic thinker with strong expertise in international clinical trial contracting, wed love to speak with you. Key [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Responsibilities Develop complex investigator grant estimates, contracting strategies, and proposal text to support business development. Create and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multiprotocol programs. Collaborate closely with sponsors, stakeholders, and RSU regional teams to ensure successful delivery of the project scope and compliance with sponsor requirements. Provide legal, operational, and financial contracting expertise to support site agreements and facilitate efficient study startup and maintenance. Create and review scientific, technical, and administrative documentation required for study initiation. Assess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company. Ensure contracting efficiency, adherence to [. .. ]

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Job am 04.09.2026 bei Jobleads gefunden (Senior) Investigator/ (Senior) Investigation Lawyer (m/f/d) at Allianz SE • München, Bayern [. .. ] and regulations Preferred Qualifications In-depth knowledge of the insurance business is an advantage Some practical, operational experience with investigative technology-e. g. e-discovery, data analytics, IT forensics or [...]
MEHR INFOS ZUM STELLENANGEBOT[...] legal-tech tools-whether gained as an investigator, IT-forensics specialist or legal-technology professional Interest in helping build an AI-enabled investigation capability, with a pragmatic and responsible view of where technology adds real value; Strong communication and report-writing skills (fluent English required; additional languages a plus) Results-driven team player Willingness to work across time [. .. ]

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Job am 31.08.2026 bei Jobleads gefunden

Medical Science Liaison/ Sr. Medical Science Liaison

• Hamburg [. .. ] various activities locally and regionally. Provide local and regional feedback to HQ when performing Business Development Due Diligence. Deliver inputs to head office led medical programs ahead [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of launch. Coordinate Investigator Sponsored Studies (ISSs) as appropriate and support studies on the local level Coordinate medical information enquiries in collaboration with MA/ SMA and HQ in Stockholm. Attend relevant local, regional and global congresses and symposia to represent Sobi and interact with appropriate stakeholders and customers. Represent the scientific interests in internal [. .. ] Governmental Organizations within the therapeutic area. Maintain and develop strong relationships with scientific societies and central decision makers Provide advice to the organization and management on medical matters and their legal implications. Safeguard that the medical and scientific knowledge for the therapeutic area remains at the forefront of contemporary thinking; remain updated on therapeutic trends related to new and existing products. Qualifications Education/ Learning Experience/ Work Experience Required: University degree in medical/ science or other relevant field +3 years of direct [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Medical Scientific Affairs Lead (m/f/d) Western Europe • Köln, Nordrhein- Westfalen Führungs-/ Leitungspositionen [. .. ] Review and approve promotional and nonpromotional medical content in accordance with healthcare systems regulations in the West Europe Region. Clinical Evidence Real World Data Lead regional evidence [...]
MEHR INFOS ZUM STELLENANGEBOT[...] generation activities, including investigator-initiated studies, realworld evidence programs, and clinical collaborations. Oversee regional evidence generation priorities and ensure alignment with EMEA medical objectives. Analyze and communicate scientific data to internal and external stakeholders. Ensure medical insight collection and feedback into global development teams. Compliance Governance Ensure all medical activities comply with internal policies, industry standards, French regulations (DMOS, ANSM) , and ethical guidelines. Support the legal and regulatory review of scientific materials. Your Qualification : Advanced degree in Medicine, Pharmacy, Biology, or related life sciences (MD, Pharm D, Ph D preferred) . Strong background in infectious diseases and/or clinical microbiology. Minimum of 10 years of professional experience in diagnostics, medical devices or pharmaceutical industry. Minimum of 5 [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Legal Officer-Middle East Programme • Genf Founded in 2013, Legal Action Worldwide is an independent nonprofit organisation comprised of human rights lawyers and jurists, united in our belief that those who have experienced grave human [...]
MEHR INFOS ZUM STELLENANGEBOT[...] rights violations and international crimes, should receive targeted, survivorcentred, gendercompetent, and traumainformed support to access the justice they deserve. LAWs teams work in/ on conflictaffected [. .. ] 4 years demonstrated experience in litigating human rights, humanitarian law, or international criminal law. Minimum of 4 years demonstrated experience investigating human rights violations or international crimes. Experience as an investigator within an international tribunal or mechanism is desirable. Strong understanding of gender perspectives in armed conflict and fragile security contexts. Demonstrated experience working with partners on litigation initiatives. Experience in case preparation and development, including investigation, case strategy, legal drafting to an excellent standard. Proficient in MS Office packages (Excel, [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Senior Medical Director, Global Risk Management Safety Surveillance • Morges, Waadt Führungs-/ Leitungspositionen [. .. ] latephase drug development candidates and marketed products in conjunction with Clinical Development, Medical Writing, Statistics, and Regulatory Affairs. Drive the safety strategy for Reference Safety Information for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Incyte products, including Investigator Brochures and new or updated labeling (USPI, Sm PC, or CDS) for marketed products in the context of multidisciplinary groups within Incyte or joint committees between external partners. Participate in internal safety process improvements and updates, including new means of effective presentation of early phase clinical study status reports with regard [. .. ] revise standard communications that include specific adverse event information. Champion risk management safety strategy to internal (eg, Clinical Development, Medical Affairs, Regulatory Affairs, Quality Assurance, Commercial, Translational Experimental Medicine and Legal) and external (eg, regulators and commercial collaborators) stakeholders. Serve as the GRMSS medical representative for joint clinical development programs with external partners as required. Other responsibilities, as necessary. In the absence of the EU/ UK QPPV, the GRMSS physician (or their designated backup) is responsible for responding to productrelated queries [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Senior Medical Director-Executive Medical Director, Global Risk Management Safety Surveillance • Morges, Waadt Führungs-/ Leitungspositionen [. .. ] phase drug development candidates and marketed products in conjunction with Clinical Development, Medical Writing, Statistics, and Regulatory Affairs. Drive the safety strategy for Reference Safety Information for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Incyte products, including Investigator Brochures and new or updated labeling (USPI, Sm PC or CDS) for marketed products in the context of multidisciplinary groups within Incyte or joint committees between external partners. Participate in internal safety process improvements and updates, including new means of effective presentation of early phase clinical study status reports with regard [. .. ] revise standard communications that include specific adverse event information. Champion risk management safety strategy to internal (eg, Clinical Development, Medical Affairs, Regulatory Affairs, Quality Assurance, Commercial, Translational Experimental Medicine and Legal) and external (eg, regulators and commercial collaborators) stakeholders. Serve as the GRMSS medical representative for joint clinical development programs with external partners as required. In the absence of the EU/ UK QPPV, the GRMSS physician (or their back-up) is responsible for responding to product-related queries as delegated by [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Medical Scientific Affairs Lead (m/f/d) Western Europe • Köln, Nordrhein- Westfalen Führungs-/ Leitungspositionen [. .. ] Review and approve promotional and nonpromotional medical content in accordance with healthcare systems regulations in the West Europe Region. Clinical Evidence Real-World Data Lead regional evidence generation [...]
MEHR INFOS ZUM STELLENANGEBOT[...] activities, including investigator-initiated studies, real-World evidence programs, and clinical collaborations. Oversee regional evidence generation priorities and ensure alignment with EMEA medical objectives. Analyze and communicate scientific data to internal and external stakeholders. Ensure medical insight collection and feedback into global development teams. Compliance Governance Ensure all medical activities comply with internal policies, industry standards, French regulations (DMOS, ANSM) , and ethical guidelines. Support the legal and regulatory review of scientific materials. Your Qualification: Advanced degree in Medicine, Pharmacy, Biology, or related life sciences (MD, Pharm D, Ph D preferred) . Strong background in infectious diseases and/or clinical microbiology. Minimum of 10 years of professional experience in diagnostics, medical devices or pharmaceutical industry. Minimum of 5 years [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden Medical Scientific Affairs Lead (m/f/d) Western Europe Führungs-/ Leitungspositionen [. .. ] Review and approve promotional and nonpromotional medical content in accordance with healthcare systems regulations in the West Europe Region. Clinical Evidence Real World Data Lead regional evidence [...]
MEHR INFOS ZUM STELLENANGEBOT[...] generation activities, including investigator-initiated studies, realworld evidence programs, and clinical collaborations. Oversee regional evidence generation priorities and ensure alignment with EMEA medical objectives. Analyze and communicate scientific data to internal and external stakeholders. Ensure medical insight collection and feedback into global development teams. Compliance Governance Ensure all medical activities comply with internal policies, industry standards, French regulations (DMOS, ANSM) , and ethical guidelines. Support the legal and regulatory review of scientific materials. Your Qualification Advanced degree in Medicine, Pharmacy, Biology, or related life sciences (MD, Pharm D, Ph D preferred) . Strong background in infectious diseases and/or clinical microbiology. Minimum of 10 years of professional experience in diagnostics, medical devices or pharmaceutical industry. Minimum of 5 years [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Legal Investigator pro Jahr?

Als Legal Investigator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Legal Investigator Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 16 offene Stellenanzeigen für Legal Investigator Jobs.


In welchen Bundesländern werden die meisten Legal Investigator Jobs angeboten?

Die meisten Stellenanzeigen für Legal Investigator Jobs werden derzeit in Nordrhein-Westfalen (3 Jobs), Bayern (2 Jobs) und Sachsen (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Legal Investigator Jobs?

Legal Investigator Jobs gehören zum Berufsfeld Rechtswesen, Justiz und Verwaltung.


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Dauer: 0.0422 s., Vers. V.2025-d-2007-Ind-141