32 Jobs für Legal Investigator
Stellenangebote Legal Investigator Jobs
Job am 06.03.2026 bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
[. .. ] selection activities. Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites. Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/ investigator is needed. Qualifications University/ college degree (Md/Pharm D degree) , or an equivalent combination of education, training and experience. On-site monitoring experience is a plus. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Demonstrated ability to work in a dynamic environment, under compressed deadlines [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
Contract Negotiator 2-FSP-German speaker
• AT- 9 Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget templates [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] procedures (SOPs) , and regulatory requirements. With deep medical expertise, this role serves as the primary authority on medical issuesproviding clear, informed guidance and answering complex questions [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
Medical Science Liaison Complement-Mediated Diseases
• München, Bayern
[. .. ] 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 Accredited doctorate degree in a life-science or basic-science discipline (Pharm. D. , D. Sc. , D. N. [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Zug
[. .. ] life practice to meet customer needs. Presents data and information in a manner appropriate to the audience and request. Execute plans regarding reactive and proactive outreaches as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] approved via the legal/ HCC exceptions process. Integrates scientific data into real life practice to meet customer/ audience needs, adapting interpersonal style to particular situations and people. Anticipates the responses of various individuals and teams based on their vantage point and perspective. Prioritize franchise customer-based initiatives and field responsibilities, while balancing administrative duties and project responsibilities. Leverages knowledge of standards of care and Janssen company/ investigator sponsored clinical trials and competitor landscape to facilitate external-internal research communication. Engages with external investigators regarding unsolicited research inquiries and act as liaison to R D, Medical Affairs and operations teams. Provides clinical trial support to identify potential sites, resolve issues with enrolled sites, and participate in meetings as [. .. ]
Job gestern bei Jobleads gefunden
Director, MEG Lead Oncology, Medical Evidence Generation
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] Evidence Generation (MEG) Lead in Oncology at Bristol Myers Squibb oversees evidence generation for the Oncology portfolio, including Clinical Research Collaborations (CRCs) , Medical Affairs Sponsored Studies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (MAST) , and Investigator-Sponsored Research Studies (ISRs) , ensuring alignment with internal strategies to accelerate pipeline development. Key responsibilities include fostering relationships with thought leaders, managing the lifecycle of CRCs and ISRs, and addressing evidence gaps by partnering with academic and professional networks. Responsibilities will include, but are not limited to, the following [. .. ] . Financial Well-being and Protection 401 (k) plan, short-and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work-life benefits include Paid Time Off US Exempt Employees flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees 160 hours [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Berlin
[. .. ] and budgets specialist to join our team in Germany. In this role you will be responsible for direct site facing contract and budget negotiations through contract execution [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (p CRO) and collaborating with other lines to plan site contracting timelines though start up. Key Accountabilities Exercise good judgment in balancing the risks to the sponsor in making budget and contractual decisions against the impacts to client clinical trial timelines. [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Associate Director, Audit Strategy and Vendor Quality
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] personal lives. Read more: careers. bms. com/working-with-us. R D Quality, Audit Strategy Operationalize and execute the riskbased audit and quality strategy across Therapeutic Areas, R D processes, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] investigator sites, vendors, and digital health aligned with ICH E6 (R3) , regulatory expectations, and company objectives. Lead the planning, conduct, and reporting of audits and assessments, ensuring consistency, quality, and timely delivery, in partnership with Clinical Auditing team, Development Quality and business stakeholders. Identify, assess, and elevate quality risks, contributing [. .. ] Programs (EAP) . Financial Wellbeing and Protection: 401 (k) plan, short and longterm disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support and survivor support. Worklife Benefits Include US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) ) . Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non Exempt, Hourly Employees: 160 hours annual paid [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
Site Identification Specialist
• Wien
[. .. ] selection activities. Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites. Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/ investigator is needed. Qualifications University/ college degree (Md/Pharm D degree) , or an equivalent combination of education, training and experience. On-site monitoring experience is a plus. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Demonstrated ability to work in a dynamic environment, under compressed deadlines [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
(Senior) Medical Manager Dermatology (m/f/d)
• München, Bayern
[. .. ] as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-house training for MSLs, [. .. ] national and international level Contributes positively to a strong culture of business integrity and ethics and embraces the Mission, Vision and Values of the organization Acts within compliance, regulatory and legal requirements as well as within company guidelines Requirements Relevant scientific degree (medicine, life sciences or equivalent) , MD or Ph D preferred 3-5 years medical affairs experience in the pharmaceutical industry Experience in Dermatology/ Immunology (preferred) and understanding of customer-and market needs Launch expertise within the companys key therapeutic [. .. ]
Job am 27.02.2026 bei Jobleads gefunden
[. .. ] 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. We look forward to receiving your application. More information about Novocure and our therapy can be found on our website at. Our employees benefit from [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Contract Negotiator 2-FSP-German speaker
• Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] templates as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report [. .. ]
Job am 17.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] speaker page is loaded # # Contract Negotiator 2-FSP-German speakerlocations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob requisition id: R1527752Essential Functions Develop Coordinate the development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget templates as required as applicable to the position Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements Report [. .. ]
Job am 17.02.2026 bei Jobleads gefunden
Contract Negotiator 2-FSP-German speaker
• Frankfurt, Hesse
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] templates as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report [. .. ]
Job am 15.02.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] procedures. Ensure timely and informative scientific/ medical exchanges with external customers and internal partners, which accurately reflect scientific data, in accordance with compliance policies and procedures as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] well as with legal and ethical standards. Coordinate the timely and appropriate response to internal and external Medical Information enquiries in your region, utilizing global medical information resources and in line with local regulatory requirements. Drive the identification, development and alignment with Key Opinion Leaders, other important customers and stakeholders, including professional organizations. Deliver [. .. ] relationship with all functions in country, including commercial operations, sales and marketing teams. Identify and implement appropriate high-impact medical research projects to support the business objectives, including Alexionsponsored and investigator-initiated projects. Support the implementation of the local publication plan, aligned with local and Global strategy and in conjunction within country functions and EMEAC medical Affairs team, to ensure widespread data dissemination and local data generation, including congress abstracts, publications, case studies. Attend appropriate national and international meetings and congresses [. .. ]
Job am 12.02.2026 bei Jobleads gefunden
Study Physician sponsor dedicated in Germany
• München, Bayern
[. .. ] Typical candidates have 1015 years of working experience (clinical practice +/-industry) post residency/ fellowship. Its not necessary that they are licensed in US or a specific country [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (check local legal requirements) . Preferred if completed fellowship, residency or specialization in internal medicine, oncology, neurology, immuneoncology, cardiology, pediatrics, or emergency medicine. Experience Preferences Medical Monitoring Experience Preferred Pharma company experience preferred, but CRO experience is fine. Pharma Company Experience Preferred; however, CRO experience is fine. If no industry experience, clinical practice should include work as principal investigator/ subinvestigator in clinical trials for a reasonable amount of time. Key skill areas: clinical trial protocol writing/ reviewing, identifying medically relevant critical data, medical risks, risk mitigation/ monitoring plan, medical quality review, clinical quality monitoring, review of medical data/ lists, plausibility checks, patient profile review, trial documents review (informed consent, [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
[. .. ] e. , dermatologists) . Systematically generate, prioritize and communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for [. .. ] and investigators. Provide medical/ scientific leadership and expertise to internal and external groups Conduct internal trainings on medically relevant topics. Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory requirements and guidelines governing scientific interactions with physicians and healthcare professionals across all activities. Share best practice experiences with fellow MSLs. Embrace and demonstrate the Incyte Corporate Values. Contribute positively to a strong culture of business integrity and ethics. Employees assigned to this job are not intended to [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
Medical Science Liaison Dermatology (m/f/d) - Frankfurt, Kassel, Saarbrücken
[. .. ] (i. e. dermatologists) . Systematically generate, prioritize and communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for [. .. ] and investigators. Provide medical/ scientific leadership and expertise to internal and external groups Conduct internal trainings on medically relevant topics. Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory requirements and guidelines governing scientific interactions with physicians and healthcare professionals across all activities. Share best practice experiences with fellow MSLs. Embrace and demonstrate the Incyte Corporate Values. Contribute positively to a strong culture of business integrity and ethics. Employees assigned to this job. They are not intended [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] VDC consistent with such position. The role of Senior EH S Manager is key to ensuring that VDC complies with its EH S statutory obligations (i. e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] , Region specific legal and statutory regulations, codes of practice) , customer requirements and industry best practice for the designated project/ s. The Senior EH S manager will provide strategic direction, leadership, and management to the VDC Project EHS Manager, EHS Advisor and contractor/ s (i. e. , where applicable) on VDC EH S [. .. ] reports etc. ) for submission by the 2 nd day of next month. Contribute to the enhancement of the environmental aspects and impacts program across EMEA. Lead incident and accident investigator for recordable incidents or accidents for your designated projects. Participate in customer meetings (i. e. , biweekly progress meetings, incident close-out meetings) and walks where required. Participate in bi-annual EHS Safety Management System Reviews to take account of lessons learnt, customer requirements and best practices. Lead EH S [. .. ]
Job am 28.12.2025 bei Jobleads gefunden
Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] is responsible for working with the physicians within Clinical to provide clinical research support for programs as assigned by phase or therapeutic area. Duties and Responsibilities Act [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] within compliance and legal requirements as well as within company guidelines. Contribute positively to a strong culture of business integrity and ethics. Serve as liaison to project teams, CROs and others. Write abstracts and present data at scientific meetings, both internally and externally. Develop relationships with appropriate consultants. Represent development on project teams. Will [. .. ] and summarize safety data in ongoing studies for clinicians. Monitor, review and summarize safety and efficacy data in ongoing studies. Drafting of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports, CSRs and other FDA submissions. Preparation of clinical development plans. Development of protocols for clinical studies. Requirements Strong Analytical ability. Excellent written and oral communication skills. Ability to multi-task and work in a fast-paced environment. Prior Oncology Drug Development experience a plus. Minimum of relevant [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Abb Vie
Senior Clinical Research Associate
• Wiesbaden, Hesse
[. .. ] connecting stakeholders to the investigative sites and strengthening Abbvies positioning. Ability to motivate and align monitoring community through leadership and mentorship. Aligns, trains and motivates the site [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] staff and principal investigator on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership. Able to support, guide, and mentor junior personnel on Site Management activities. Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with [. .. ] therapeutic area indications with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials Superior knowledge on existing and emerging local regulatory and legal requirements, ICH/ GCP Guidelines and applicable policies. Demonstrate advanced communication skills and superior cross-functional collaboration skills among internal and external stakeholders. Demonstrate superior planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Superior ability to leverage technology, [. .. ]
Job am 06.03.2026 bei Neuvoo gefunden
IQVIA
Senior Clinical Operations Lead-Sponsor Dedicated (m/w/d)
• Berlin
[. .. ] documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents. Create Master ICF template and review/approve site changes (in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] consultation with legal, safety when warranted) . Update template for new risks and new amendments information. Participate in the feasibility and evaluation of investigative sites; working closing with the Clinical Trial Logistics group. Coordinate and monitor activities at investigational sites; review monitoring trip reports and support the US monitoring organization. Assist in the development and management of study timelines and priorities, including recruitment tools/ strategy and patient retentions plan. Plan and organize meetings with team support (eg. investigator/ coordinator meetings, DMC, SMC, safety call, etc. ) . Assist in the development of the IP and co-medication strategy (Quantities, labels, depots, tracking, etc. ) working closely with other departments. Participate in data review and discrepancy resolution. Participate in coordinating efforts with internal Pharmacovigilance, and safety group. Monitor study-[. .. ]
Job am 28.02.2026 bei Neuvoo gefunden
engineering people GmbH
Senior Clinical Contracting Specialist (m/w/d)
• Innenstadt, Hessen
Senior Clinical Contracting Specialist (m/w/d) Vollzeit Frankfurt am Main Entwicklung von Vertragsstrategien für komplexe, globale Studien Erstellung von Budget- und Vertragsvorlagen inklusive
Investigator-Grant-Schätzungen Sicherstellung der Compliance nach GCP/ ICH, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lokalen Gesetzen und Sponsorvorgaben Abstimmung mit Legal, Finance, RSU, Country Leads und Study Teams Analyse und Reporting von Contracting-KPIs in CTMS/ Tracking Tools Coaching von Kolleg:en und Durchführung von Trainings und Kundenpräsentationen Studium im Bereich Life Sciences, Recht, Gesundheitswissenschaften oder vergleichbare Qualifikation Erfahrung im Site-Contractingbei Sponsor oder CRO Erfahrung in a Vertrags- und Budgetverhandlungen mit [. .. ]
Job am 26.02.2026 bei Neuvoo gefunden
Norgine
National Engagement Lead (DACH) - Ultra Rare Diseases
• Wettenberg, Hesse
Führungs-/ Leitungspositionen
[. .. ] Maintain an in-depth understanding of technology, external regulation, and industry best practices through ongoing education, attending conferences, and reading specialist media. Compliance Governance In all activities comply [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with local legal, regulatory, and ethical requirements, and follow Norgines code of conduct and standard operating procedures to maintain compliance and integrity. Account performance metrics will be tracked and regular audits of field-activity conducted to verify separation of promotional and non-promotional duties. Completion of compliance training requirements specific to the execution [. .. ] medicine development objectives through facilitating Clinical Research (e. g. , non-interventional studies, registries, epidemiology projects, preclinical or translational research) . Liaise between potential researchers and the company on ISTs (Investigator Sponsored Trials) submission. Information and Business Advice Provide specialist advice on the interpretation and application of policies and procedures, resolving queries and issues and referring very complex or contentious issues to others. Requirements Bachelors Degree or Equivalent Level Life Sciences, Pharmacy, Medicine, or a related field. Masters degree or Ph D [. .. ]
Job am 23.02.2026 bei Neuvoo gefunden
GULP experts united
Medical Science Liaison Manager (m/f/d) Dermatology/ Neurotoxins
• Frankfurt, Hessen
[. .. ] and professional societies. -Present data at medical and scientific meetings, expert panels and continuing education events. -Collect and share field-related medical evidence to support internal strategies and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training. -Support investigator-initiated studies, clinical research and medical education initiatives. -Ensure compliance with all relevant legal, regulatory and corporate guidelines. Your profile-Degree in natural sciences (MD, Pharm D, Ph D or equivalent preferred) . -Previous experience in medical affairs, as an MSL or in relevant clinical settings (ideally in aesthetics, dermatology or neurotoxins) . -Excellent communication and presentation skills. -Willingness to travel within the assigned territory. -Self-[. .. ]
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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 32 offene Stellenanzeigen für Legal Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Legal Investigator Jobs?
Aktuell suchen 13 Unternehmen nach Bewerbern für Legal Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Legal Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Legal Investigator Stellenangebote:
- IQVIA (3 Jobs)
- PSI CRO (1 Job)
- Abb Vie (1 Job)
- engineering people GmbH (1 Job)
- Norgine (1 Job)
- GULP experts united (1 Job)
In welchen Bundesländern werden die meisten Legal Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Legal Investigator Jobs werden derzeit in Hessen (7 Jobs), Sachsen-Anhalt (4 Jobs) und Bayern (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Legal Investigator Jobs?
Legal Investigator Jobs gehören zum Berufsfeld Rechtswesen, Justiz und Verwaltung.
