33 Jobs für Legal Investigator
Stellenangebote Legal Investigator Jobs
Job gestern bei Jooble gefunden
• München
[. .. ] 10-15 yrs of working experience (clinical practice +/-industry) post their residency/ fellowship. Its not necessary that they are licensed in US or specific country (pls check country [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] local legal requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal Additional Points: Clinical practice experience of minimum 4 yrs is mandatory. Normally the Study Physician position is higher or at [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Contracts Manager-Germany
• Homeoffice
Work-Life-Balance
[. .. ] region. We are searching for a professional who has already direct experience in both contract negotiation and managing clinical research budgets with sites. Your responsibilities would also [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] include reviewing the legal wording of the clinical site contracts and so any prior experience in legal or contract writing would be nice to have. What you will be doing: Serve as a contact negotiator for all study related contract activities to meet the business objectives Maintain active/ frequent communication with internal/ external partners and/or investigators and internal departments regarding research contracts throughout the contract lifecycle Assist in developing investigator baseline budgets Review and negotiate the terms and conditions for various types of incoming and outgoing contracts and budgets in accordance with internal policy and ICH-GCP regulations Prepare subsequent contract amendments, note to files and other contract activities, as needed Develop and maintain status trackers, prepare start-up and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
• München
[. .. ] 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 company s key [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
Associate Director, Medical Affairs Dermatology (Atopic Dermatitis) (m/f/d)
• München
Führungs-/ Leitungspositionen
[. .. ] for assigned products and therapeutic areas Ensures appropriate execution of medical content elements of the tactical plan for assigned product (s) and therapeutic area (s) Acts within [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance, regulatory and legal requirements as well as within company guidelines Demonstrates medical and scientific expertise to core business strategy and marketing/ business development plans, strongly contributes to the development of and updates to the strategic medical plans Ensuring that strategically aligned scientific communication points, elements from other internal guidance and resource documents, and [. .. ] leadership and actively contributes to market access dossiers Oversee the agenda development, content creation, and execution for educational symposia, internal meetings/ summits and advisory boards Supports advisory board meetings and investigator meetings. Provides support for content development and delivering clinical presentations at medical meetings Develops and delivers presentations to colleagues and management as needed, provides strong input to briefing documents, written communications, Frequently Asked Questions documents, backgrounders, newsletters, slide decks, and medical information letters etc. MD, Pharm D or Ph D in life [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice
[. .. ] a team of CTMs. A day in the Life: Leads the local study team consisting of within-country clinical operations team members, cross-functional experts (medical, regulatory, supply logistics, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] finance, legal, etc. ) , vendor staff, and external clinical site staff involved in study preparation and delivery providing both matrix leadership and project management of study activities within the country (ies) . Serves as the operational point-of-contact between the central study team and within-country (ies) study team. The [. .. ] required, advises support/ develops and negotiates on contract development with Sites/ CRO/ Vendors ensuring legal input where required and may participate in budget/ contract negotiations with study vendors or clinical investigator sites. As required, selects manages local vendors in accordance with local practices in alignment with overall resourcing strategy for the study; accountable for local vendor management including oversight, agreements, payments, communications issue management. Manages the development of key study documents, plans manuals according to local requirements (monitoring plan, local informed [. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
[. .. ] 10-15 yrs of working experience (clinical practice +/-industry) post their residency/ fellowship. Its not necessary that they are licensed in US or specific country (pls check country [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] local legal requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal Additional Points: Clinical practice experience of minimum 4 yrs is mandatory. Normally the Study Physician position is higher or at [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Incyte Corporation
• Homeoffice
[. .. ] (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 vor 3 Tagen bei Jooble gefunden
Incyte Corporation
Medical Science Liaison Dermatology (m/f/d) - Münster, Dortmund, Bielefeld
• Homeoffice
[. .. ] (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 15.01.2026 bei Jooble gefunden
• München
Führungs-/ Leitungspositionen
[. .. ] internal customers to seek assistance. Oversees negotiations of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language terms, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] financial attachments, and investigator grant budgets in collaboration with a global team of site contract budget negotiators. Advises study team and Sponsor stakeholders on industry trends, norms, and emergent developments surrounding site contract and budgetary negotiations. Provides consultation on potential risks and mitigation tactics for negotiation issues pertaining to overall study start-up needs. [. .. ] solutions. Establishes strong working relationships with customer and internal project teams. Escalates deviations to senior management and is equipped to resolve issues with Quality Assurance. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Identifies best practices, investigates root causes of fundamental issues and problems for projects and recommends solutions. Trains and mentors less experienced staff members on department Standard Operating Procedures (SOPs) , processes, tools and templates and ensures quality [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
AOP Health
Manager Product Quality Compliance (m/f/d)
• AT- 9 Wien
Homeoffice möglich
[. .. ] Your Day To Day Will Look Like Product Quality Incident Management Manage product-related incidents, including out-of-specification (OOS) results, bioburden and particle issues, deviations Act as quality function, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] investigator, and/or subject matter expert for assigned cases Ensure timely, compliant investigations, root cause analyses, and implementation of effective CAPAs Functionally guide and coach more junior colleagues in the team in incident handling, including investigation strategy, root cause analysis, documentation, and CAPA definition Complaint Handling Oversee and handle product quality [. .. ] public transport connections (U4-Heiligenstadt) Flexible working hours (flexitime/ time-out days) , bonus scheme, additional benefits and employee events Structured onboarding and support through a buddy system Due to legal requirements, we are obliged to disclose the collective agreement minimum salary, which is EUR 45, 080 gross per year, based on full-time employment. However, our actual remuneration packages are market-oriented and aligned with your qualifications and professional experience. Benefits Bonus Homeoffice Company car Employee mobile phone Flexible working [. .. ]
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 6 Std. bei Jobleads gefunden
• Zürich Zuerich
[. .. ] embedded in the groups cutting-edge research activities. Research Project Grant Coordination Take responsibility for coordinating externally funded research projects (e. g. SNSF, ERC) in close collaboration with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Principal Investigator (s) , including managing timelines, deliverables, and coordination processes across international research teams Support the strategic development, preparation, and submission of grant applications by coordinating inputs, timelines, and partner contributions from multiple institutions and countries; contribute to proposal development where appropriate Oversee scientific and financial reporting requirements for funded projects in coordination with ETH central administration and international project partners Support contract-related processes (e. g. research agreements, collaboration agreements) and act as a liaison with ETH grants, legal, and research offices, as well as external partner institutions Group External Research Coordination Coordinate research activities, milestones, and workflows across multiple projects and group members in a diverse, international research environment Serve as a central coordination point between the group and collaborating research teams at ETH Zurich and partner institutions [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Dermatology (m/f/d) - Münster, Dortmund, Bielefeld
[. .. ] 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 [. .. ]
Neu Job vor 6 Std. 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 [. .. ]
Neu Job vor 6 Std. 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 vor 3 Tagen bei Jobleads gefunden
Senior Research Coordinator/ Lab Manager
• Zürich Zuerich
[. .. ] the groups cutting-edge research activities. Job description Research Project Grant Coordination Take responsibility for coordinating externally funded research projects (e. g. SNSF, ERC) in close collaboration with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Principal Investigator (s) , including managing timelines, deliverables, and coordination processes across international research teams Support the strategic development, preparation, and submission of grant applications by coordinating inputs, timelines, and partner contributions from multiple institutions and countries; contribute to proposal development where appropriate Oversee scientific and financial reporting requirements for funded projects in coordination with ETH central administration and international project partners Support contract-related processes (e. g. research agreements, collaboration agreements) and act as a liaison with ETH grants, legal, and research offices, as well as external partner institutions Group External Research Coordination Coordinate research activities, milestones, and workflows across multiple projects and group members in a diverse, international research environment Serve as a central coordination point between the group and collaborating research teams at ETH Zurich and partner institutions [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Senior Director, Regulatory Compliance, Large Molecule (Switzerland)
• Zuchwil, Solothurn
Führungs-/ Leitungspositionen
Job title Senior Director, Regulatory Compliance, Large Molecule (Switzerland) Function
Legal Compliance Sub function Enterprise Compliance Category Senior Director, Enterprise Compliance (PL10) Location Zuchwil/ Switzerland Date posted Jan 12 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2026 Requisition number R-052854 Work pattern Fully Onsite Description At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases [. .. ] FDA, EMA or MHRA in the context of biologics manufacturing. Handson operational knowledge of cell banks, upstream cell culture, downstream purification, analytical labs and CMOs for biologics. Experience as an Investigator for the US FDA is also acceptable. Knowledge, Skills, and Abilities Expertise in biologics modalities, viral clearance/ inactivation strategies, potency/ assay strategy, stability and comparability assessments. Demonstrated success implementing inspection readiness, audit programs and vendor oversight for large molecule products. Proven experience collaborating with, or working for, regulatory agencies or [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
[. .. ] triage and investigation of complex integrity matters, provide evidencebased advice to executive leaders, and strengthen organisational capability through education, guidance and proactive fraud and corruption prevention. If [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] youre an experienced investigator with sound judgement, maturity and the ability to navigate sensitive issues with discretion, this is your opportunity to make a meaningful impact across Council. Responsibilities Lead endtoend integrity matters triage, assess and investigate complaints, public interest disclosures and misconduct matters in line with legislation and Council policy Deliver highquality investigations [. .. ] People with criminal records are not automatically barred from applying for this position; each application will be considered on its merits. To be eligible for employment, applicants must have the legal right to work in Australia. Why this role stands out Enjoy flexible work options which help you balance your career and lifestyle. Be part of a small team where your work creates real impact. Work on the Redlands Coast, surrounded by inspiring natural beauty. More reasons to love working with [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Manager Product Quality Compliance (m/f/d)
• Wien
Homeoffice möglich
[. .. ] Your Day To Day Will Look Like Product Quality Incident Management Manage product-related incidents, including out-of-specification (OOS) results, bioburden and particle issues, deviations Act as quality function, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] investigator, and/or subject matter expert for assigned cases Ensure timely, compliant investigations, root cause analyses, and implementation of effective CAPAs Functionally guide and coach more junior colleagues in the team in incident handling, including investigation strategy, root cause analysis, documentation, and CAPA definition Complaint Handling Oversee and handle product quality [. .. ] public transport connections (U4-Heiligenstadt) Flexible working hours (flexitime/ time-out days) , bonus scheme, additional benefits and employee events Structured onboarding and support through a buddy system Due to legal requirements, we are obliged to disclose the collective agreement minimum salary, which is EUR 45, 080 gross per year, based on full-time employment. However, our actual remuneration packages are market-oriented and aligned with your qualifications and professional experience. Benefits Bonus Homeoffice Company car Employee mobile phone Flexible working [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Head of Medical Affairs, Germany
• München, Bayern
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] a strategic medical partner to the German General Manager and other cross functional partners. Ensure scientific and ethical rigour in all affiliate activities, collaborating effectively with Marketing, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Market Access, Commercialisation, Legal, QA, Regulatory, and other Research Development and Enabling functions. Establish and track clear medical performance metrics (KPIs) and ensure readiness for quarterly business reviews (QBRs) to drive accountability and continuous improvement. Medical Strategy and Leadership Develop and oversee German Medical Affairs strategy in alignment with European and global medical affairs [. .. ] ensure a consistent regional global scientific narrative. Scientific Communication Evidence Generation Provide German medical/ scientific perspective with targeted insight compilation, analysis to inform clinical development commercialisation planning Oversee pan-portfolio investigator interactions to enhance medical/ scientific exchange optimise study execution in Germany Supervise dissemination discussion of Genmabs scientific/ clinical data with investigators and other appropriate HCPs Develop and execute national conference plans, ensuring active participation in relevant professional society events Enable externally sponsored German evidence generation initiatives Partner with CORE/ Market [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] internal customers to seek assistance. Oversees negotiations of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language terms, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] financial attachments, and investigator grant budgets in collaboration with a global team of site contract budget negotiators. Provides oversight of contact budget negotiations status and manages escalation of out-of-parameter queries on budgetary and contractual requests to sponsor decision-makers in all regions of study conduct. Provides consultation during escalation of out-of-[. .. ] Quality Assurance. Creates and maintains document status reports, and updates department tools/ systems and team members on a regular basis; ensures appropriate documentation is maintained. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites. Identifies best practices, investigates root causes [. .. ]
Job am 18.01.2026 bei Jobleads gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] internal customers to seek assistance. Oversees negotiations of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language terms, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] financial attachments, and investigator grant budgets in collaboration with a global team of site contract budget negotiators. Provides oversight of contract budget negotiations status and manages escalation of out-of-parameter queries on budgetary and contractual requests to sponsor decision-makers in all regions of study conduct. Provides consultation during escalation of out-of-[. .. ] Quality Assurance. Creates and maintains document status reports, and updates department tools/ systems and team members on a regular basis; ensures appropriate documentation is maintained. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites. Identifies best practices, investigates root causes [. .. ]
Job am 18.01.2026 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 Facilitate collaborative exchange between BMS and thought leaders in [. .. ] . 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 [. .. ]
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 [. .. ]
1 von 2Weiter » Weitere Suchergebnisse laden »
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 33 offene Stellenanzeigen für Legal Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Legal Investigator Jobs?
Aktuell suchen 10 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:
- Incyte Corporation (4 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- ICON (1 Job)
- AOP Health (1 Job)
- Erbe (1 Job)
- Erbe Elektromedizin GmbH (1 Job)
In welchen Bundesländern werden die meisten Legal Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Legal Investigator Jobs werden derzeit in Hessen (5 Jobs), Bayern (4 Jobs) und Sachsen-Anhalt (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Legal Investigator Jobs?
Legal Investigator Jobs gehören zum Berufsfeld Rechtswesen, Justiz und Verwaltung.
