Luminary Group

Luminary Group is an international executive search and business consultancy based in London, specializing in the Life Sciences and Pharmaceutical sectors. They offer expertise across various roles and disciplines, focusing on sourcing talent from C-Suite to Managerial levels and partnering with diverse clients, including innovative Start-Ups and established corporations.

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Jobs at this company:

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🔥 Pharmacovigilence Manager - Poland (Remote)

Posted 2024-11-22

📍 Poland

🔍 Life Sciences, pharma, biotech, and MedTech industries

University degree in Medicine, Pharmacy, or Life Science.
Several years’ experience in pharmacovigilance.
Knowledge of global and local pharmacovigilance guidelines and SOPs.
Ability to organize operational procedures and manage multiple tasks.
Polish language proficiency is a must; very good command of English.

Act as primary contact for PV for Competent Authority in the Territory, including 24/7 availability if legally required.
Interface between the EU-QPPV / Global PV team and local regulatory authority.
Set up and manage the local pharmacovigilance system.
Conduct local literature search, ICSR management, and signal detection.
Maintain local PSMF and organize data collection.
Participate in audits and provide monthly PV reports.

LeadershipProject ManagementData AnalysisProject CoordinationCross-functional Team LeadershipOperations ManagementData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationMultitasking

Posted 2024-11-22

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🔥 QPPV Manager Poland (Remote)

Posted 2024-11-22

📍 Poland

🔍 Life Sciences

University degree in Medicine, Pharmacy, or Life Science.
Several years of experience and profound knowledge in pharmacovigilance.
Expertise in global and local legislative guidelines related to pharmacovigilance.
Detailed knowledge of relevant SOPs (global and local).
Participation in relevant training courses.
Experience in operational tasks of the pharmacovigilance department.
Ability to organize procedures and manage multiple tasks.
Strong problem-solving and analytical skills.
Ability to work autonomously and in a team.
Fluent in Polish and very good English.

Act as primary contact for PV for Competent Authority in the Territory.
Interface between the EU-QPPV / Global PV team and local regulatory authority.
Set up and manage the local pharmacovigilance system.
Conduct local literature searches and manage local ICSR.
Perform PV intelligence screening and maintain local PSMF.
Oversee local data collection and adaptation/submission of PSUR/RMP.
Conduct local signal detection and implement risk minimization measures.
Review materials regarding local post-authorization safety.
Provide first-level medical information and PQC support.
Participate in PV audits/inspections and provide monthly PV reports.
Ensure PV training for affiliate employees and third parties.

Project ManagementData AnalysisProject CoordinationData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationMultitaskingDocumentation

Posted 2024-11-22

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🔥 Local Person for Pharmacovigilance (LPPV) - Poland

Posted 2024-11-21

📍 Poland

🔍 Life Sciences

University degree in Medicine, Pharmacy or Life Science.
Several years’ experience and profound knowledge in pharmacovigilance.
Expertise in relevant global and local legislative guidelines.
Detailed knowledge of related SOPs (global and local).
Experience in operative tasks performed by pharmacovigilance department members.
Ability to manage multiple tasks and adapt to challenging situations.
Strong analytical and problem-solving skills.
Ability to work autonomously and in a team.
Fluency in Polish is mandatory; very good command of English.

Act as primary contact for PV for Competent Authority in the Territory, including 24/7 availability if legally required.
Interface between the EU-QPPV / Global PV team at client and the local regulatory authority.
Set up and manage the local pharmacovigilance system.
Conduct Local Literature Searches and Local ICSR Management.
Carry out PV Intelligence Screening and maintain Local PSMF.
Organize local data collection and manage Local PVA.
Adapt and submit PSUR / RMP locally and perform local signal detection.
Implement additional Risk Minimization Measures and review post-authorization safety materials.
Provide first-level Medical Information and PQC Support.
Participate in PV-relevant audits and inspections.
Attend regular meetings and provide monthly PV reports.
Ensure PV training of affiliate employees, service providers, and Third Parties.

Posted 2024-11-21

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🔥 Managment Consultant - Regulatory/PV/Digital Consulting

Posted 2024-11-09

📍 Germany, Switzerland, Austria, Belgium, Netherlands

🔍 Life sciences

Bachelor's degree in a relevant field (Life Sciences, Regulatory Affairs, or related discipline); advanced degree (MS, PhD, or MBA) preferred.
A minimum of 10 years of experience in regulatory affairs, pharmacovigilance, and/or digital consulting within the life sciences industry.
Proven track record of successful project management and client relationship management.
In-depth knowledge of regulatory requirements in pharmacovigilance and digital solutions.
Exceptional leadership and interpersonal skills for engaging senior stakeholders.
Strong analytical and critical thinking skills for developing innovative solutions.
Excellent communication and presentation skills for technical information.
Demonstrated ability to work collaboratively in a fast-paced environment.
Willingness to travel for client engagements and industry events.

Develop and execute strategic consulting offerings in Regulatory Affairs, Pharmacovigilance, and Digital Transformation.
Build and maintain strong relationships with clients to understand their needs and regulatory obligations.
Lead high-impact projects, providing expert advice on regulatory submissions and compliance strategies.
Oversee integration of digital tools into consulting practices to improve client outcomes.
Collaborate with internal teams to create innovative solutions addressing client challenges.
Conduct market research and analyze trends in the life sciences sector.
Mentor and develop junior staff in professional development and technical expertise.
Represent Luminary Group at industry events to promote consulting capabilities.

LeadershipProject ManagementData AnalysisCross-functional Team LeadershipData analysisGoCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringNegotiationAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-09

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🔥 Consultant - Regulatory/PV/Digital Consulting

Posted 2024-11-09

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life Sciences

Bachelor's degree in Life Sciences, Regulatory Affairs, or a related discipline; advanced degree preferred.
A minimum of 10 years of experience in regulatory affairs, pharmacovigilance, and/or digital consulting.
Proven track record in project management and client relationship management.
In-depth knowledge of regulatory requirements and best practices in pharmacovigilance and digital solutions.
Exceptional leadership and interpersonal skills.
Strong analytical and critical thinking skills.
Excellent communication and presentation skills.
Demonstrated ability to work collaboratively in a fast-paced environment.
Willingness to travel as needed.

Develop and execute strategic consulting offerings in Regulatory Affairs, Pharmacovigilance, and Digital Transformation.
Build and maintain strong relationships with clients, ensuring deep understanding of their needs and regulatory obligations.
Lead high-impact projects providing expert advice on regulatory submissions and compliance strategies.
Oversee the integration of digital tools into consulting practices.
Collaborate with internal teams to create innovative solutions for client challenges.
Conduct market research to identify emerging trends and regulatory changes.
Mentor junior staff on professional development and technical expertise.
Represent the firm at industry conferences and workshops.

LeadershipProject ManagementData AnalysisCross-functional Team LeadershipData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communicationCompliance

Posted 2024-11-09

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🔥 Senior Consultant - Regulatory/PV/Digital Consulting

Posted 2024-11-09

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life Sciences

Bachelor's degree in a relevant field (Life Sciences, Regulatory Affairs, or related discipline); advanced degree (MS, PhD, or MBA) preferred.
A minimum of 10 years of experience in regulatory affairs, pharmacovigilance, and/or digital consulting within the life sciences industry.
Proven track record of project management and client relationship management in a consulting environment.
In-depth knowledge of regulatory requirements and best practices in pharmacovigilance and digital solutions.
Exceptional leadership and interpersonal skills to engage and influence stakeholders.
Strong analytical and critical thinking skills.
Excellent communication and presentation skills.
Demonstrated ability to work collaboratively in a fast-paced environment.

Develop and execute strategic consulting offerings in Regulatory Affairs, Pharmacovigilance, and Digital Transformation.
Build and maintain strong relationships with clients to understand their needs and regulatory obligations.
Lead high-impact projects providing expert advice on regulatory submissions and compliance strategies.
Oversee integration of digital tools into consulting practices.
Collaborate with internal teams to create innovative solutions for client challenges.
Conduct market research to identify trends and opportunities in the life sciences sector.
Mentor and develop junior staff.
Represent Luminary Group at industry events.

LeadershipProject ManagementData AnalysisPeople ManagementCross-functional Team LeadershipData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-09

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🔥 Prinicpal Consultant - Regulatory/PV/Digital Consulting

Posted 2024-11-09

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life sciences

Bachelor's degree in a relevant field (Life Sciences, Regulatory Affairs, or related discipline); advanced degree (MS, PhD, or MBA) preferred.
A minimum of 10 years of experience in regulatory affairs, pharmacovigilance, and/or digital consulting within the life sciences industry.
Proven track record of successful project management and client relationship management.
In-depth knowledge of regulatory requirements and best practices in pharmacovigilance and digital solutions.
Exceptional leadership and interpersonal skills to engage and influence senior stakeholders.
Strong analytical and critical thinking skills for developing innovative solutions.
Excellent communication and presentation skills for articulating technical information.

Develop and execute strategic consulting offerings in Regulatory Affairs, Pharmacovigilance, and Digital Transformation.
Build and maintain strong relationships with clients, understanding their needs and regulatory obligations.
Lead high-impact projects and provide expert guidance on regulatory submissions and compliance strategies.
Oversee the integration of digital tools into consulting practices.
Collaborate with internal teams to create solutions addressing client challenges.
Conduct market research to identify trends and new opportunities.
Mentor junior staff and provide industry guidance.
Represent the company at conferences, workshops, and seminars.

LeadershipProject ManagementProject CoordinationGoCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringNegotiationAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-09

Apply

🔥 Managment Consultant - Regulatory/PV/Digital Consulting

Posted 2024-11-09

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life sciences

Bachelor's degree in a relevant field (Life Sciences, Regulatory Affairs, or related discipline); advanced degree preferred (MS, PhD, or MBA).
Minimum of 10 years of experience in regulatory affairs, pharmacovigilance, and/or digital consulting within the life sciences industry.
Proven track record of successful project management and client relationship management.
In-depth knowledge of regulatory requirements and best practices in pharmacovigilance and digital solutions.
Exceptional leadership and interpersonal skills to engage and influence senior stakeholders.
Strong analytical and critical thinking skills to develop innovative solutions for clients.
Excellent communication and presentation skills for articulating technical information.
Demonstrated ability to work collaboratively in a fast-paced environment.
Willingness to travel as needed.

Develop and execute strategic consulting offerings in Regulatory Affairs, Pharmacovigilance, and Digital Transformation.
Build and maintain strong relationships with clients, ensuring a deep understanding of their needs.
Lead high-impact projects, providing guidance on regulatory submissions and compliance strategies.
Oversee integration of digital tools to enhance efficiency for clients.
Collaborate with internal teams to create innovative solutions for client challenges.
Conduct market research to identify emerging trends in the life sciences sector.
Mentor junior staff on professional development and technical expertise.
Represent Luminary Group at industry events to promote consulting capabilities.

LeadershipProject ManagementCross-functional Team LeadershipStrategyGoCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringNegotiationAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-09

Apply

🔥 Principal Partner - Regulatory/PV/Digital Consulting

Posted 2024-11-09

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life sciences

Bachelor's degree in Life Sciences, Regulatory Affairs, or a related discipline; advanced degree (MS, PhD, or MBA) preferred.
Minimum of 10 years of experience in regulatory affairs, pharmacovigilance, and/or digital consulting within the life sciences industry.
Proven track record in project management and client relationship management.
In-depth knowledge of regulatory requirements and best practices in pharmacovigilance and digital solutions.
Exceptional leadership and interpersonal skills to effectively engage senior stakeholders.
Strong analytical and critical thinking skills for developing innovative client solutions.
Excellent communication and presentation skills for articulating technical information to non-technical audiences.
Ability to work collaboratively in a dynamic environment.
Willingness to travel for client engagements and industry events.

Develop and execute strategic consulting offerings in Regulatory Affairs, Pharmacovigilance, and Digital Transformation.
Build and maintain strong client relationships, understanding their needs and regulatory obligations.
Lead high-impact projects providing expert guidance on regulatory submissions and compliance strategies.
Oversee integration of digital tools into consulting practices to enhance client outcomes.
Collaborate with internal teams to create innovative solutions for client challenges.
Conduct market research to identify trends and new opportunities in the life sciences sector.
Mentor junior staff, providing guidance on their professional development.
Represent the company at industry conferences to promote consulting capabilities.

Posted 2024-11-09

Apply

🔥 Senior Business Development Director - Regulatory/PV Consulting

Posted 2024-11-09

📍 United States, Portugal, Spain, United Kingdom, Germany

🔍 Life science industry

Bachelor's degree in Business Administration, Life Sciences, or related field; advanced degree (MBA, PhD) preferred.
Minimum of 5 years of experience in business development, sales, or consulting within the life science industry.
Proven track record of success in driving revenue growth and meeting sales targets.
Strong network of contacts within the pharmaceutical, biotechnology, and medical device industries.
Excellent communication and presentation skills, with the ability to effectively engage and influence clients.
Ability to understand and articulate complex scientific and business concepts to both technical and non-technical audiences.
Strong analytical and problem-solving skills, with the ability to identify client needs and propose innovative solutions.
Entrepreneurial mindset with the ability to thrive in a fast-paced and dynamic environment.
Willingness to travel as needed to meet with clients and attend industry events.

Develop and implement strategic business development plans to generate new leads and opportunities within the life science industry.
Identify and target potential clients by conducting market research and analysis.
Build and maintain strong relationships with key decision-makers in pharmaceutical, biotechnology, and medical device companies.
Collaborate with cross-functional teams to develop customized solutions and proposals for clients.
Manage the entire sales process, from lead generation and qualification to contract negotiation and closing deals.
Stay updated on industry trends and market developments to identify new growth opportunities.
Represent the company in industry conferences, trade shows, and networking events.
Provide regular reports on sales activities, pipeline development, and revenue projections.

LeadershipProject ManagementBusiness DevelopmentData AnalysisPeople ManagementProject CoordinationStrategyBusiness developmentData analysisGoCommunication SkillsAnalytical SkillsCollaborationProblem SolvingNegotiationAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-09

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Luminary Group

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