Luminary Group

👥 1-10 Advertising Consulting Marketing Professional Services💼 Private Company

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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🔥 Biometrics Director

Posted 23 days ago

📍 United States

🔍 Pharmaceutical or biotechnology

🔧 Requirements

Master's or PhD in biostatistics, statistics, or a related field.
Minimum of 7 years of experience in biostatistics and data management in the pharmaceutical or biotechnology industry.
Prior experience in a leadership or management role.
Strong knowledge of statistical methodologies used in clinical trials, including sample size calculation and randomization.
Experience with statistical software such as SAS or R.
Experience with data management tools and clinical data standards.
Knowledge of regulatory guidelines and requirements related to biostatistics and data management.
Excellent communication and interpersonal skills.
Strong problem-solving and decision-making abilities.
High level of attention to detail and accuracy.
Publication record in peer-reviewed journals is desirable.

💡 Responsibilities

Lead and manage a team of biostatisticians and data managers, providing guidance and performance evaluations.
Develop and implement biostatistical and data management strategies for clinical trials across multiple therapeutic areas and phases.
Oversee the design of clinical trial protocols, including sample size calculations and statistical analysis plans.
Review and approve clinical trial documentation, including data management plans and statistical analysis plans.
Analyze clinical trial data using appropriate statistical methods, ensuring accuracy and reliability.
Ensure compliance with regulatory guidelines and industry standards.
Collaborate with cross-functional teams to integrate activities within the clinical development process.
Provide statistical expertise and support in regulatory interactions and submissions.
Participate in the development and review of clinical study reports and other regulatory documents.
Stay up-to-date with advancements in biostatistics and data management methodologies.
Contribute to process improvement projects.

Cross-functional collaborationData management

Posted 23 days ago

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🔥 Account Manager - Instruments/Diagnostics - Germany

Posted 23 days ago

📍 Germany

🔍 Chemistry/Diagnostics

🔧 Requirements

Prior experience as an Account Manager or Sales Manager within the Chemistry or Diagnostics industry.
Proven track record of managing and growing key accounts.
Strong knowledge of chemistry and diagnostic products and services.
Excellent communication and interpersonal skills, with the ability to build rapport with clients and internal stakeholders.
Ability to understand and articulate technical information to non-technical audiences.
Result-oriented mindset with a focus on customer satisfaction and business growth.
Strong organizational and time management skills, with the ability to prioritize tasks and meet deadlines.
Fluency in English and German is required, additional languages are a plus.
Bachelor's degree in a relevant field is preferred.

💡 Responsibilities

Develop and maintain strong relationships with key accounts, serving as the main point of contact and building trust and credibility.
Understand and anticipate customer needs and provide consultative solutions to drive customer satisfaction and retention.
Identify opportunities for upselling and cross-selling of products and services.
Work closely with cross-functional teams including R&D, Marketing, and Technical Support to ensure customer needs are met.
Monitor market trends and competitor activities to identify opportunities for growth and market expansion.
Provide regular reports and updates on account activities, sales forecasts, and market insights to senior management.
Participate in industry conferences, exhibitions, and events to build networks and promote our products and services.
Stay up-to-date with industry regulations and compliance requirements.

Account ManagementFluency in EnglishSales experienceTechnical support

Posted 23 days ago

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🔥 Account Executive - eClinical Solutions - UK & Nordics

Posted 23 days ago

📍 United Kingdom

🔍 EClinical Solutions

🔧 Requirements

Bachelor's degree in Business Administration, Healthcare Management, or a related field.
Minimum of [number] years of experience in sales or account management within the eClinical Solutions industry.
Proven track record of success in meeting or exceeding sales targets.
In-depth knowledge of eClinical Solutions and their applications in clinical trials and research.
Strong interpersonal and communication skills, with the ability to build and maintain relationships with diverse stakeholders.
Excellent presentation and negotiation skills, with the ability to effectively communicate the value of our solutions to clients.
Ability to work independently and as part of a team, with a high level of initiative and self-motivation.
Strong organizational and time management skills, with the ability to multitask and prioritize effectively.
Willingness to travel as needed to meet with clients and attend industry events.

💡 Responsibilities

Manage and grow a portfolio of client accounts within the eClinical Solutions space.
Develop and maintain strong relationships with key stakeholders, including C-level executives, project managers, and IT teams.
Understand client needs and challenges, and align our eClinical Solutions offerings to meet those needs.
Create and deliver compelling presentations and proposals to prospective clients, showcasing the value of our solutions.
Collaborate with cross-functional teams to ensure successful project implementation and customer satisfaction.
Monitor market trends and competitor activities to identify opportunities for business growth.
Meet and exceed sales targets, consistently driving revenue growth.
Provide regular reports on sales activities, pipeline development, and revenue projections.

RESTful APIsAccount ManagementNegotiation skillsClient relationship managementSales experienceCRM

Posted 23 days ago

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🔥 Biostatistician

Posted 23 days ago

📍 United Kingdom

🔍 Healthcare or pharmaceutical industry

🔧 Requirements

Master's or PhD in biostatistics, statistics, or a related field.
Minimum of 3 years of experience as a biostatistician in the healthcare or pharmaceutical industry.
Proficiency in statistical software such as SAS, R, or Python.
Strong knowledge of statistical methodologies and techniques, including linear regression, survival analysis, and Bayesian methods.
Experience with data analysis and interpretation in the context of clinical research or healthcare.
Familiarity with research study design and statistical analysis plans.
Excellent problem-solving and analytical skills.
Strong attention to detail and accuracy.
Ability to effectively communicate statistical concepts and findings to both technical and non-technical stakeholders.
Ability to work independently and collaboratively in a team setting.

💡 Responsibilities

Design and implement statistical methodologies for research studies and clinical trials.
Perform data analysis using appropriate statistical techniques and software.
Work closely with researchers and clinicians to develop study protocols and statistical analysis plans.
Ensure the quality, accuracy, and validity of statistical analyses and results.
Provide statistical input in the interpretation and communication of study findings.
Contribute to the development and review of research proposals, manuscripts, and presentations.
Stay up-to-date with the latest advancements in biostatistical methods and techniques.
Collaborate with cross-functional teams to support the integration of statistical analyses within the research process.
Contribute to the development and maintenance of statistical software tools and databases.
Adhere to regulatory guidelines and industry standards in relation to biostatistics.

PythonData Analysis

Posted 23 days ago

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🔥 Pharmacovigilence Manager - Poland (Remote)

Posted 3 months ago

📍 Poland

🔍 Life Sciences, pharma, biotech, and MedTech industries

🔧 Requirements

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.

💡 Responsibilities

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 ManagementCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationMultitaskingTeamworkTraining

Posted 3 months ago

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🔥 QPPV Manager Poland (Remote)

Posted 3 months ago

📍 Poland

🔍 Life Sciences

🔧 Requirements

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.

💡 Responsibilities

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 CoordinationCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationMultitaskingDocumentationTeamwork

Posted 3 months ago

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🔥 Local Person for Pharmacovigilance (LPPV) - Poland

Posted 3 months ago

📍 Poland

🔍 Life Sciences

🔧 Requirements

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.

💡 Responsibilities

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 3 months ago

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🔥 Managment Consultant - Regulatory/PV/Digital Consulting

Posted 3 months ago

📍 Germany, Switzerland, Austria, Belgium, Netherlands

🔍 Life sciences

🔧 Requirements

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.

💡 Responsibilities

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 LeadershipGoCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringNegotiationAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 3 months ago

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🔥 Senior Consultant - Regulatory/PV/Digital Consulting

Posted 3 months ago

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life Sciences

🔧 Requirements

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.

💡 Responsibilities

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 LeadershipCommunication SkillsAnalytical SkillsCollaborationProblem SolvingMentoringAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 3 months ago

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🔥 Prinicpal Consultant - Regulatory/PV/Digital Consulting

Posted 3 months ago

📍 Germany, Switzerland, Austria, United States, Denmark

🔍 Life sciences

🔧 Requirements

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.

💡 Responsibilities

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 3 months ago

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