Luminary Group

πŸ‘₯ 1-10AdvertisingConsultingMarketingProfessional ServicesπŸ’Ό Private Company
Website LinkedIn Email Facebook Twitter

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.

Related companies:

🏒 Cartwheel
πŸ‘₯ 1-10πŸ’° $5,600,000 Seed 10 months ago
Website LinkedIn

Jobs at this company:

Apply

πŸ“ Italy, Albania, Romania

πŸ” Pharmacovigilance

  • Fluency in Italian and English, both written and spoken.
  • Minimum of 2 years of experience in Pharmacovigilance or a related field.
  • Strong knowledge of Pharmacovigilance practices and regulations.
  • Experience with case processing activities, including data entry, coding, and narrative writing.
  • Proficiency in using Pharmacovigilance databases and safety reporting systems.
  • Ability to work independently and prioritize tasks effectively.
  • Excellent attention to detail and accuracy in data entry and documentation.
  • Strong analytical and problem-solving skills.
  • Good interpersonal and communication skills, with the ability to effectively collaborate with cross-functional teams.
  • Experience with MedDRA coding and EudraVigilance is desirable.
  • Knowledge of other European languages is a plus.
  • Flexibility to work in different time zones, if required.
  • Review and evaluate adverse event reports and other safety-related information for our client's products.
  • Perform case processing activities, including data entry, coding, narrative writing, and quality checks.
  • Conduct signal detection activities and contribute to the preparation of signal evaluation reports.
  • Collaborate with cross-functional teams to ensure timely and accurate reporting of adverse events to regulatory authorities.
  • Participate in the development and implementation of Pharmacovigilance processes and procedures.
  • Assist in the training and mentoring of junior team members.
  • Maintain knowledge of current regulatory requirements and guidelines related to Pharmacovigilance.
  • Ensure compliance with company policies and standard operating procedures.
  • Contribute to the continuous improvement of Pharmacovigilance activities and systems.

Analytical SkillsComplianceExcellent communication skillsProblem-solving skillsFluency in EnglishData entryData management

Posted 13 days ago
Apply
Apply
πŸ”₯ Biometrics Manager
Posted 2 months ago

πŸ“ United States

πŸ” Pharmaceutical or biotechnology industry

  • 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, randomization, and statistical analysis.
  • 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, with the ability to effectively collaborate with cross-functional teams and external stakeholders.
  • Strong problem-solving and decision-making abilities.
  • A high level of attention to detail and accuracy.
  • Publication record in peer-reviewed journals is desirable.
  • Lead and manage a team of biostatisticians and data managers, providing guidance, mentorship, 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, data validation plans, and statistical analysis plans.
  • Analyze clinical trial data using appropriate statistical methods, ensuring accuracy, consistency, and reliability of results.
  • Ensure compliance with regulatory guidelines and industry standards in relation to biostatistics and data management.
  • Collaborate with cross-functional teams to integrate biostatistical and data management 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, statistical summary reports, and other regulatory documents.
  • Stay up-to-date with the latest advancements in biostatistics and data management methodologies.
  • Contribute to departmental initiatives and process improvement projects.

LeadershipData management

Posted 2 months ago
Apply
Apply

πŸ“ United States

πŸ” Pharmaceutical or biotechnology

  • 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.
  • 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 2 months ago
Apply
Apply

πŸ“ Germany

πŸ” Chemistry/Diagnostics

  • 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.
  • 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 2 months ago
Apply
Apply

πŸ“ Germany

πŸ” Chemistry/Diagnostics

  • 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 to build rapport with clients and internal stakeholders.
  • Ability to articulate technical information to non-technical audiences.
  • Result-oriented mindset focusing on customer satisfaction and business growth.
  • Strong organizational and time management skills with the ability to prioritize tasks.
  • Fluency in English and German; additional languages are a plus.
  • Bachelor's degree in a relevant field preferred.
  • Develop and maintain strong relationships with key accounts, serving as the main point of contact.
  • Understand and anticipate customer needs and provide consultative solutions to drive satisfaction and retention.
  • Identify opportunities for upselling and cross-selling products and services.
  • Collaborate with R&D, Marketing, and Technical Support teams to meet customer needs.
  • Monitor market trends and competitor activities for growth opportunities.
  • Provide regular reports on account activities, sales forecasts, and market insights to senior management.
  • Participate in industry conferences and events to promote products and build networks.
  • Stay updated with industry regulations and compliance requirements.

Account ManagementFluency in EnglishRelationship managementSales experienceMarket ResearchTechnical support

Posted 2 months ago
Apply
Apply

πŸ“ United Kingdom

πŸ” EClinical Solutions

  • 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.
  • 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 2 months ago
Apply
Apply
πŸ”₯ Biostatistician
Posted 2 months ago

πŸ“ United Kingdom

πŸ” Healthcare or pharmaceutical industry

  • 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.
  • 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 2 months ago
Apply
Apply

πŸ“ Boston, Massachusetts, United States

πŸ” Pharmaceutical or biotechnology industry

  • 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, randomization, and statistical analysis.
  • 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.
  • A high level of attention to detail and accuracy.
  • Publication record in peer-reviewed journals is desirable.
  • Lead and manage a team of biostatisticians and data managers, providing guidance, mentorship, 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, data validation plans, and statistical analysis plans.
  • Analyze clinical trial data using appropriate statistical methods, ensuring accuracy, consistency, and reliability of results.
  • Ensure compliance with regulatory guidelines and industry standards in relation to biostatistics and data management.
  • Collaborate with cross-functional teams to integrate biostatistical and data management 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, statistical summary reports, and other regulatory documents.
  • Stay up-to-date with the latest advancements in biostatistics and data management methodologies.
  • Contribute to departmental initiatives and process improvement projects.

LeadershipData management

Posted 2 months ago
Apply
Apply

πŸ“ Poland

πŸ” 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 ManagementCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationMultitaskingTeamworkTraining

Posted 4 months ago
Apply
Apply

πŸ“ Poland

πŸ” 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 CoordinationCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationMultitaskingDocumentationTeamwork

Posted 4 months ago
Apply
Shown 10 out of 30