The Associate Director (AD) Client Services is responsible for the client relationships and operational delivery for a portfolio of CFS projects.$112.3k-151.7k yearly11d ago
Associate Director, Screening and Bioanalytical
Responsible for leading a team of ADME professionals and people managers who exercise latitude and independence in assignments. Partners with executive and global leadership to establish strategy and ensure implementation to drive achievement of annual objectives and supporting long term success.
**RESPONSIBILITIES:**
• Responsible for policy and strategy implementation for short term result.
• Serves as technical lead and subject matter expert.
• Serves as a key point of contact for clients for RFP's, complex problem resolution, and to support business development efforts.
• Oversight of the team's client interactions to ensure effectiveness and mentors team to develop client facing competency.
• Leads complex technical projects for the organization, often on a global scale.
• Responsible for hiring, onboarding, and performance management of team.
• Responsible for ensuring effective resourcing to meet client and budgetary expectations.
• Sets goals and objectives for team members for achievement of operational and strategic results with short to mid-term timeframe.
• Drives innovation and develops new products, processes, standards or operational plans in support of the job function strategy.
• Monitor utilization patterns of services and advise on developing trends in industry needs.
• Contributes to the development and achievement of the department's operating budget.
• Makes recommendations to senior leadership for budget oversight.
• Responsible for achievement of revenue targets.
• Responsible for mentoring and development of team members.
• Responsible for ensuring alignment to scientific quality standards.
• Fosters a unified culture and facilitates collaboration, cooperation, sharing of information and teamwork.
• Leads initiatives to improve employee engagement to positively impact operational results, customer satisfaction and employee retention.
• Manages staff in accordance with organization's policies and applicable regulations.
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE:**
• Bachelor's Degree in chemistry, biology, or related field required.
• Bachelor's Degree plus 10 years of related experience in method development or specific methodology area or Master's Degree plus 7 years of related experience or PhD plus 5 years of related experience or equivalent combination of education, training and experience in a bioanalytical laboratory environment.
• 5 years of line management experience.
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:**
• Requires broad management knowledge to lead teams, as well as the ability to influences others outside of own job area regarding policies, procedures, and goals.
• Requires comprehensive knowledge of method development, drug development and ADME scientific principles, theories, concepts, and state of the art instrumentation.
• Strong knowledge of the drug development industry and demonstrated ability to apply that knowledge to the improvement of their business unit.
• Effective organizational and interpersonal skills.
• Skilled in extracting relevant data to measure performance indicators to proactively plan for efficiency, growth, and scalability.
• Ability to lead and motivate high-performing teams.
• Ability to manage multiple projects and ensure that they are performed in a quality manner.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Effective communication and presentation skills to influence at various levels of the business, including senior leadership.
Q² Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. https://www.q2labsolutions.com/careers
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/q2-solutions-eoe
As the COVID-19 virus continues to evolve, Q² Solutions' ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status
IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled$97k-122k yearly est.60d+ ago
Associate Director, Global Project Leadership
IQVIA's Associate Directors within Global Project Leadership specialise in one of our seven global therapeutic areas to manage and support the operational elements and execution of studies and/or programs. In collaboration with study/program teams, you will leverage deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our customers. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.$109k-137k yearly est.60d+ ago
Associate Director, Statistics (FSP)
IQVIA is seeking an Associate Director of Statistics with excellent experience in operational tasks to support the Hematology group for a top FSP client.$109k-137k yearly est.60d+ ago
Associate Director, Epidemiology, Real World Evidence
The Associate Director (AD), Epidemiology, will work in IQVIA's Center for Advanced Evidence Generation, using epidemiological knowledge to drive innovation and research. This individual will lead strategic initiatives across IQVIA, write manuscripts, contribute to proposals, and protocol design. + Serves as key team member in the Center for Advanced Evidence Generation, developing strategy and contributing to leadership initiatives across IQVIA. + Represents IQVIA externally through conference presentations. + Works collaboratively on inter-disciplinary teams, internal and external to IQVIA IQVIA is a leading glo$109k-137k yearly est.60d+ ago
Associate Director, Epidemiology, Real World Evidence
The Associate Director (AD), Epidemiology, will work in IQVIA's Center for Advanced Evidence Generation, using epidemiological knowledge to drive innovation and research. This individual will lead strategic initiatives across IQVIA, write manuscripts, contribute to proposals, and protocol design. + Serves as key team member in the Center for Advanced Evidence Generation, developing strategy and contributing to leadership initiatives across IQVIA. + Represents IQVIA externally through conference presentations. + Works collaboratively on inter-disciplinary teams, internal and external to IQVIA IQVIA is a leading glo$113k-145k yearly est.60d+ ago
Associate Director of Architecture
**Overview** **IQVIA ** is the world's leading company providing information, technology, and services for virtually every type of stakeholder in healthcare. Every day, IQVIA innovates on a large scale. IQVIA stores and computes more than 20 petabytes of complex healthcare data on diseases, treatments, costs and outcomes to enable our clients to run their operations more efficiently. IQVIA employs over 50,000 professionals in over 100 countries to drive results for over 5,000 healthcare clients globally. IQVIA is a publicly listed company (NYSE - Q) with estimated revenue close to $7B and a market cap of over $18B. **IQVIA Commercial Solutions** provides tools to the Life Sciences industry in countries around the world. **Job Summary:** The Associate Director will assist with the conceptualization, development and deployment of an enterprise architecture which supports current and future IQVIA systems, products and platforms and that satisfies business product strategy.$109k-137k yearly est.60d+ ago
Associate Director, Immunoassay Services (Sign on Bonus Offered)
**RESPONSIBILITIES**
+ Establish strategies and priorities of the Immunoassay Services group.
+ Manage budget formulation for the Immunoassay Services group.
+ Lead the operation of the Immunoassay Services group through the managerial structure and individual scientific staff.
+ Ensures business unit operates effectively and efficiently.
+ Ensures that the Immunoassay Services group has sufficient resources to meet its goals.
+ Provide scientific leadership for Method Development, Validation and Sample Analysis.
+ Review and approve reports and other regulatory documentation as priorities dictate.
+ Act as scientific resource for Bioanalysis functions at Q2 Solutions.
+ Present and represent the scope and capabilities of Immunoassay Services group to clients and auditors
+ Support human resource policy and timely adherence to performance management guidelines for all assigned staff.
+ Upholding all safety standards, discipline guidelines and regulatory compliance requirements
+ Assist sales with business development opportunities.
+ Maintain a detailed awareness of industry guidance and standards for assay development & validation and performance and maintain current knowledge of advancing technologies and propose their applications to ongoing projects.
+ Participate in scientific meetings and produce original peer-reviewed publications. Perform research and development activities to support new assay development and assess new technologies or formats to maintain industry leading capabilities.
+ Oversee daily management of intra- and inter-organizational relationships to ensure timely completion of projects in accordance with customer specification.
+ Prepare and make external presentations of Immunoassay capabilities to clients and prospective clients.
+ Apply analytical skills to assist in the development and implementation of profit-generating assays.
+ Comply with all applicable regulatory standards, including Good Clinical and Good Laboratory Practices.
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Advanced understanding of ligand binding immunoassays and analytical instrumentation for
+ chromogenic ELISA, chemiluminescence, fluorescence and electrochemiluminescence assays.
+ Experience in neutralizing antibody (NAb) assay development and execution preferred. This includes
+ expertise in developing, maintaining, and banking cell lines and experience developing and validating cell-based assays.
+ Experience with BSL-3 preferred.
+ Experience in genomic method such as PCR utilized for the quantitation of cell and gene therapy vectors.
+ Experience in automating workflows and incorporation of laboratory automation and liquid handling systems.
+ Understanding of all routine laboratory procedures.
+ Demonstrated experience in writing technical reports and procedures.
+ Understanding of development/validation of methodology.
+ Understanding of wet laboratory workflows and an eye for efficiency and innovation in delivery.
+ Ability to interact with clients, and work to objectives/timelines.
+ Excellent attention to detail and communication skills.
+ Ability to maintain clear and efficient documentation.
+ Ability to provide verbally communicated or draft procedures.
+ Demonstrated ability to train staff of various skill levels.
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ PhD with 5 years of regulated immunoassay experience preferred, master's degree with 5-7 years of CRO experience or bachelor's degree in Biology/Chemistry/Biochemistry or a related field with 10 years of experience or equivalent combination of education, training, and experience in GLP laboratory environment.
+ Minimum of 5 years supervising a team.
Q² Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. https://www.q2labsolutions.com/careers
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/q2-solutions-eoe
As the COVID-19 virus continues to evolve, Q² Solutions' ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status
IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled$109k-137k yearly est.60d+ ago
Associate Director, Strategic Planning and Feasibility Lead
**Main responsibilities:**
+ Accountable and responsible for developing trial level feasibility and strategic allocation plans, aligned with global indication/program feasibility and allocation strategy, within assigned Development Unit(s), and according to portfolio prioritization.
+ Leads multidisciplinary Trial Feasibility Team with GCTs and/or CTTs, Regions and COs to develop validate and refine allocation strategy, including timelines and scenarios and risk mitigation plans. Identifies and resolves events in the indication landscape that represent operational risks for the execution of clinical trials within the given indication/program. Leads integration of regional and local indication strategies within global execution plans.
+ Key contributor to feasibility strategy within assigned trial(s); provide global feasibility input into protocol development and/or trial design, based on health insights and feasibility assessment from Global Health Insight Directors, Regions and/or Countries. Ensures feedback from feasibility assessment is addressed.
+ Leads analyses of clinical intelligence data describing the indication landscape, including scientific and epidemiology data, competitive intelligence, treatment paradigms and potential site partners globally, from external and internal research data sources, based on the clinical intelligence package received from Health Insights Manager.
+ Develops risk management strategies for clinical trial(s) highlighting feasibility-related operational risks and mitigation actions for program and trial feasibility and allocation.
+ Leads development of innovative solutions in trial allocation strategic plans to ensure adequate patient accessibility, patient engagement, and alignment with regional and country strategies.
+ Performs ongoing analysis and reassessment of feasibility against recruitment throughout the lifecycle of the trial, including re-allocation or corrective actions when needed.
+ Ensures alignment of feasibility and allocation strategy and seamless start up planning with Global Feasibility Director, in collaboration with teams/associates responsible for regional feasibility.
+ Partnering with Global Health Insights Director(s), builds center of excellence in strategic feasibility and allocation planning by developing process standards and tools to achieve strategic feasibility and allocation excellence in GDO.
+ Drives multidisciplinary taskforces and supports implementation of initiatives to optimize best practices for strategic feasibility to support continuous improvement and other management initiatives.
+ Key contributor and lead for Global Feasibility Management forums, initiatives, or working groups. Serves as faculty member for franchise training programs.
**Ideal background**
+ Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred.
+ Fluent English (oral and written)
+ At least 5 years of pharmaceutical clinical drug development experience recommended (with ≥3 years in planning/execution global clinical trials recommended)
+ Strong understanding of all aspects of clinical drug development with particular emphasis on clinical trial design, trial execution, and strong knowledge about the feasibility and allocation process of a program and/or study.
+ Possess strong, resourceful research skills to locate unusual information and have capacity to develop a deep domain specific knowledge base.
+ Understand the Clinical Trial matrixed process from research through post marketing phase IV, health authority guidelines, country challenges as well as sources for therapeutic area data.
+ Demonstrated ability to collaborate across partner functions in a matrix environment, without direct reports, but able to coordinate the activities of others.
+ Demonstrated experience in feasibility for global clinical trials.
+ Demonstrated ability to navigate in matrix environment.
+ Has experience in or understanding of trial level budgeting.
+ Has coached, mentored, on boarded peers and/or new associates.
+ Has had success in identifying, proactively flagging, and resolving risks; experience with strategic scenario planning and management.
+ Excellent negotiation and conflict resolution skills.
+ Excellent organizational, interpersonal skills with extensive networking expected.
+ Communicates effectively with leaders in a local/regional/global matrixed environment.
+ Proven ability on strategic planning and managing operational challenges at global, regional or country level.
+ Good project management capabilities with demonstrated ability to problem solve and mediate complex issues.
+ Thorough knowledge of the international aspects of drug development process, the international standards (GCP/ICH), health authority regulations, and clinical development process.
+ Good understanding of global competitive landscape and implications on clinical development.
+ Good medical/scientific understanding; ability to translate to business knowledge and trial execution.
+ Good understanding of pharmaceutical industry, key competitors in disease area, commercial strategy integration into clinical trials.
+ Strong leadership and negotiation skills.
+ Demonstrated strong presentation and diplomacy skills.
+ Demonstrated ability to influence without direct authority.
+ Location: EMEA & USA
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled$109k-137k yearly est.60d+ ago
Associate Director - Business Continuity & Disaster Recovery
They will also work together with other members of the IQVIA Information Security team, and liaising regularly with other management teams at IQVIA, including CIO organization, Global and Regional Business Units, and Corporate Functions. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.$109k-137k yearly est.60d+ ago
Associate Director, Epidemiology, Real World Evidence
The Associate Director (AD), Epidemiology, will work in IQVIA's Center for Advanced Evidence Generation, using epidemiological knowledge to drive innovation and research. This individual will lead strategic initiatives across IQVIA, write manuscripts, contribute to proposals, and protocol design. + Serves as key team member in the Center for Advanced Evidence Generation, developing strategy and contributing to leadership initiatives across IQVIA. + Represents IQVIA externally through conference presentations. + Works collaboratively on inter-disciplinary teams, internal and external to IQVIA IQVIA is a leading glo$128k-167k yearly est.60d+ ago
Associate Director - Email Services
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health.$126k-163k yearly est.60d+ ago
Associate Director - Business Continuity & Disaster Recovery
They will also work together with other members of the IQVIA Information Security team, and liaising regularly with other management teams at IQVIA, including CIO organization, Global and Regional Business Units, and Corporate Functions. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.$112k-145k yearly est.60d+ ago
This is an exciting opportunity to be a part of an industry leader and have a significant impact on future growth of our Field Force Operations Center of Excellence The IQVIA FFO CoE empowers our customers to transform HCP engagement through solutions that improve business processes, drive tailored communications, and optimize sales resources. IQVIA offers a range of services and technologies focused on continuous enhancement of HCP engagement as well as the overall HCP experience. Whether planning field force resources, designing & managing complex incentive programs, delivering end-to-end speaker bureau strategy and management, or optimizing every HCP interaction, IQVIA Technologies enable healthcare companies to engage HCPs more effectively. + Present IQVIA's overall value proposition with a specific focus on our portfolio of technology solutions which include: + Act as a liaison between prospect/customer and IQVIA Services and Delivery teams as necessary$112k-145k yearly est.60d+ ago
This is an exciting opportunity to be a part of an industry leader and have a significant impact on future growth of our Field Force Operations Center of Excellence The IQVIA FFO CoE empowers our customers to transform HCP engagement through solutions that improve business processes, drive tailored communications, and optimize sales resources. IQVIA offers a range of services and technologies focused on continuous enhancement of HCP engagement as well as the overall HCP experience. Whether planning field force resources, designing & managing complex incentive programs, delivering end-to-end speaker bureau strategy and management, or optimizing every HCP interaction, IQVIA Technologies enable healthcare companies to engage HCPs more effectively. + Present IQVIA's overall value proposition with a specific focus on our portfolio of technology solutions which include: + Act as a liaison between prospect/customer and IQVIA Services and Delivery teams as necessary$126k-161k yearly est.60d+ ago
Associate Director of Architecture
**Overview** **IQVIA ** is the world's leading company providing information, technology, and services for virtually every type of stakeholder in healthcare. Every day, IQVIA innovates on a large scale. IQVIA stores and computes more than 20 petabytes of complex healthcare data on diseases, treatments, costs and outcomes to enable our clients to run their operations more efficiently. IQVIA employs over 50,000 professionals in over 100 countries to drive results for over 5,000 healthcare clients globally. IQVIA is a publicly listed company (NYSE - Q) with estimated revenue close to $7B and a market cap of over $18B. **IQVIA Commercial Solutions** provides tools to the Life Sciences industry in countries around the world. **Job Summary:** The Associate Director will assist with the conceptualization, development and deployment of an enterprise architecture which supports current and future IQVIA systems, products and platforms and that satisfies business product strategy.$129k-166k yearly est.60d+ ago
