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IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to ...
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About The Job
Job Overview
- Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field.
- Identifies and elevates potential new business opportunities and assists in the sales process.
Essential Functions:
- Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects.
- Reviews and analyzes client requirements or problems and assists in the development of proposals of cost effective solutions that ensure profitability and high client satisfaction.
- Provides direction and guidance to Analysts, Consultants, and where relevant, to Statistical Services assigned to engagement.
- Develops detailed documentation and specifications.
- Performs qualitative and/or quantitative analyses to assist in the identification of client issues and the development of client specific solutions.
- Designs, structures and delivers client reports and presentations that are appropriate to the characteristics or needs of the audience.
- May deliver some findings to clients.
- Recommends improvements and alternative solutions to resolve problems.
- May identify new business opportunities of follow-on work and new leads at assigned client.
- Provides follow-up with client after project deliverable has been completed to ensure client satisfaction.
- Proactively develops broader and deeper knowledge of related consulting methodologies and life sciences market through on the job experience and participation in training opportunities. Begins to develop CoE specific subject matter expertise.
- When acting as Project Manager, proactively manages project timelines and manages day to day communication with the client and team members.
Qualifications:
Bachelor's Degree Req
- Master's Degree Business Administration Pref
- 5-8 years of related experience in consulting and/or life sciences industry Req
- Possesses solid project management skills and client influencing and relationship building skills.
- Works willingly and effectively with others in and across the organization to accomplish team goals.
- Experienced with developing consultative relationships with senior level managers and executives at clients in the life science industry.
- Ability to manage multiple projects, juggle priorities and deliver on tight deadlines.
- Knowledge of consulting methodologies, tools and techniques related to functional area.
- Knowledge of key issues and current developments in the life science industry.
- Excellent presentation, communication and client influencing skills.
- Has established network and referral contacts.
- Has necessary subject matter expertise to effectively manage projects within a given CoE.
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About The Job
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.
- You will have the opportunity to work globally and across a variety of therapeutic areas.
- IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.
Job Overview:
- As a Manager for the Biostatistics department, you will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying statistical methods to project work.
- With site/staff level of visibility, you will manage a team of Biostatistics staff and provide training, guidance, and mentorship to staff members.
- Along, with communicating on project progress, staffing concerns, including resource allocation with the Director, Biostatistics
- You will perform expert reviews and participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.
Requirements:
- BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience in supervising/managing staff
- Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials
- In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Familiarity with moderately complex statistical methods that apply to applicable clinical trials
- Strong working knowledge of SAS
- From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.
What is in it for you:
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance
go to method of application »
About The Job
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.
- You will have the opportunity to work globally and across a variety of therapeutic areas.
- IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.
Job Overview:
- As a Biostatistician 2, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
- Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.
- You will develop statistical methods sections of protocols and review case report forms (CRFs), coupled with, preparing analysis plans, and writing specifications for analysis files, consistency checks, tables, and figures.
- Along with, communicating with clients regarding study protocol or statistical analysis issues as they arise and interpreting analyses and writing statistical sections of study reports.
- Acting as a lead on studies, you will train and mentor staff and manage scope of work and budget and provide revenue and resource forecasts for single studies.
Requirements:
- BSc or MSc degree in Biostatistics or related field, and 2-4 years’ relevant experience within the life-science industry
- Familiarity with moderately complex statistical methods that apply to applicable clinical trials
- Good working knowledge of SAS and CDISC
- Ability to effectively manage multiple tasks and projects.
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About The Job
IQVIA’s Gastroenterology, Immunology and Women’s Health Unit is a global team of professionals dedicated to assisting our clients in driving healthcare forward and enabling medical breakthroughs that advance healthcare and patient treatment options around the world.
We are looking for a Senior Project Leader with experience in Gastroenterology, Autoimmune and Rheumatology, Dermatology, Rare Diseases, Plasma Derived Therapies or Women’s Health experience to join our innovative and dynamic group.
- As Senior Project Leader you will manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control.
- You will be supported by domain experts in every function, enabled by best-in-class technology and data analytics.
- Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager as an expert in start-up.
- This is an important and high-profile role within our Research & Development Operation and IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.
Typically assigned to one or two projects, or a program, responsibilities might include:
- Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope
- Serving as the primary contact with the customer for progress and governance
- Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures
- Anticipating risk and implementing mitigation strategies
- Managing study team assignments, accountability and resource requirements
- Ensuring the study budget is managed proactively including scope changes and financial systems are accurate
Required Knowledge, Skills And Abilities:
- Bachelor's degree in life sciences or related field
- Global project management experience within the drug development industry, with previous CRO experience is ideal
- Minimum 4 years prior project management experience and experience in clinical operations; or equivalent combination of education, training and experience
- In depth therapeutic knowledge in Gastroenterology (Irritable Bowel Disease, Pancreatitis, Ulcerative Colitis, Crohn’s Disease, Non-alcoholic steatohepatitis (NASH), Gastroesophageal Reflux Disease (GERD)), Autoimmune/Rheumatology (RA, Lupus or Osteoarthritis), Dermatology (Psoriasis, Atopic Dermatitis or Urticaria) ), Rare Diseases Plasma Derived Therapies, or Women’s Health (including Fertility; Contraception; Endometriosis, Osteoporosis) would be an advantage
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About The Job
This is a brilliant opportunity for an established Statistical Programmer 2 to join an exceptional and dynamic programming group. We seek someone willing to move from one Statistical Programmer 2 role to another in return for the experience and unrivalled career progression Iqvia can offer. We ask you only apply if you match or exceed the candidate criteria below.
Job Overview:
- As a Statistical Programmer 2, you will provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.
- You will plan and lead the development of project-related solutions to the full scope of statistical programming tasks.
- As a lead programmer on assigned studies, you will write and maintain programming specifications datasets and program TLFs, to maximize programming efficiency with the use of biostatistical tools and assist in training and mentoring new or junior team members
Essential Candidate Requirements:
- Bachelors or Masters’ in Computer Science, Mathematics or equivalent
- 3+ years, statistical programming experience within the Life Science industry in SAS
- Experience as project lead, directly engaging clients and coordinating tasks within a programming team
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
- Ability to independently lead multiple tasks and projects
go to method of application »
About The Job
We are looking for Project Leader/ Senior Project Leader’s to join our innovative and dynamic group of global professionals dedicated to assisting our clients in driving healthcare forward.
- This is an important and high-profile role within our Research & Development Operation business unit to enable medical breakthroughs that advance healthcare and patient treatment options around the world.
- As Project Leader/ Senior Project Leader you will liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will manage cross functional teams across this global organization and be supported by domain experts in every function, enabled by best-in-class technology and data analytics.
Typically assigned to one or two projects, or a program, responsibilities might include:
- Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope
- Serving as the primary contact with the customer for progress and governance
- Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures
- Anticipating risk and implementing mitigation strategies
- Managing study team assignments, accountability and resource requirements
- Ensuring the study budget is managed proactively including scope changes and financial systems are accurate
Required Knowledge, Skills And Abilities:
- Bachelor's degree in life sciences or related field
- Global project management experience within the drug development industry, with previous CRO experience is ideal
- Minimum 2-4 years prior project management experience and experience in clinical operations; or equivalent combination of education, training and experience
- In-depth therapeutic knowledge in one of our key therapeutic areas including: Internal Medicine, Central Nervous System, Gastroenterology, Immunology & Women’s Heath, Cardiovascular Renal Metabolic, Early Clinical Development or Oncology
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About The Job
The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.
We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department. You will have the opportunity to work globally and across a variety of therapeutic areas.
IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.
Job Overview:
As a Senior Statistical Programmer, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.
- You will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients’ needs.
- You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
- Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. As well as, estimating programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.
Requirements:
- Bachelors or Masters’ in Computer Science, Mathematics or equivalent
- 5+ years Statistical Programming experience within the Life-Science industry
- Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
- Excellent knowledge of CDISC standards (SDTM and ADaM)
- Excellent application development skills
- Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
- Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
- In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
- (GCP) and International Conference on Harmonization (ICH) guidelines
- From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.
What is in it for you?
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance
go to method of application »
About The Job
Job Overview:
As a Statistical Programming Scientist/Principal, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.
- You will also provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies.
- This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
- You will provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
Requirements:
- Bachelors or Masters’ in Computer Science, Mathematics or equivalent
- 7+ years’ Statistical Programming experience within the Life-Science Industry
- Advanced knowledge of statistics, programming and/or clinical drug development process
- Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro language
- Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)
- From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.
What is in it for you?
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance
Method of Application
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