Site Contract Analyst Home-based India As a (Site Contract Analyst) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing Manage and may lead the day-to-day operations within relevant support function to ensure completion per established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordination with key business stakeholders (e.g., study teams) to support timely completion of both drug and non-drug program goals and objectives Manage and may lead functional and cross-functional internal teams Provide accurate and up-to-date project status and financial information (where appropriate) within relevant tracking systems/tools Proactively identify and escalate issues that arise related to support functional deliverables Responsible for implementation of standards for designated functional areas Responsible for the management of functional budgets and resources (where appropriate) and management of related components of trial or support function budgets, timelines and resources. May also provide oversight for these activities. You Are BA/BS degree with ≥3 years of experience in pharmaceutical related drug development or direct equivalent experience Holds more than 5 years in clinical research industry Have more than 3 years of direct site contract & budget negotiation experience Must have knowledge of clinical trial conduct, including, multi-center, global trials. Must have strong knowledge of ICH/GCP guidelines and regulatory requirements. Requires proven project management skills and leadership ability Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Fluent in English. Full Home-Based What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

Senior Statistical Programmer Location: Bangalore-Homebased Skills: R Programming As a Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing Develop understanding of all applicable policies and procedures Completes programming activities under supervision Takes responsibility for timely completion of all assigned development task Understands and applies a basic knowledge of industry standards You Are Having 4+ years of experience in SAS & R Programming Able to lead 1 study under supervision Able to demonstrates strong programming and domain expertise Having ability to execute a wide range of programming activities with minimal supervision. Able to identify gaps in current programming best practices and may offer suggestions Able to ensure adherence to standards and has an awareness of evolving industry standards What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Job Title: Senior Clinical Data Science Programmer Location : Chennai/ Bangalore What You Will Be Doing Strong SQL skills working in the clinical data management environment. In depth knowledge of Visualization Design and good understanding of end-to-end data flow in Data management. Strong technical experience with Data Management Reports and Listings such as Clean Patient Tracker, DM Metrics , coding listings etc. High attention to detail including proven ability to manage multiple, competing priorities. Experience working in a matrix environment and collaborating across functions and organizations, including demonstrated ability to influence without authority. Knowledge of GCP and other regulations. Good knowledge of CDISC, SDTM standards. Excellent written and oral communication skills. Demonstrated leadership, problem solving, conflict resolution, and team building skills. You Are Any life science graduation 5+ Years of experience must Location : Chennai/Bangalore What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

Senior Biostatistician Location: Bangalore, Homebased As a Senior Biostatistician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing Supports design, analysis and interpretation, uses a wide range of statistical approaches and/or applicable software to explore options Authors analysis plans and prepares statistical inputs to key documents and presentation materials Contributes to the development of statistical strategy at a study-level, which may be shared with stakeholders Anticipates problems related to assigned work or areas of expertise and able to implement solutions, proactively seeking input from supervisor/manager You Are Having 5-8 years of experience in SAS and confidence in leading submission Having ability to perform Study Statistician role with minimal supervision Able to demonstrate strong statistical expertise with a good understanding of more complex design of experiments and inference methodologies (where applicable awareness / knowledge of Bayesian, Futility & Predictive Inference, Estimands, Missing Data etc.) Where required, have ability to actively participate in matrix team meetings What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, Job Title: Clinical Data Enablement Data Aggregation Lead Location : Chennai/ Bangalore What You Will Be Doing Enable the data flow for Phase I-IV clinical trials consistent with aligned commitments inclusive of data ingest, transformation and internal availability of this data for data review, data cleaning and readiness for data analysis Works directly with vendors providing source data (i-e vendors providing lab results, ECGs, biomarkers, etc ?) and/or internal functions such as clinical operations or early development to ensure that related specifications, mechanisms for data transfers and data transfer schedules are established and executed appropriately Contributes to related technical and/or process improvement initiatives associated with the clinical results data flow and efforts within the department and across sponsors broadly Collaborates with vendors providing capabilities and/or support for the clinical data flow to ensure successful delivery of study level data Collaborates cross functionally with areas performing data management, clinical operations, IT support, etc to address any issues with the delivery or stability of the clinical data flow as appropriate You Are BS or MS degree, preferably in Computer Science, Informatics/Data Science, or life science discipline Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives Prior experience with systems and processes that include an end-to-end data flow and the transformation of data in support of data review and/or data cleaning Strong verbal and written communication skills What ICON Can Offer You Our success depends on the quality of our people Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent, In addition to your competitive salary, ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers iconplc /benefits At ICON, inclusion & belonging are fundamental to our culture and values Were dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status, https://careers iconplc /reasonable-accommodations Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles,

As a Senior Clinical Transparency Lead you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence, What You Will Be Doing Assesses requirements for clinical trial registration / disclosure of results or public disclosure strategy plans, Prioritizes, oversees, and performs the day-to-day operations of Clinical Transparency or Public Disclosure, ensuring the timely completion, review and approval of registration, updates and results disclosure activities, Manages the review and approval process for clinical trial registrations or public disclosure tracking mechanisms, including communication with partner companies or collaborators, Facilitates periodic review of active registrations or public disclosure strategy plans to ensure records are updated or verified as required, Uses independent judgment to assess clinical transparency or public disclosure activities and problem solving to determine escalation of issues to management, Coordinates and oversees the work of consultants and vendors as applicable, Addresses inquiries related to clinical transparency or public disclosure activities, Provides feedback to Clinical Transparency or Public Disclosure leadership resulting from new and updated transparency requirements, Leads retrospective review to ensure compliance of trials resulting from new clinical transparency or public disclosure knowledge or requirements, Develops training materials, reference documents and tools for use with clinical transparency or public disclosure activities, Educates study or asset team members and other organizational contacts on clinical transparency or public disclosure policies and processes, Establishes and maintains global working relationships, Communicate changes throughout the client organization, Work cross-functionally to improve processes and address changes, Evaluate process automation, systems, and tools to improve efficiency, accuracy, and productivity, Lead clinical transparency or public disclosure training for global colleagues, You Are Bachelors Degree, or equivalent experience required, 5 years pharmaceutical industry experience required with experience in Transparency and/or Disclosure activities Working knowledge of clinical drug development and clinical trial protocols Excellent organizational skills and high attention to detail, Self-directed and motivated, with ability to work without significant direct supervision, asking questions when necessary, Ability to manage multiple tasks and readily switch activities to accommodate priority needs, Proficient computer skills, including experience with MSWord and Excel, Healthcare professional background preferred, What ICON Can Offer You Our success depends on the quality of our people Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent, In addition to your competitive salary, ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers iconplc /benefits At ICON, inclusion & belonging are fundamental to our culture and values Were dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status, If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below, https://careers iconplc /reasonable-accommodations Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles,

ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, Job Title: Senior Lead Clinical Data Science Programmer [Elluminate] Location : Chennai/ Bangalore What You Will Be Doing Develop, implement and maintain date review and data cleaning capabilities for sponsors led Phase I-IV clinical trials using sponsors technologies in support of efficient study execution and related decision-making including incorporation of emerging approaches to such activities Contributes to related technical and/or process improvement initiatives associated with data reporting and analytics across DS and Astellas broadly Collaborates with any vendors providing data reporting and analytical capabilities and/or support for such capabilities Collaborates cross functionally to ensure that any issues with the data reporting and analysis are addressed as appropriate You Are BS or MS degree, preferably in Computer Science, Informatics/Data Science, or life science discipline Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives Prior experience in Reporting [Elluminate or Cluepoint] Strong verbal and written communication skills What ICON Can Offer You Our success depends on the quality of our people Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent, In addition to your competitive salary, ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers iconplc /benefits At ICON, inclusion & belonging are fundamental to our culture and values Were dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status https://careers iconplc /reasonable-accommodations Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles,

ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, Job Title: Senior Clinical Data Science Programmer [ Elluminate] Location : Chennai/ Bangalore What you will be doing: Strong SQL skills working in the clinical data management environment, In depth knowledge of Visualization Design and good understanding of end-to-end data flow in Data management, Strong technical experience with Data Management Reports and Listings such as Clean Patient Tracker, DM Metrics , coding listings etc High attention to detail including proven ability to manage multiple, competing priorities, Experience working in a matrix environment and collaborating across functions and organizations, including demonstrated ability to influence without authority, Knowledge of GCP and other regulations Good knowledge of CDISC, SDTM standards, Excellent written and oral communication skills Demonstrated leadership, problem solving, conflict resolution, and team building skills, Required Skills Elluminate desired, Spotfire, Qlik , Tableau, working in the biotechnology or pharmaceutical industry, You are: Any life science graduation 5+ Years of experience must Location : Chennai/Bangalore What ICON Can Offer You Our success depends on the quality of our people Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent, In addition to your competitive salary, ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers iconplc /benefits At ICON, diversity, inclusion & belonging are fundamental to our culture and values Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities We're proud of our diverse workforce and the work weve done to become a more inclusive organisation Were dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below, https://careers iconplc /reasonable-accommodations Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles,

ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, Job Title: Principal Clinical Data Science Lead Location : Bangalore/Remote What You Will Be Doing Oversees the collection of all clinical trial data from multiple sources, Very strong subject matter expertise in the Data Manageement (DM) discipline Can support multiple studies concurrently with little to no oversight by functional manager, Performs DM vendor oversight activities across multiple studies Reviews and gives input in vendor oversight processes, Review Key Risk Indicators (KRIs) outputs in aggregate across sites, regions and countries As needed, review study level operational and patient data to support the investigation and root cause analysis of observations, Provides training and subject matter expertise to lower-level DM peers, Collaborate with clinical operations, investigators, and other stakeholders to ensure smooth data flow throughout the trial, You Are BS/BA degree in a biological science, health-related or computer science field Strong computer skills, including database management software, reporting tools, medical coding tools, and solid understanding of Central Monitoring tools etc Strong understanding of different types of data sources in a clinical trial setting and/or expertise with external data types, Generally, 8 plus years related experience in pharmaceutical, clinical research or health services industry with a minimum of 6 yearsexperience as Data Manager with progressive levels of responsibility, What ICON Can Offer You Our success depends on the quality of our people Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent, In addition to your competitive salary, ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers iconplc /benefits At ICON, inclusion & belonging are fundamental to our culture and values Were dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status, https://careers iconplc /reasonable-accommodations Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles,

The role involves being a Senior Lead clinical data science programmer in the Clinical Data Management area, focusing on enhancing data review and cleaning processes with innovative reports It entails creating and implementing studyspecific data validation procedures and reports, managing the connection to varied data sources, and ensuring efficient scheduling, monitoring, and maintenance on the Clinical Data platform The role requires detailing key handling requirements for scalable data management methods, and deriving study-specific monitoring and validati reports based on clinical protocols and amendments Ultimately, this position aims to advance clinical data management and informatics by improving data integrity, efficiency, and capacity for expansion, Engage closely with Global Development business units such as BDM, Safety, Precision Medicine, Pharmacometrics, Digital Health to deeply understand data quality, monitoring and validation needs and transform these insights into detailed business requirements for clinical data products, Act as the primary point of accountability, responsibility, and expertise in interpreting Clinical Data business needs, meticulously translating and documenting these into comprehensive business specifications at the segment, modality, and company-wide levels, Demonstrates a business understanding of study specific data to identify and assist in successful application of consistent data management processes and documentation across assigned programs, e , ensuring consistency across data quality plans, Thoroughly document the clinical product development process, including data sources, methodologies, algorithms, and underlying assumptions, to guarantee transparency, reproducibility, and auditability of clinical data products, Craft study-specific Data Quality specifications and define key Clinical data metrics to uphold the highest data quality and integrity standards across study lifecycles, Prepare study-level reports within the Clinical Data Platform to support stakeholder activities and ensure the effective use of clinical study data, Query small to large clinical data sets, manage data ingestion and delivery specifications, and data modeling requirements analyzes and evaluates clinical data, recognizes inconsistencies, and initiates the resolution of da Design clear, concise requirements for clinical reports and dashboards, establishing relevant metrics to convey data-driven insights Present findings in a compelling manner, customized for key clinical business functions such as Clinical Data Management, Pharmacometrics, Precision Medicine, etc Work towards preparing Common Data Model mapping & transformations to ensure data is usable in the analytical layer/ and comply with the Governance Committee strategy, Have hands-on experience with various clinical datasets such as EDC and non-crf dat combined with strong analytical abilities capable of managing diverse, large, and complex datasets, which ranges from fundamental research collections to detailed clinical information, Possess a deep understanding of modern data analytic frameworks and technology, which includes expertise in Big Data structures, Lakehouse architectures, as well as contemporary techniques for data collection and amalgamation, Have full understanding of clinical trial Have a passion for championing and implementing clinical data Should have practical experience with ETL processes, programming languages such SQL, Python, R, and familiarity with the AWS cloud infrastructure, including S3, Da Lake, along with analytics realms Have strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and Possess Excellent communication, and project management skills, Have a bachelors degree in computer science, Data Science, Statistics, or a similar area is required Candidate should have substantial experience, ideally over 7 years, specifically within clinical data analysis and preferab within the BioPharma sector Important Information For Applicants This role does not offer remote work and is not open to freshers, Please review the job description carefully before applying,

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are seeking a highly experienced Clinical Trial Risk Management Specialist with a strong pharmaceutical industry background. The ideal candidate will possess extensive expertise in clinical trial development, risk management, and monitoring processes, with a proven track record in managing complex clinical studies within a global matrix environment. Key Responsibilities Lead and oversee clinical trial risk management activities, including identification, assessment, and mitigation of study-related risks throughout the clinical trial lifecycle. Utilize strong clinical and monitoring experience (central and site) to ensure high-quality data collection, analysis, and reporting. Conduct clinical data analytics to identify risk signals, trends, and outliers to proactively manage and mitigate trial risks. Collaborate cross-functionally across global and country teams to ensure alignment with clinical development strategies and compliance with international regulations and company standards. Apply expert knowledge of international standards (GCP, ICH), health authority requirements, and organizational policies to support global drug development. Leverage advanced digital tools, e-databases, and risk-based monitoring platforms to enhance trial oversight and reporting. Manage timelines and deliverables effectively, demonstrating strong project management skills. Foster an inclusive and collaborative team environment by recognizing diverse talents, working styles, and cultural contexts. Support transformation initiatives by integrating AI and advanced analytics into clinical trial processes. Provide subject matter expertise in specific therapeutic areas as required. You Are Minimum of 5 years of recent experience in the pharmaceutical industry, including clinical research within pharmaceutical companies or CROs. At least 3 years of comprehensive experience in clinical monitoring (central and/or site), clinical data analytics, data management, or related fields. Experience Working in Cluepoint Deep understanding of the clinical trial management process, including protocol interpretation, study risk assessment, and risk management methodologies. In-depth knowledge of global drug development processes, regulatory environments, and industry best practices. Demonstrated critical thinking and analytical skills with the ability to interpret complex clinical data and drive actionable insights. Strong communication, coordination, and stakeholder management skills. Proven ability to work effectively within a global, matrixed organizational structure. Proficiency in using digital clinical tools and analytics platforms. Experience in project management with a track record of delivering projects on time. Awareness of team dynamics and experience fostering collaborative, high-performing teams. Experience in clinical trial transformation efforts, including AI and analytics integration. Ability to navigate diverse cultural environments and promote inclusion. What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

Home-based, Location: Chennai As a Clinical Research Associat e you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives. What You Will Be Doing Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock. You will be embedded in our client's study team and have a dedicated ICON line manager to support you Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports Support and mentor other team members Qualification Education: B.Pharm/M.Pharm/Pharm D/BDS/MBBS Minimum 2 years of onsite monitoring (excluding any training & induction) of Oncology Strong & clear communication skills Location: Chennai. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Show more Show less

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Job Title: TMF Specialist II/III Location : Bangalore What You Will Be Doing Performs Quality Check and indexing of TMF documents for in-house studies. Supports compilation of the TMF Management Plan and TMF Index in association with the TMF Owner and CROs. Ensures that documentation flow for Trial Master File documents meets the required timelines and intervenes with action plans and follow up as appropriate. Prepares and participates in audits/inspections to ensure ongoing readiness of the TMF; assists with responses about documentation management activities for audits, questions, and issues. Provides regular feedback to the Project Team on TMF status, including actionable metrics. Whenever necessary, provides re-training to the Project Team. Manages study setup in the eTMF System on a timely basis for studies assigned and communicate same to end users. Performs CRO TMF completeness review for metadata checks and targeted missing items according to each CRO’s TMF Plan and TMF Index. You Are Bachelor’s degree in life sciences, clinical research, or a related field. Extensive experience in TMF management or clinical operations within the pharmaceutical or clinical research industry. Strong understanding of GCP, ICH guidelines, and global regulatory requirements related to TMF management and clinical trial documentation. What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

As a (Senior Contract Analyst) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing Manage and may lead the day-to-day operations within relevant support function to ensure completion per established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordination with key business stakeholders (e.g., study teams) to support timely completion of both drug and non-drug program goals and objectives Manage and may lead functional and cross-functional internal teams Provide accurate and up-to-date project status and financial information (where appropriate) within relevant tracking systems/tools Proactively identify and escalate issues that arise related to support functional deliverables Responsible for implementation of standards for designated functional areas Responsible for the management of functional budgets and resources (where appropriate) and management of related components of trial or support function budgets, timelines and resources. May also provide oversight for these activities. You Are BA/BS degree with ≥3 years of experience in pharmaceutical related drug development or direct equivalent experience Holds more than 5 years in clinical research industry Have more than 3 years of direct site contract & budget negotiation experience Must have knowledge of clinical trial conduct, including, multi-center, global trials. Must have strong knowledge of ICH/GCP guidelines and regulatory requirements. Requires proven project management skills and leadership ability Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Fluent in English. Full Home-Based What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

As a Clinical Research Associat e you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives. What you will be doing: Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock. You will be embedded in our client's study team and have a dedicated ICON line manager to support you Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports Support and mentor other team members Qualification: Education: B.Pharm/M.Pharm/Pharm D/BDS/MBBS Minimum 2 years of onsite monitoring (excluding any training & induction) of Oncology Strong & clear communication skills Location: Chennai. Show more Show less

As a Technical Application Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing Collaborate with the Business & technology collaborators to gather requirements to implement the product vision balancing with technical feasibility. Shape and prioritize backlog, utilize business expertise and understanding of customer needs to translate requirements into user stories with define acceptance criteria. Facilitate release planning, sprint planning and demos with Stakeholders. Manage technical debt, optimize cost, and improve delivery efficiency. Define and lead all aspects of the overall engineering and technology architecture, roadmap, and technical decisions, using modern design patterns and architectural principles for the product needs in coordination with the Technical Product Manager, Product Group Lead Engineer, and Business Unit Architect. Ensure the product/systems meet relevant security, privacy & compliance standards. Work collaboratively with diverse internal and external (vendor) teams to ensure smooth transitions and minimal operational disruptions. Actively engage in build activities while supporting system architecture /design/code reviews; facilitate technical challenge problem-solving within the squad using the technology strategy as a guide. Closely follow up with the application support teams on incident tickets, problem tickets and requests. Make sure pending tickets are being resolved within the defined SLA’s Communicate status and resolution notes to business stakeholders on a timely manner. Escalate ticket resolution when appropriate Coordinate technical deep-dive and troubleshooting sessions with application support teams Lead validated implementation of product systems according to SDLC You Are Bachelor’s degree or equivalent and a minimum of 8 years of relevant experience OR advanced degree or equivalent and a minimum of 6 years of relevant experience is required. Experience with clinical trial technology and information systems, projects and processes are highly preferred. Project Management Certification is preferred Effectively manage internal and external business partner relationships in support of R&D deliverables Technical expertise in: SAS, Python, Java, JIRA, AWS and Azure Knowledge of Clinical Pharmacology systems such as NONMEM, Phoenix, NCA-systems, R, Altair/Grid computing experience, Matlab, MRGSolve and Monolix and system/data integrations for analytics, compliance, and dashboarding Understanding of AI/ML concepts within a pharmaceutical business environment What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

As a Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Skills required: R & SQL What You Will Be Doing Identifies gaps in current programming best practices and may offer suggestions Ensures adherence to standards and has an awareness of evolving industry standards Demonstrates strong programming and domain expertise. Able to lead 1 study under supervision You Are Proficient in R and SQL programming Expertise in Oncology databases such as Flatiron, COTA Has good understanding of Oncology specific analyses such as Line of Therapy algorithms, Survival analysis, different statistical models Preferable to have R Shiny or Instant Health Data (IHD) experience Experience with Analytic Datasets, patient cohorts is good to have What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

As a Medical Coding Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Location: Remote Shift: 2pm-11pm IST What You Will Be Doing Coding performed in accordance with departmental coding conventions and company SOPs. The coder will generate queries for clarification of potentially discrepant data. Ability to work in cross-functional team-oriented environments. Assist with data coding consistency reviews and SAE reconciliation, as needed. The Coder will collaborate with medical monitors, Clinical and Data Management team members, as required, to ensure the timely processing of coding, according to project timelines. You Are 5+ years of experience as medical coder Experience with MedDRA and WHODD required. Experience with set-up activities Dictionary up version Medidata Rave experience ATC coding experience Working knowledge of medical terminology, clinical trials & coding is essential. What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Job Title: Principal Clinical Data Science Programmer [Elluminate] Location : Bangalore/Remote What You Will Be Doing Develop, implement and maintain date review and data cleaning capabilities for sponsors led Phase I-IV clinical trials using sponsors technologies in support of efficient study execution and related decision-making including incorporation of emerging approaches to such activities Contributes to related technical and/or process improvement initiatives associated with data reporting and analytics across DS Collaborates with any vendors providing data reporting and analytical capabilities and/or support for such capabilities Collaborates cross functionally to ensure that any issues with the data reporting and analysis are addressed as appropriate You Are BS or MS degree, preferably in Computer Science, Informatics/Data Science, or life science discipline Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives Prior experience in Reporting [Elluminate or Cluepoint] Strong verbal and written communication skills What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less

Data Scientist Location: Bangalore, India [Officebased - hybrid model] As a Data Scientist , you will be fully dedicated to one of our global pharmaceutical partners—a company renowned for performance, innovation, and quality. This role offers the best of both worlds: the stability and support of a top CRO and the agility of a pharma environment that values innovation and individuality. You will play a key role in driving data-driven decision-making across the business by contributing to the strategy and execution of analytics, metrics, and visualization solutions. This includes developing models, building automated tools, and delivering actionable insights across clinical and business domains. What You Will Be Doing Coordinate with different functional teams to implement models and monitor outcomes. Develop processes and tools to monitor and analyze model performance and data accuracy. Leveraging business intelligence tools i.e Spotfire for analysis and review. Develop custom data models and algorithms to apply to data sets. Providing specialist support for development, interpretation and application of machine learning models Applying analytical and statistical methods to solve identified use cases in an agile manner using various data sources and analytical tools Work with key stakeholders throughout the organization to identify opportunities for leveraging company data to drive business solutions. Liaising, advising and negotiating with key customer groups on requirements and proposing innovative solutions to meet their data modelling requirements Responsible for the development and implementation of capabilities to make provisioning of routine requests more routine, structured and efficient Contributing to initiatives that enable faster and more effective data modelling/analysis and provisioning Ensuring systems and code, documentation are inspection ready You Are A solutions orientated, analytical and customer focused individual with a global business mind set and a strong background in operational excellence! Here At ICON We Want Our Employees To Succeed And Ensure That They Are Set Up For This Success Through Constant Training, Development And Support. To Enable Success In This Position You Will Have We’re looking for someone with 3-5 years of experience manipulating data sets and building statistical models, has a Master’s or PHD in Statistics, Mathematics, Computer Science. Experience using statistical computer languages Python & SQL (R Considered) to manipulate data and draw insights from large data sets. Experience working with and creating data architectures. Experience of clinical data and domains (Experience working within Clinical Trials or the wider Pharmaceutical industry) preferable but not necessary Knowledge of a variety of machine learning techniques (clustering, decision tree learning, artificial neural networks, etc.) and their real-world advantages/drawbacks. Knowledge of advanced statistical techniques and concepts (regression, properties of distributions, statistical tests and proper usage, etc.) and experience with applications. Excellent written and verbal communication skills for coordinating across teams. A drive to learn and master new technologies and techniques What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Show more Show less