Senior Lead Clinical Data Science Programmer Job at iconplc

Senior Clinical Python Programmer

Sr Clinical Programmer (Phyton) - Mexico - Remote. ICON plc is a world-leading h...

Location

Mexico , Mexico City

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Degree in Data Science, Statistics, Computer Science, or a related field
advanced certifications in data programming or clinical data science are advantageous
extensive experience in clinical data programming, with a strong background in statistical analysis, data management, and programming languages such as SAS, R, or Python
proven ability to lead and manage programming teams, and develop data science solutions that support clinical research objectives
strong analytical skills, with experience in designing and implementing complex data analysis and visualization techniques
excellent communication and leadership skills, with the ability to collaborate effectively with cross-functional teams and present data insights to stakeholders
willingness to travel as required (approximately 10%)

Job Responsibility

Leading the design, development, and validation of data science programming solutions to support clinical trials, including data integration, statistical analysis, and reporting
managing and mentoring a team of clinical data programmers, providing guidance and ensuring adherence to programming standards and best practices
collaborating with clinical research teams and stakeholders to define data requirements, develop programming specifications, and implement data science methodologies
overseeing data quality assurance processes, including data validation and verification, to ensure the accuracy and completeness of clinical trial data
utilizing advanced statistical techniques and data visualization tools to analyze complex data sets and generate actionable insights for clinical research
staying current with industry trends and advancements in data science and clinical research, and recommending innovative solutions to enhance data analysis and reporting

What we offer

Various annual leave entitlements
a range of health insurance offerings to suit you and your family’s needs
competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others

Fulltime

Senior Clinical Database Programmer

The Senior Clinical Database Programmer is responsible for the programming of hi...

Location

India , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor's degree in Life Science, Computer Science or equivalent
Minimum of 5 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
Technical skills and experience using relational databases (e.g. Oracle InForm, Rave EDC System, Oracle DMW, MS SQL Server or MS Access)
Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills
Rave Custom Function Programming skills are mandatory
Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)
Understanding regulatory requirements and relevant data standards
CDISC knowledge and experience are preferable

Job Responsibility

Works closely with department roles and cross-functional study team members to create data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans
Complies with applicable SOPs and work practices
Serves as subject matter expert in one or more technologies
Leads and contributes to cross-functional technical initiatives in collaboration with clients Digital and other teams
Supports knowledge development of data capture tools and methods that support the accuracy and integrity of study data

Senior Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...

Location

Poland , Warsaw

Salary:

200000.00 - 278000.00 PLN / Year

Parexel

Expiration Date

Until further notice

Requirements

Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
Proficiency in SAS
Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
Demonstrated proficiency in analytical programming
Have in-depth understanding of clinical data structure (e.g., CDISC standards) and relational databases
Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
Have good understanding of regulatory, industry, and technology standards and requirements
Have good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs

Job Responsibility

Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
Perform programming validation to ensure quality of analysis datasets and programming outputs
Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
Support the electronic submission preparation and review
Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
Assesses impact on programming activities
Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors
Independently leads and / or performs programming assignments with minimal supervision

What we offer

Fully flexible work arrangement
Opportunity to use Warsaw office if desired
Annual performance-based bonus plan (for eligible roles)
Annual salary review
Total rewards incentives
Extensive training, mentoring, and technical knowledge sharing
Opportunities for career growth
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced technology

Fulltime

Senior Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...

Location

Serbia; Poland

Salary:

200000.00 - 278000.00 PLN / Year

Parexel

Expiration Date

Until further notice

Requirements

Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
Proficiency in SAS
Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
Demonstrated proficiency in analytical programming
Have in-depth understanding of clinical data structure (e.g., CDISC standards) and relational databases
Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
Have good understanding of regulatory, industry, and technology standards and requirements
Have good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs

Job Responsibility

Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
Perform programming validation to ensure quality of analysis datasets and programming outputs
Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
Support the electronic submission preparation and review
Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
Assesses impact on programming activities
Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors
Independently leads and / or performs programming assignments with minimal supervision

What we offer

Fully flexible work arrangement - you can be fully home based
Annual performance-based bonus plan
Annual salary review
Total rewards incentives
Extensive training, mentoring, and technical knowledge sharing
Opportunities for career growth
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Senior Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...

Location

Hungary , Budapest

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
Proficiency in SAS
Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
Demonstrated proficiency in analytical programming
In-depth understanding of clinical data structure (e.g., CDISC standards) and relational database
Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
Good understanding of regulatory, industry, and technology standards and requirements
Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs

Job Responsibility

Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
Perform programming validation to ensure quality of analysis datasets and programming outputs
Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
Support the electronic submission preparation and review
Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
Assesses impact on programming activities
Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors
Independently leads and / or performs programming assignments with minimal supervision

What we offer

Competitive financial packages
Training and development
Healthy work/life balance
Fully flexible work arrangement
Remote, in-office and hybrid roles
Smooth induction and training program
Fertile environment for growth with training programs, mentoring, and knowledge sharing
Diverse therapeutic areas and project exposure
Advanced Technology
Supportive and inclusive environment

Fulltime

Senior Director Translational Data Sciences

We are seeking an exceptional and ambitious scientific leader to serve as Senior...

Location

United Kingdom; Germany; United States , Stevenage; Heidelberg; Collegeville

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Physical sciences (Maths, Computer Science, Physics, Chemistry, Engineering etc) or Biological sciences (Biology, Biochemistry, Bioengineering etc) undergraduate degree or Medical degree
PhD in data science, computer science, computational biology, bioinformatics, or a closely related discipline
Extensive experience spanning academic and industrial drug discovery environments, with a demonstrable record of leading high-impact computational biology programmes from conception through to application to drug discovery or development challenges
Prior line management experience and experience building and leading interdisciplinary teams across computational, experimental, and translational disciplines in both academic and industrial settings
Demonstrated experience structuring and managing strategic partnerships with academic institutions and companies, including contribution to alliance governance
Familiarity with the translational interface between target biology and clinical development
experience with adaptive clinical trial design and biomarker-driven patient stratification is highly desirable
Experience presenting to executive leadership, external partners, and international scientific audiences

Job Responsibility

Scientific Strategy: Develop and execute the Translational Data Sciences strategy, with accountability for portfolio-level outcomes across multiple therapeutic areas including respiratory, renal, hepatology, and immune-mediated disease
Data Sciences and AI: Leverage the potential of data sciences for pipeline progress through team leadership, collaboration across Translational & Developmental Sciences and application across therapy areas and the broader organisations across GSK including R&D Technologies and AIML
Partnership & Alliance Leadership: Establish and maintain high-value partnerships with leading academic laboratories, companies, and international consortia
Translational Integration: Work directly with R&D leadership to align computational strategy with clinical development priorities
Team Leadership: Build and mentor an interdisciplinary team of computational biologists, AI/ML engineers, and clinician-scientists and wet-lab scientists
Scientific Visibility: Contribute to the organisation's external positioning through publications, conference presentations, and academic collaborations

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Head of Majors, Customer Success

Location

United Kingdom , London

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Experience in pharmaceutical, life sciences, medical devices industry
Significant senior leadership experience in Customer Success, Account Management or Strategic Accounts within a B2B SaaS, data, analytics or consulting business serving the pharmaceutical industry
Domain knowledge of the global pharma sector — including R&D, clinical development, commercial strategy, market access and competitive intelligence — with credibility in front of senior pharma stakeholders
Demonstrable track record of owning multi-million-pound/dollar ARR portfolios, delivering against NRR, GRR and churn targets in complex, multi-stakeholder enterprise accounts
Proven success leading, scaling and developing CS teams, including hiring, performance management and embedding competency and incentive frameworks
Strong commercial acumen with the ability to translate client outcomes into renewal and expansion revenue, and to build board-ready narratives supported by data
Excellent executive communication skills, comfortable presenting to and influencing C-suite stakeholders both internally and across global pharma clients
Experience operating within or leading transformation programmes (target operating models, segmentation redesign, churn programmes, customer journey redesign)
Right to work in the UK and ability to work from our London office on a hybrid basis

Job Responsibility

Own renewal rate targets across the Majors portfolio, with full accountability for the renewal pipeline and at-risk book
Partner with Sales and Commercial Operations to identify and convert white-space expansion opportunities across our healthcare product suite
Lead executive-level account planning, QBRs and steering committees with C-suite and senior R&D, commercial and CI stakeholders inside global pharma
Lead, coach and develop a team of Senior CSMs and CSMs covering Top 75 and other strategic accounts
raise the bar on pharma domain expertise and consultative engagement
Embed the CS competency framework, leaderboard and bonus model (VRR, Volume Renewal Rate and LOR-based) across the Majors team to drive performance and accountability
Define and deliver a best-in-class customer journey for the Majors segment, from onboarding through value realisation, advocacy and renewal
Lead execution of strategic programmes including re-onboarding sprints, churn defence and Voice of Customer initiatives within the Majors book
Act as the senior voice of the Majors customer inside GlobalData Healthcare, feeding insight into Product, Analyst, Marketing and Consulting leadership
Partner with the Head of Global CS to shape the 2–3 year CS vision in the context of AI disruption in pharma intelligence

Fulltime

SERM Scientific Director

Provides advanced scientific expertise in the safety evaluation and risk managem...

Location

United Kingdom , London

Salary:

111750.00 - 186250.00 EUR / Year

GSK

Expiration Date

Until further notice

Requirements

Degree in a health-related discipline (e.g., Life Sciences, Pharmacy, Medicine, Nursing), with significant relevant experience
Substantial experience in pharmacovigilance, drug safety, or a related function within the pharmaceutical or biotechnology industry
Experience supporting safety in oncology clinical development programmes
Strong expertise in: Signal detection and risk assessment
Clinical trial safety oversight
Regulatory safety documentation and submissions
Knowledge of global pharmacovigilance regulations (e.g., ICH, GVP, CIOMS)
Proven ability to work effectively in a complex, global matrix environment
Strong analytical, communication, and problem-solving skills

Job Responsibility

Lead pharmacovigilance activities and risk mitigation strategies for assigned oncology assets and clinical trials
Drive the evaluation and interpretation of safety data, including signal detection and assessment
Develop strategic approaches for safety issue evaluation within clinical development programmes
Contribute to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs)
Perform literature review, clinical data synthesis, and integrated safety analyses to inform decision-making
Ensure high-quality, timely delivery while managing multiple priorities
Represent Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams
Lead cross-functional efforts to address urgent and complex product safety issues
Partner closely with Safety Physicians and stakeholders to prepare for and contribute to Safety Review Team (SRT) meetings
Escalate emerging safety issues to senior leadership and governance bodies as appropriate

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Eligibility to participate in our share based long term incentive program

Fulltime

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Senior Lead Clinical Data Science Programmer

Job Description

Job Responsibility

Requirements

What we offer

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