Data Manager, Clinical Data Sciences Job at Pfizer (Buenos Aires)

Manager, Central Monitor, Data Surveillance, Clinical Data Sciences

As part of the Clinical Data Sciences (CDS) group, an integral delivery unit wit...

Location

India , Chennai

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor’s degree or above in a scientific or business related discipline required
Technical expertise and business experience in supporting clinical trials database development, data management, site monitoring, etc.
Thorough understanding of the processes associated with clinical study management, data management, and regulatory operations
Project management skills and technical capabilities as well as effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization
Works independently, receives instruction primarily on unusual situations
Ability to organize tasks, time and priorities
ability to multi-task
Ability to communicate effectively and appropriately with internal & external stakeholders, locally and globally

Job Responsibility

Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables
Provide technical expertise to set up and test study level Risk-based Monitoring system
Review study level system outputs to process for the signal and action management
Plan and execute communication plans & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a study
Able to resolve conflicts, influence and communicate cross-functionally with key stakeholders and customers
Set up and test RBM system at study level to ensure system quality
Define key risk indicators (KRIs) in study system, and ensure consistency between the standard level and the study level
Ensure RBM system alignment with the protocol and adherence to ICH GCP, SOPs, corporate standards and regulatory requirements
Work with Study Team to define the issue resolution for the review of findings as signals and actions
Develop, implement and maintain Quality Control related documentation for RBM related activities to ensure data completeness and accuracy

Fulltime

Director, Group Lead, Data Surveillance, Clinical Data Sciences

As part of the Clinical Data Sciences group, an integral delivery unit within th...

Location

India , Chennai

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor’s Degree. Degree in Life Sciences, Informatics, Computer Science, Statistics, or related business degree with equivalent experience preferred
Demonstrated relevant experience in a pharmaceutical, biotech, Contract Research Organization (CRO), or Regulatory Agency with an emphasis on building data collection and assimilation solutions
Demonstrated experience managing complex projects and developing successful partnerships within and across functional areas
Demonstrated successful experience in all relevant clinical trial activities in a Bio Pharmaceutical or CRO setting
Working knowledge of all phases of clinical trials and multiple indications and/or therapeutic areas. Ability to assess and determine study requirement from protocol review
Strong Project and Risk Management
Understanding of regulatory requirements and relevant data standards
Strong communication, decision-making, influencing, negotiation, and project management skills
Technical skill and experience using relational databases and data visualization tools, e.g. Spotfire, JReview

Job Responsibility

Define and drive global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to deliver high quality clinical data
Plan and execute communication plans & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a project
Develop charters, resource utilization and project plans to achieve CDS specific goals
Develop people, including recruitment, retention, and career development and performance management
Able to resolve conflicts, influence and communicate cross-functionally with key stakeholders and customers
Provides administrative and central monitoring technical and process oversight of teams
Implements organizational design and develop succession planning for RBM in collaboration with other functional leaders
Oversee all technical aspects required to set up and test study level Risk-based Monitoring system
Anticipates, oversees and influences change to position efficient, high-quality implementation of required data flows to incorporate internal and external data sources into Pfizer informatics environment ensuring operational delivery and traceability from source. Ensures appropriate process and documentation are in place to support inspection readiness
Act as the key scientific and technical central monitoring expert

Fulltime

Clinical Trial Manager/ Sr Clinical Trial Manager (PM/ Sr PM)

Clinical Operations Lead - Early Development Oncology. ICON plc is a world-leadi...

Location

United States , Raleigh, Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

BS/BA degree or a relevant degree with strong emphasis on science, or equivalent experience
Minimum of five years of relevant experience in the biopharmaceutical industry or other relevant clinical research experience, with a focus on skills and competencies
Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health
Prior experience in assisting the conduct and management of multinational clinical trials is preferred
Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously
Experience in oncology studies required (phase I preferred)

Job Responsibility

Participate as a member of a working group and perform special projects, as assigned, to improve the efficiency, effective and quality of the functioning of the Development Operations department
Act as preliminary liaison for study sites to convey study information, answer questions and in accordance with the escalation pathway
Develop relationships with investigational sites, HCPs, and institutions to enhance conduct of the trial
Monitor study-specific timelines and key deliverables
focus on management of all relevant external vendors (e.g., Monitoring, Sample management, IVRS, Laboratory, etc)
Participate as a member of the multi-disciplinary trial(s) team
Participate in coordinating efforts with internal Pharmacovigilance, and safety group as needed
Participate in data review and discrepancy resolution as needed
Assist in the development of the IP and co-medication strategy (quantities, labels, depots, tracking, etc.) working closely with other departments
Plan and organize meetings with team support (e.g., investigator/coordinator meetings, DMC, SMC, safety call, etc.) as appropriate

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

Clinical Data Manager II/III

Location

Poland

Salary:

Not provided

GRUPA NEUCA

Expiration Date

Until further notice

Requirements

university degree (bioengineering, life science or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution
fluency in English
minimum 2 years of experience in effective clinical data management practices
excellent knowledge of MS Excel
ability to analyze information and draw conclusions, initiate appropriate solutions
independence in planning activities, resources and time to achieve the set goals and objectives
communication skills, teamwork and ability to contact with the client in order to learn about and solve problems

Job Responsibility

taking the role of Lead Data Manager for allocated projects
accountability for all DM deliverables per the established timeline
providing instruction to DM study team and reviewing their study team's output while adjusting
resource allocations within the project accordingly
overseeing all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCP
working with the Project Manager to build timelines to meet contracted milestones by communicating with leads in different disciplines and the project team
maintaining awareness of other Biometrics functional group deliverables to be able to support risk and mitigation strategies
ensuring service and quality agreed upon specifications per the DMP and scope of work
performing quality control in all aspects of the study
reconciling the clinical database against safety data, laboratory data or any other third party data as appropriate. Utilising local laboratory systems and batch data load facilities where appropriate

What we offer

work in a developing CRO in Poland with foreign branches
recommending appropriate solutions in projects
impact on changes in processes in the Data Management area
stable employment in the company awarded Top Employer 2026
work in an international team
remote work
private medical care
free legal advice
social benefits
employee referral program

Clinical Data Manager

Amaris is looking for a Clinical Data Manager with strong experience in clinical...

Location

Barcelona, Lyon, Paris, Madrid

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Experience in clinical data management for CROs (5–10 years)
Proficiency with industry-standard data management tools and software
Academic background in Life Sciences, Pharmacy, or related field
English fluent
You demonstrate strong analytical and problem-solving skills
You demonstrate excellent communication skills

Job Responsibility

Act as the main point of contact for all data management topics and participate in project/study meetings
Contribute to the selection of subcontractors by preparing specifications and evaluating proposals
Participate in study design, including data management sections in protocols and CRF specifications
Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality
Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions
Test eCRF before production deployment and after each protocol amendment
Implement targeted quality control of data based on risk assessment
Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.)
Approve SDTM specifications and verify SDTM packages as needed
Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures

What we offer

An international community bringing together 110+ different nationalities
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
A robust training system with our internal Academy and 250+ available modules
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
Opportunity to turn your ideas into action and make a tangible impact
Empowered to design and lead projects that create real social or environmental impact, with the company’s full support

Fulltime

Program Manager, Clinical Data Science, Sponsor Dedicated

We are currently seeking a Program Manager, Clinical Data Science to join our di...

Location

United States

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in data science, statistics, clinical research, or a related field
Extensive experience in program management within the clinical data science or related domain
Strong background in data science methodologies, statistical analysis, and clinical research, with a track record of successfully managing complex data-driven projects
Exceptional leadership skills with experience managing cross-functional teams and collaborating with various departments to achieve program objectives
Proficiency in project management tools and techniques, with experience in risk management, budgeting, and resource planning
Excellent communication and interpersonal skills, with the ability to convey complex data insights clearly and build effective relationships with stakeholders at all levels

Job Responsibility

Managing the end-to-end execution of clinical data science programs, including planning, resource allocation, and delivery of data science projects within scope, time, and budget constraints
Coordinating with data scientists, statisticians, clinical researchers, and other stakeholders to ensure alignment on project objectives, data requirements, and analytical approaches
Developing and maintaining program plans, timelines, and budgets, and monitoring progress to ensure timely and successful completion of data science initiatives
Providing strategic oversight and guidance on data science methodologies, ensuring that analyses are rigorous, valid, and aligned with clinical and regulatory standards
Communicating program status, insights, and outcomes to stakeholders, including executive leadership, and addressing any issues or risks that may impact program success

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

Manager, Clinical Data Management

The Manager – Clinical Data Management (CDM) is a senior functional expert in Cl...

Location

Italy , Milano

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Minimum of 7 years of experience in Clinical Data Management within pharma, biotech, CRO, or academic settings
Bachelor’s degree in life sciences, health informatics, pharmacy, computer science, or a related field
Strong understanding of clinical trial processes and data management principles
Experience with EDC systems (e.g., Medidata Rave, Veeva EDC)
Expertise in eCOA and RTSM systems
Familiarity with data visualization tools
Proficiency in statistical software (e.g., SAS)
Knowledge of regulatory requirements and CDISC standards
Strong organizational and communication skills
High attention to detail

Job Responsibility

Providing data management expertise during protocol development and amendments
Contributing to the selection of CROs and specialized vendors for data collection and management
Supporting the preparation and review of RFPs related to data management services and costs
Acting as the primary point of contact for CROs and vendors, ensuring high-quality deliverables within agreed timelines and budget
Ensuring compliance with company processes, ICH E6 guidelines, and applicable regulations
Collaborating on study timelines from start-up through close-out
Supporting the development, review, and testing of data collection tools (e.g., eCRFs, eCOA systems)
Contributing to the creation and maintenance of data management documentation (e.g., DMPs, Edit Check Specifications, Data Validation Plans)
Overseeing outsourced data management activities, including data cleaning, coding, and reconciliation
Maintaining oversight documentation and coordinating internal data quality reviews

What we offer

Competitive salary
Comprehensive benefits
Extensive opportunities for professional growth and development

Associate Director, Clinical Data Manager

Associate Director, Clinical Data Manager (Sponsor Dedicated). ICON plc is a wor...

Location

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Advanced degree in Data Science, Statistics, Bioinformatics, or a related field
Experience in all aspects of Data Management related clinical study planning and execution, and in executing the complete range of clinical study activities, from concept sheet through final study report and archiving
Proven experience as Clinical Data Manager in the pharmaceutical/biotechnology industry, equivalent to at least 10 years
Substantial project management experience
Strong leadership competencies and influencing skills
Effective oral and written communication skills
Proven team dynamic knowledge and skills and ability to foster partnerships across projects and multidisciplinary teams
Growing expertise in drug development, including some knowledge of interfaces and interdependencies of clinical development with other functions (e.g., nonclinical & pharmaceutical development, regulatory, commercial/marketing)
Successful completion of multiple studies from beginning to end providing a full scope of DM experience

Job Responsibility

Leading Data Management including centralized monitoring related activities within a complete clinical development program (Phase I-IV, Accountable and Project Leadership) for global or regional trials and/or programs with different complexity
Serving as the escalation point, work with CRO data managers, vendors, internal team members for resolution
Ensures and tracks data quality of clinical database/deliverables (incl. CRF and non-CRF data) and submission readiness of the clinical data management deliverables and data packages (e.g. CDISC)
Project management of all clinical data management related deliverables including operationalization by steering internal and external experts and specialist. Ensuring adherence to planned time, cost and quality
Execution of the clinical data collection strategy in accordance to Sponsor Standards
Accountable for oversight of CROs in the execution of Phase I – IV clinical trial(s)
Represents Data Management within the Global Trial Team and serves as the key Global Development Operations point of contact for the DM related tasks in a trial/project/program
Key contributor to the development of reports and communicating to relevant line management and Clinical Operations Teams
Drives, leads and manages the successful execution, oversight and approval of all DM related clinical trial documents and operational plans (e.g. Data Management Plan) of clinical trials using strong project management, leadership, and organizational skills
Ensures strong oversight, review and delivery of trial/project DM related CAPAs in order to meet corporate compliance standards and timelines

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

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Data Manager, Clinical Data Sciences

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