Clinical Lead for Data and Digital Job at Royal College of General Practitioners (London)

Associate Vice President, Clinical Data Management

The Associate Vice President, Clinical Data Management is a member of the Global...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s or master’s degree with 25+ years of data management experience
10 to 15 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
Experience within clinical data management, regulatory compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment
Expertise in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM)
Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen’s global clinical development efforts
Expertise in AI/ML-driven data management solutions, automation, and advanced analytics
Understanding of clinical data standards (CDISC, SDTM, ADaM)
Experience leading regulatory submissions, including NDA/BLA/MAA filings and advisory committee interactions
Proven ability to drive organizational change, optimize processes, and implement lean principles in clinical data management
Cross-functional collaboration experience with clinical operations, regulatory affairs, biostatistics, and R&D teams

Job Responsibility

Develop and drive the global data management strategy in alignment with clinical development objectives and corporate goals
Provide strategic and operational leadership to the Clinical Data Management (CDM) function across all clinical programs and phases
Lead innovation initiatives, including the implementation of development integration programs and the adoption of cutting-edge technologies to enhance data workflows
Represent Clinical Data Management in executive leadership discussions, regulatory interactions, and industry forums
Establish and enforce robust clinical data governance models, policies, and risk mitigation strategies to ensure quality and compliance
Make final decisions regarding standard operating procedures (SOPs), CDM best practices, and process optimization
Engage key stakeholders and ensure timely resolution on critical data integrity and regulatory compliance issues
Serve as the primary CDM representative during regulatory inspections and audits, with responsibility for final decisions on findings, responses, and corrective actions
Influence cross-functional clinical development, operational, and regulatory strategies through data-driven insights and analytics
Partner closely with Clinical Program Operations, Regulatory, Biostatistics, and R&D to ensure seamless integration and alignment of clinical data

Product Marketing Senior Lead

At WHOOP, we're on a mission to unlock human performance and healthspan. WHOOP e...

Location

United States , Boston

Salary:

150000.00 - 190000.00 USD / Year

Whoop

Expiration Date

Until further notice

Requirements

7+ years of product marketing experience, ideally in consumer health technology, digital health, wellness, or healthcare services
Proven success launching and marketing clinically oriented or science-based products to consumer audiences
Strong command of go-to-market planning, positioning development, and performance measurement across marketing channels
Experience working with scientific or clinical teams to ensure content accuracy and regulatory alignment
Excellent communication and storytelling skills with ability to make the complex feel accessible and meaningful
Strong cross-functional collaboration skills with a track record of influencing without authority
Ability to thrive in fast-paced, ambiguous environments while maintaining strategic clarity and executional rigor
BS/BA required
life sciences, health sciences, marketing or related field preferred. MBA or advanced degree a plus
Strong commitment to embracing and leveraging AI tools in day-to-day tasks, ensuring AI-assisted work aligns with the same high-quality standards as personal contributions

Job Responsibility

Lead go-to-market strategy and execution for WHOOP Advanced Labs and future healthcare product expansions
Develop positioning and messaging frameworks that balance scientific accuracy with consumer accessibility
Create and execute integrated marketing plans, aligning across channels and optimizing for performance
Partner with Clinical, Product, and Medical Affairs teams to ensure marketing efforts reflect regulatory standards and scientific integrity
Translate member insights and clinical data into actionable marketing strategies that drive awareness, adoption, and engagement
Collaborate with Brand, Creative, and Lifecycle Marketing teams to build member education and communication strategies for healthcare offerings
Serve as the primary product marketing partner for healthcare product leadership, influencing roadmap prioritization and market strategy

What we offer

equity
benefits

Fulltime

New

Central Monitor - FSP

The Central Monitor (CM) plays a key role for Data Surveillance by overseeing an...

Location

Serbia

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

University degree in life science, business or operations
Fluent in both written and spoken English
≥ 5 years of recent pharmaceutical industry experience, with previous experience in clinical research, in a Pharmaceutical Industry or CROs
Strong clinical experience with excellent understanding of clinical trial development and risk management processes and the management of clinical trials
≥ 3 years comprehensive experience in monitoring (central, site), additional experience in clinical data analytics, data management activities or equivalent is preferable
Specific Central monitoring / monitoring experience (hands-on experience with KRIs review, centralized monitoring and quality tolerance limits -QTLs-) are strongly preferred
Knowledge of Risk-Based Quality Management (RBQM) and adaptive monitoring principles
Knowledge of overall clinical trial management process, understanding of the protocol, study associated risks and their significance, and the risk management process
Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards (GCP/ICH)
Critical thinking and analytical skills to understand/analyze complex data and provide insight into risk signaling, trends, and outliers in data

Job Responsibility

Implement and execute centralized monitoring strategies to support clinical trial oversight
Conduct ongoing central monitoring analysis of clinical trial data to detect trends and signals
Work with Data Analysts team in reviewing CM technology outputs and performing an initial investigation of identified risks (e.g., atypical data patterns) to assess their scope and nature in preparation for review with study teams
As needed, provide input into the data domains required for central monitoring as per the monitoring strategy
Ensure adherence to risk-based monitoring plans, SOPs, and industry best practices
Perform data surveillance via the CM platform, identifying potential sites or trial risks in alignment with the IQRMP
Collaborate with Lead CM and study teams to refine and implement risk-based monitoring plans
Provide insights and recommendations to enhance trial efficiency and mitigate risks
Support root cause analysis for identified issues and suggest corrective actions
Generate and summarize findings within the CM platform and lead the communication of results to study teams and RSL

New

Central Monitor - FSP

The Central Monitor (CM) plays a key role for Data Surveillance by overseeing an...

Location

Romania

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

University degree in life science, business or operations
Fluent in both written and spoken English
≥ 5 years of recent pharmaceutical industry experience, with previous experience in clinical research, in a Pharmaceutical Industry or CROs
≥ 3 years comprehensive experience in monitoring (central, site), additional experience in clinical data analytics, data management activities or equivalent is preferable
Specific Central monitoring / monitoring experience (hands-on experience with KRIs review, centralized monitoring and quality tolerance limits -QTLs-) are strongly preferred
Knowledge of Risk-Based Quality Management (RBQM) and adaptive monitoring principles
Knowledge of overall clinical trial management process, understanding of the protocol, study associated risks and their significance, and the risk management process
Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards (GCP/ICH)
Critical thinking and analytical skills to understand/analyze complex data and provide insight into risk signaling, trends, and outliers in data
Strong analytical and critical thinking skills with the ability to interpret complex clinical and operational data, recognize patterns, and identify potential risk signals or issues

Job Responsibility

Implement and execute centralized monitoring strategies to support clinical trial oversight
Conduct ongoing central monitoring analysis of clinical trial data to detect trends and signals
Work with Data Analysts team in reviewing CM technology outputs and performing an initial investigation of identified risks
As needed, provide input into the data domains required for central monitoring as per the monitoring strategy
Ensure adherence to risk-based monitoring plans, SOPs, and industry best practices
Perform data surveillance via the CM platform, identifying potential sites or trial risks in alignment with the IQRMP
Collaborate with Lead CM and study teams to refine and implement risk-based monitoring plans
Provide insights and recommendations to enhance trial efficiency and mitigate risks
Support root cause analysis for identified issues and suggest corrective actions
Generate and summarize findings within the CM platform and lead the communication of results to study teams and RSL

Senior Manager Global Category-Digital Health and Regulated Tech

We are seeking an individual who thrives in ambiguity, capable of driving catego...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Familiarity with procurement platforms such as Ariba, as well as ERP systems and advanced analytics tools
Excellent problem solving and organizational skills
Strong analytical skills, including the ability to analyze large datasets, identify trends, and derive actionable insights
Experience leading large, cross-functional teams and managing complex global projects in a matrixed environment
Strong knowledge of regulated software and digital health procurement
Familiarity with compliance frameworks (21 CFR Part 11, GxP, HIPAA, GDPR)
Experience with vendors in clinical technology, digital health, and connected medical solutions
Doctorate degree and 5 years of Global Strategic Sourcing, Procurement experience
Or Master’s degree and 12 years of Global Strategic Sourcing, Procurement experience
Or Bachelor’s degree and 15 years of Global Strategic Sourcing, Procurement experience

Job Responsibility

Lead category management for Digital Health and regulated technology software supporting clinical trials, patient engagement, and regulated applications
Partner with R&D, Clinical, Regulatory, and Compliance teams to ensure alignment with FDA, EMA, HIPAA, and GDPR standards
Negotiate contracts with vendors of e-clinical, ePRO, EDC, and patient-facing apps, balancing innovation with compliance
Build governance frameworks ensuring cybersecurity, data privacy, and quality system compliance for regulated digital solutions
Monitor evolving digital health regulations and integrate compliance into sourcing strategies
Provide strategic oversight as the lead for Digital Health and Regulated Software category and sourcing
Act as a trusted advisor to ensure that procurement initiatives are aligned with broader organizational objectives
Guide and facilitate collaboration across cross-functional teams and regional stakeholders
Ensure that all Software procurement activities are managed in compliance with regulatory, contractual, and operational risk requirements
Collaborate with Strategic Sourcing peers to oversee the strategic approach to complex negotiations for Software contracts

Lead Data Engineer

The Data Provisioning solution enables the ingestion of non-CRF data into our cl...

Location

Poland , Warsaw

Salary:

Not provided

Astek

Expiration Date

Until further notice

Requirements

Strong understanding of technical aspects of digital device data
Experience with big data ingestion, processing, and storage
Ability to analyze data and interpret technical information effectively
Proficient in technologies such as AWS, Python, Snowflake, Airflow, Amazon EMR, and Spark (e.g., PySpark)
Familiar with Tableau, Terraform, and CI/CD principles and tools
Demonstrate thought leadership and excellent communication skills
Experience with validated projects and working with clinical trial data, ideally including DHT (Digital Health Technology) data and related processes

Job Responsibility

Lead, coach, and mentor the development/technical team, ensuring best practices and coding standards are followed
Coordinate technical resources and communicate relevant changes in infrastructure, systems, or processes within the organization
Design technical solutions and review designs proposed by the team
Provide technical support and guidance to study teams, including troubleshooting data issues
Conduct code reviews and ensure compliance with GxP requirements
Maintain and improve quality of technical documentation and user stories in Jira
Understand current systems and interfaces, contribute to platform planning, and help define the technical roadmap
Collaborate with Product, Project, and Validation teams to optimize technical resources and ensure effective testing and validation
Optionally, take on the System Owner role as needed

What we offer

Experience accelerator, where every assignment is an opportunity to progress
Access to a multitude of technically exciting projects for our clients as well as internally
Individualized, local support for a tailored career path
Continuous learning, thanks to our internal training academy
A friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practices

Veeva Clinical Digital Systems Analyst

Parexel is currently seeking a Veeva Clinical Digital Systems Analyst to join us...

Location

Poland

Salary:

260000.00 - 351000.00 PLN / Year

Parexel

Expiration Date

Until further notice

Requirements

Bachelor’s degree, science, healthcare and/or technology preferred
At least 5 years of experience in clinical related technology for the pharmaceutical/biotechnology industry
IT-literate and passionate/experienced towards new technology and digital systems (e.g. Microsoft-based applications, LMS, CTMS, eTMF, clinically focused subscription databases)
An experienced clinical trials professional who is well versed in the field of clinical study management activities, combined with excellent project management, training & mentoring capabilities
Extensive pharmaceutical or related industry experience
Substantial previous clinical trials experience, with emphasis on GxP and compliance
Has a sound working knowledge of clinical operations, clinical processes, medical terminology, global CROs and vendor management
Knowledge of FDA/ICH guidelines and industry standard practices regarding the management of clinical trial data and studies
Working knowledge of FDA Guidance Documents: Computerized Systems Used in Clinical Trials, General Principles of Software Validation
Working knowledge of 21 C.F.R. Part 11

Job Responsibility

Represents their department and collaborates with Information Services (IS) regarding the implementation and management of digital systems/technology used
Facilitates the design, development, production and delivery of digital systems to achieve operational excellence, optimize data quality and realize efficiencies wherever possible
Accountable for the delivery of digital systems, working alongside IS counterparts and other departments
Acts as a key point of contact between on any new digital systems, and as an expert advisor to the other business departments in these matters
Works with the ‘Performance and Training’ function to facilitate the collation, visualization, analysis & storage of relevant metrics to ensure optimal trial performance and aid continuous improvement
Organizes and delivers relevant specialist training sessions and workshops with a key focus on digital systems
Identifies new technologies that may be relevant, assists with building business cases, ROI, etc. to support need for implementation
Ensures global consistency of approach for digital systems and technologies between clinical trials by increasing awareness of those systems/technologies
Establishes, maintains, reviews and manages the digital systems (e.g. CTMS, other ‘platform’ systems)
Lead on CTMS, eTMF, and other Clinical Systems management

What we offer

participation in Parexel’s annual performance-based bonus plan
annual salary review
total rewards incentives
open and friendly work environment
opportunities to develop long-term careers
develop within your role and tackle further responsibilities or develop your skill set within other related departments

Fulltime

Lead Healthcare Data Analyst

As a Lead Data Analyst, you will provide leadership to analysts building and imp...

Location

United States , Miami

Salary:

115444.27 - 150077.55 USD / Year

Baptist Health

Expiration Date

Until further notice

Requirements

Masters or PhD Degree in a quantitative field (mathematics, computer science, physics, economics, engineering, statistics, operations research, etc.)
Minimum of 10 years of experience
Must have healthcare data analyst experience
Proven working experience as a Lead data analyst
Experience in leading teams that work on data querying, visualization, dashboarding and/or scorecard tools
Expert level skills in SQL, Excel, Tableau or similar
Ability to apply data visualization, descriptive and summary statistical techniques for discovery and timely insights (data exploration, ad-hoc queries, and analysis)
Hands on experience with statistical analysis, visualization, and data mining tools such as R and Python
Strong Power BI experience required
DBT Cloud experience required

Job Responsibility

Provide leadership to analysts building and implementing advanced analytics solutions that drive valuable insights and create actionable health and wellness solutions
Define analytics strategies that supports business objectives through data mining & identifying opportunities to improve current processes or identifying new ways to achieve desired benefits
Design methods of exploratory analysis & derive insights through the collection, aggregation, and assessment of data from a variety of internal and external sources including digital and clinical exhaust/telemetry data
Guide others to identify correlations and causations across data sets
Presents findings and recommendations in simple and clear ways to drive action
Monitor production report, dashboard and other analytics processes to ensure proper service recovery

Fulltime

Clinical Lead for Data and Digital

Royal College of General Practitioners

Location:
United Kingdom , London

Category:
Public Sector

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 05, 2026

Expiration:
April 07, 2026

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