JUMP TO CONTENT
Shortlist
search jobs Search
About the role ICON and you Application Process Day in the life Who we are

Clinical Data Delivery Lead ll

010862_2

About the role

This vacancy has now expired. Please click here to view live vacancies.
Clinical Data Delivery Lead II
 
Competitive Package
 
This is an exciting opportunity toworkwithin a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The Clinical Data Delivery Lead III is responsible for overseeing the set-up and maintenance of clinical data deliverables on multiple clinical studies. The Clinical Data Delivery Lead III participates in activities as related to the specification, validation and quality assurance of study data deliverables and applies good experience and knowledge in support of the clinical data programmers assigned to a clinical study.
 
Overview of the Role
  • Serves as the clinical data delivery lead on study specific programming setup, leading clinical data programming activities on multiple studies of simple to moderately complex design, with good clinical data delivery experience and knowledge.
  • Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
  •  Reviews specification documents created by study teams, such as data transformation specifications and programming specifications.
  • Quality assures programming outputs and support validation activities per the formal, documented QC process.
  • Plans and works with the clinical programming group to schedule specification, programming and validation activities. Manages timelines for programming setup process, ensures issues are addressed in a timely manner to meet timelines and produces clinical data delivery validation packages for delivery to the study teams to file in the Trial Master File.
  • Co-ordinates study database updates as specified per Change Request documents and procedures. Performs an Impact Analysis and Risk Assessment of the proposed changes.
  • Serves on project teams to coordinate and lead development activities for clinical data programming projects.
  • Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive criticism.
  • Keeps those responsible for project management informed of any issues that might impact project target dates, scope or budget and escalates potential problems effectively and in a timely manner.
  • Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.
  • Trouble-shoots and solves study data delivery issues and/or external data integration issues and/or change request issues using the appropriate applications.
  • Ensures high quality deliverables by providing senior review of study-level/program-level/multi-study core deliveries for accuracy.
  • Attends sponsor audits and assists with in-progress audits, including presenting the Clinical Data Delivery process and procedures and pretending the validation documentation produced by the Clinical Data Service Group.
  • To participate and contribute towards internal user group meetings to share knowledge and providing latest updates/features. Participates in Data Management department initiatives.
  • Plan for the study clinical data delivery in detail thereby providing clarity on all aspects of the setup progress.
  • Maintaining all necessary study documentation for the clinical data delivery.
  • Ensures all clinical data delivery queries are responded to in a timely manner. Ensures that queries that cannot be resolved are routed to the correct SME and the issue is perused until resolved.
  • Contributes to training materials on a process, system or technology level. Works with CTD and Clinical Data Services Management on delivery of training courses, instructor-led and on-the-job
 
Role Requirements / Skills / Experience Required
  • Minimum 4 years relevant clinical research data delivery experience.
  • Proven clinical research data delivery experience.
  • Demonstrated ability to produce CDISC and Sponsor defined clinical data deliverables
  • Experience with clinical data programming and the ability to review and evaluate clinical data.
  • Extensive problem solving skills for tasks/functions related to his/her group.
  • Strong organizational, prioritization and time management skills as to effectively organize workload and complete assignments.
  • Ability to successfully manage multiple tasks and timelines.
  • Ability to perform assigned tasks with little supervision.
  • Ability to liaise professionally with team members.
  • Team player with strong verbal and written communication skills.
  • Demonstrated ability to learn new technologies, applications and techniques.
Benefits of Working in ICON
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
 
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   
 
What’s Next?
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 

*LI-AR2

List #1

Day in the life

Headshot of female
Building a Career at ICON: Susie's journey from HR Analyst to Senior VP

Teaser label

Inside ICON

Content type

Blogs

Publish date

08/07/2025

Summary

Building a Career at ICON: A Conversation with Susie McEvoy, Senior VP of HR At ICON, career journeys are rarely linear – and Susie McEvoy’s story is a powerful example of that. From joining as a

Teaser label

Discover how Susie built a successful career at ICON, progressing from HR Analyst to Senior Vice President.

Read more
Nurse
Career Guide: Clinical Research Nursing

Teaser label

Inside ICON

Content type

Blogs

Publish date

08/01/2025

Summary

Clinical Research Nursing: A Vital Career at ICON Clinical research nursing is a specialised discipline that blends expert patient care with the science of clinical trials. Nurses in this role ar

Teaser label

Learn about key responsibilities and how to start your career in clinical research nursing.

Read more
stethoscope on paper records
Clinical Trial Management Systems (CTMS) Demystified

Teaser label

Inside ICON

Content type

Blogs

Publish date

07/28/2025

Summary

CTMS: The Essential Tool for Clinical Research Professionals Clinical trials have rapidly evolved, accelerated by technology and digital innovation. Central to this evolution is the Clinical Tria

Teaser label

Explore the Clinical Trial Management System (CTMS), its core functions, market growth, and career advantages.

Read more
View all

Similar jobs at ICON

Software Engineer

Salary

Location

US, New York, NY, Rochester

Department

Full Service - Development & Commercialisation Solutions

Location

Rochester

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Software Engineer

Job Type

Permanent

Description

We are currently seeking a Software Engineer to join our diverse and dynamic team. As a Software Engineer at ICON, you will play a crucial role in developing and implementing software solutions that e

Reference

JR132906

Expiry date

01/01/0001

Kris Costello

Author

Kris Costello
Kris Costello

Author

Kris Costello
Read more Shortlist Save this role
Read more Shortlist Save this role
Manager, Project Management

Salary

Location

US, New York, NY, Whitesboro

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Whitesboro

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Project/ Program Management

Job Type

Permanent

Description

We are currently seeking a Manager of Project Management at ICON Plc to join our diverse and dynamic team. As the Manager of Project Management, you will be responsible for the overall direction and m

Reference

JR133105

Expiry date

01/01/0001

Hanna Pitcairn

Author

Hanna Pitcairn
Hanna Pitcairn

Author

Hanna Pitcairn
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

Denmark

Department

Clinical Monitoring

Location

Denmark

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA in Denmark you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.

Reference

2025-121593

Expiry date

01/01/0001

Alison Burton

Author

Alison Burton
Alison Burton

Author

Alison Burton
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

Sweden

Department

Clinical Monitoring

Location

Sweden

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA in Sweden you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.

Reference

2025-121592

Expiry date

01/01/0001

Alison Burton

Author

Alison Burton
Alison Burton

Author

Alison Burton
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

Finland

Department

Clinical Monitoring

Location

Finland

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA in Finland you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.

Reference

2025-121594

Expiry date

01/01/0001

Alison Burton

Author

Alison Burton
Alison Burton

Author

Alison Burton
Read more Shortlist Save this role
Read more Shortlist Save this role
Systems Analyst

Salary

Location

US, Lenexa KCIB (PRA)

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Analyst

Job Type

Permanent

Description

Overview:At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. O

Reference

JR132931

Expiry date

01/01/0001

Hanna Pitcairn

Author

Hanna Pitcairn
Hanna Pitcairn

Author

Hanna Pitcairn
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above