Senior CDC job in

This vacancy has now expired. Please click here to view live vacancies.

At ICON, it's our People that set us Apart

Are you passionate about improving the quality of human life? If so, we invite you to join us in creating a healthier world tomorrow.

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I-IV clinical studies.

We started as a team of 5 members in 1990 & today we are ranking at top 4 worldwide based on revenue of 2015. Currently we have 12200+ employees across the globe. ICON is a $1.575bn company having its presence across 89 offices in 37 countries.

Job Title : Sr Clinical Data Coordinator

Reporting to : Manager

Type of Employment : Full Time

Location : Chennai / Trivandrum

No of yrs. of exp : 6+ relevant yrs. Of experience

Summary:

In accordance with project specific timelines, to perform data management activities to ensure the generation of accurate, complete, and consistent clinical databases.

To assist with the training of less experienced Clinical Data Coordinators.

To fulfill his / her job responsibilities in accordance with Good Clinical Practices (GCPs), ICON Standard Operating Procedures (SOPs), Working Procedures (WPs),Study Specific Procedures (SSPs), International Committee on Harmonization (ICH) Guidelines, and all applicable laws and regulations.

Key Responsibilities & Duties:

Complete all assigned trainings (including the Study Lead Development program) and co rses in the ICON Training Management system (iLearn); ensuring that mandatory courses are all completed before the designated date and that the required system specific training has been completed for current studies.

Record all billable and non-billable time in the appropriate timesheet management system (e.g. PlanviewTM).

Review CRF / eCRF data for completeness, accuracy, and consistency via computerized edits and manual data checks.

Perform external data reconciliation.

Perform Serious Adverse Event reconciliation.

Generate and close/resolve (as appropriate) data queries.

Freeze and/or lock eCRFs (as appropriate) within the Electronic Data Capture System.

Create and maintain study files and other appropriate study documentation.

Perform User Acceptance Testing and collaboratively work with CDMS personnel to see issues found through re-testing and resolution.

Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.

Train and guide less experienced CDCs in data management requirements and activities.

Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).

As required, communicate effectively with the Project team, Study Lead, Project Lead and Project Manager.

Experience required

A minimum of 6 year relevant clinical research industry experience.

Prior relevant clinical research industry experience.

Excellent written and oral communication skills.

Excellent accuracy and attentiveness to detail.

Capability to work within a team environment.

Academic or Trade qualifications: Any graduate

Benefit Working with ICON:

Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, and life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

PROCESS

Technical and competency selection:

When you spot an opportunity youre interested in and submit an application, one of our Talent Acquisition Specialists will contact you to evaluate your suitability for this position, as well as for other openings within the business.

The evaluation will look at your technical skills and your competencies for example, delivering excellence.

Interview

After this, well let you know if well be progressing with your application. If you have been successful at this stage, we will talk you through a telephone interview. This will then be followed by an interview with our Hiring Manager, either face to face or by tele-conference.

Offer

If youre successful, we will notify you with details of the offer, talk you through our culture and values, answer any questions you may have and above all, welcome you to the ICON team.

Impactful work. Meaningful careers. Quality rewards.

At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential.
Learn more about Our Culture at ICON

List #1

Day in the life

Building Careers Across Latin America

Teaser label

Our People

Content type

Blogs

Publish date

06/04/2026

Summary

After more than 20 years at ICON, Carolina Boari has witnessed the organisation's growth across Latin America while building a successful career of her own. Today, as Executive Director of Clini

Teaser label

Sajna's Biometrics Career Journey

Teaser label

Our People

Content type

Blogs

Publish date

05/26/2026

Summary

From Data Management to Leadership For Sajna Basant, a career in Biometrics has always been about more than data. “Data is not just numbers,” she explains. “It represents real people, their health

Teaser label

Discover how Sajna built her career in Biometrics at ICON.

Image of pencil on paper, charts drawing, and laptop

How Clinical Project Managers Keep Complex Trials Moving Forward

Teaser label

Industry

Content type

Blogs

Publish date

05/18/2026

Summary

How Clinical Project Managers Keep Complex Trials Moving Forward linical trials are becoming more complex than ever. Global study footprints, evolving regulations, increasing data demands, and tigh

Teaser label

Learn what it takes to succeed in Clinical Project Management in modern clinical research.

View all

Similar jobs at ICON

Site Services Specialist I

Salary

Location

India, Bangalore

Department

Full Service - Development & Commercialisation Solutions

Full Service - Global Business Services

Location

Bangalore

Bengaluru

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Research In-Home Services

Job Type

Permanent

Description

Job Advert PostingAs a Site Services Specialist I at ICON, you will support clinical trial sites by managing logistics, resolving site-related issues, and ensure that sites are equipped with the neces

Reference

JR152412

Expiry date

01/01/0001

Author

Puja Jaiswal

Author

Puja Jaiswal

Read more Shortlist Save this role

Contract Analyst I

Salary

Location

India, Bangalore

Department

Full Service - Corporate Support

Location

Bangalore

Bengaluru

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Corporate Support

Job Type

Permanent

Description

We are seeking a Contract Analyst I to join our diverse and dynamic Client Contract Services (CCS) Team at ICON. In this role, you will play a key part in managing the budgeting and drafting of Contra

Reference

JR153255

Expiry date

01/01/0001

Author

Puja Jaiswal

Author

Puja Jaiswal

Read more Shortlist Save this role

Site Management Associate I

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Hybrid

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of opera

Reference

JR152750

Expiry date

01/01/0001

Author

Elizabeth Davies

Author

Elizabeth Davies

Read more Shortlist Save this role

Manager, Statistical Programming

Salary

Location

India, Bangalore

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Hybrid

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Programming

Job Type

Permanent

Description

As a Manager, Statistical Programming at ICON, you will lead a team of statistical programmers in the development and validation of statistical analysis and reporting solutions for clinical trials.Wha

Reference

JR148419

Expiry date

01/01/0001

Author

Chethana Nelliadka Kamalaksha

Author

Chethana Nelliadka Kamalaksha

Read more Shortlist Save this role

Senior CRA

Salary

Location

Philippines, Manila

Location

Manila

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (SCRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinica

Reference

JR146422

Expiry date

01/01/0001

Author

Maria Clare

Author

Maria Clare

Read more Shortlist Save this role

Clinical Associate - CTA

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Operations

Job Type

Permanent

Description

As a CTA at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.What You Will Do:You will contr

Reference

JR153072

Expiry date

01/01/0001

Author

Brandon Pupek

Author

Brandon Pupek

Read more Shortlist Save this role

About Icon

Overview of Service Lines

Full Service

ICON Strategic Solutions

Global Business Services

Global Office Locator

Inclusion & Belonging

ICON Cares - ESG

Building a Successful Clinical Research Resume

Landing Your First Job in Clinical Research

graduate What does full service mean for you?

Senior CDC

About the role

This vacancy has now expired. Please click here to view live vacancies.

At ICON, it's our People that set us Apart

ICON and you

About ICON

Career Pathways

Benefits & Rewards

Inclusion & Belonging

Environmental, Social & Governance

Global Office Locator

Impactful work. Meaningful careers. Quality rewards.