JUMP TO CONTENT
Shortlist
search jobs Search

Senior CDC

052590_2
052590_2

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


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.
List #1

Day in the life

Ovarian cancer knot being held in woman's hands
Standing Strong on Ovarian Cancer Day

Teaser label

Inside ICON

Content type

Blogs

Publish date

05/08/2025

Summary

Standing Strong on Ovarian Cancer Day:    ICON's Commitment to Advancing Care Ovarian cancer remains one of the most challenging gynaecologic malignancies, both in terms of detection and treatmen

Teaser label

Martin Lachs, VP, Oncology Project Management at ICON discusses ICON’s role in advancing ovarian cancer research.

Read more
Nurse and patient
Patient Centricity in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

05/07/2025

Summary

Patient Centricity in Clinical Research: What it is and Why it Matters In the past, clinical research was designed around the needs of sponsors, researchers, and regulatory bodies. Patients were of

Teaser label

Discover how patient centricity is reshaping clinical research by placing participants at the heart of study design and execution.

Read more
Liquid capsules
Navigating Regulatory Landscapes - FDA, EMA, & MHRA

Teaser label

Industry

Content type

Blogs

Publish date

05/05/2025

Summary

Navigating Regulatory Landscapes:     Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro

Teaser label

Compare FDA, EMA, and MHRA regulatory frameworks for clinical trials, and why this knowledge matters.

Read more
View all

Similar jobs at ICON

Site Activation Partner I

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Study Start Up Associate you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions. You will be d

Reference

2025-119209

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Read more Shortlist Save this role
CRA II - Toronto

Salary

Location

Toronto

Department

Clinical Monitoring

Location

Toronto

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. En tant qu’ARC (Associé(e) de recherche clinique), vous rejoin

Reference

2025-119397

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
Read more Shortlist Save this role
CRA II

Salary

Location

US, Blue Bell (ICON)

Department

Clinical Monitoring

Real World Solutions

Location

Portland

San Antonio

Raleigh

Blue Bell

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a CRA II to join our diverse and dynamic team. As a CRA II at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are c

Reference

JR130668

Expiry date

01/01/0001

Jasmine Garcia

Author

Jasmine Garcia
Jasmine Garcia

Author

Jasmine Garcia
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

US, Blue Bell (ICON)

Department

Clinical Monitoring

Real World Solutions

Location

Portland

San Antonio

Raleigh

Blue Bell

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

JR130667

Expiry date

01/01/0001

Jasmine Garcia

Author

Jasmine Garcia
Jasmine Garcia

Author

Jasmine Garcia
Read more Shortlist Save this role
Read more Shortlist Save this role
Clinical Research Associate (Field-Based) - Cross TA/Oncology - Toronto

Salary

Location

Toronto

Department

Clinical Monitoring

Location

Toronto

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. En tant qu’ARC (Associé(e) de recherche clinique), vous rejoin

Reference

2025-118864

Expiry date

01/01/0001

Monica Hawkins

Author

Monica Hawkins
Monica Hawkins

Author

Monica Hawkins
Read more Shortlist Save this role
Read more Shortlist Save this role
Clinical Research Nurse I (PRN)

Salary

Location

US, Lenexa KCI (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Nurse

Job Type

Temporary Employee

Description

We are currently seeking a Clinical Research Nurse I to join our diverse and dynamic team. As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical

Reference

JR125862

Expiry date

01/01/0001

Muna Nelke

Author

Muna Nelke
Muna Nelke

Author

Muna Nelke
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above