JUMP TO CONTENT

DOCS Operations Manager

JR073413

About the role

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

Job Advert Posting

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.

Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

Responsibilities:

CPC MANAGEMENT

Complete DOCS induction and orientation for newly employed CPCs.

Ensure client-specific induction and orientation is planned, communicated and completed.

Establish goals and objectives for each CPC.

Monitor performance and conduct annual appraisal for each CPC, as applicable. Conduct regular 1:1 meetings with assigned CPCs.

Ensure timely submission and approval of time reports, expense reports and leave

requests for assigned CPCs.

Manage non-rechargeable expenses for assigned CPCs, per regional guidelines. Create a positive relationship between DOCS, the CPC and the client to ensure retention.

Conduct accompanied site visits, if applicable / approved. Ensure timely identification, resolution and escalation of issues.

Implement, monitor and ensure appropriate completion of a Corrective Action Plan, if required.

Monitor and update relevant CPC data in OMNI.

CLIENT RELATIONSHIP MANAGEMENT

Establish routine teleconference and meeting schedule with client contact(s) to effectively manage client relationship.

Obtain regular client feedback to ensure CPCs are meeting performance expectations and PDPs are aligned with client goals.

Agree Key Performance Indicators (KPIs) with client and periodically review results. Ensure compliance with time and expense reporting requirements of client contracts. Collaborate with client to forecast resource requirements.

Ensure DOCS understands current client procedures and expectations.

Proactively plan for contract extensions, completions and terminations in collaboration with client and relevant DOCS departments

DOCS BUSINESS PROCESS MANAGEMENT

Participate in Business Development activities, as appropriate. Contribute to process improvement initiatives, as requested. Up to 20% domestic and/or international travel, as needed. Other duties as assigned.

  • Experience Needed: At least 3-4 years operational experience in clinical trials with a pharmaceutical company and/or a CRO is required. Demonstrated knowledge of clinical development processes, global clinical operations, and strategic planning is required. Familiarity with industry best practices for vendor management is required. Good understanding of the therapeutic areas where Janssen is involved is preferred.

Experience with Digital Health technology suppliers, digital platforms and technologies is preferred. Strong IT skills in appropriate software and company systems. Demonstrate a passion for digital technologies and how these are implemented in clinical studies.

Strong project management skills and presentation skills with the ability to lead a team independently is required.

Excellent in speaking and writing in English. Effective communication skills, oral and written.

Education: BA degree required

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

List #1

Day in the life

Female portrait
A Career in Patient Safety: Karina's Journey at ICON

Teaser label

Our People

Content type

Blogs

Publish date

11/14/2025

Summary

Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a

Teaser label

Explore a pharmacovigilance career at ICON through Karina Espinoza's story.

Read more
Headshot of female
How Patient Impact Shapes Clinical Operations

Teaser label

Our People

Content type

Blogs

Publish date

11/13/2025

Summary

A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout

Teaser label

Victoria DeVeaugh Geiss shares insights from 20+ years in the industry and why patients remain at the heart of her work.

Read more
Two medics at ICON clinical research clinic
The Strategic Role of Site Selection and Activation in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

10/28/2025

Summary

Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit

Teaser label

Explore the critical role of site selection and activation in clinical trials.

Read more
View all

Similar jobs at ICON

(Senior) Clinical Research Associate

Salary

Location

Belgium, Mechelen

Location

Mechelen

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

📌 Job Opportunity: Clinical Site Manager / Senior CRA We are looking for an experienced clinical research professional who is passionate about partnering with study sites, safeguarding study quality,

Reference

JR138943

Expiry date

01/01/0001

Vanessa Verdickt Read more Shortlist Save this role
Manager, Regulatory Affairs

Salary

Location

Japan, Tokyo

Location

Osaka

Tokyo

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug / Device Regulatory Affairs

Job Type

Permanent

Description

We are currently seeking a Senior Manager, Regulatory Affairs to join our diverse and dynamic team. As a Senior Manager, Regulatory Affairs at ICON, you will play a pivotal role in designing and analy

Reference

JR137082

Expiry date

01/01/0001

Haruna Yamabayashi Read more Shortlist Save this role
Clinical Quality Project Manager

Salary

Location

Spain, Madrid

Location

Paris

Frankfurt

Warsaw

Barcelona

Madrid

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Project Management

Job Type

Permanent

Description

We are currently seeking a Clinical Quality Project Manager to join our diverse and dynamic team. As a Clinical Quality Project Manager at ICON, you will be responsible for leading and managing projec

Reference

JR138665

Expiry date

01/01/0001

Rajvir Samra

Author

Rajvir Samra
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Belgium, Mechelen

Location

Mechelen

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are looking for an experienced Clinical Research Associate (CRA) based in Belgium, for our client located in Vilvoorde.Although you are homebased as a CRA, the team regularly meets in the offices i

Reference

JR137717

Expiry date

01/01/0001

Vanessa Verdickt Read more Shortlist Save this role
Statistical Programmer II

Salary

Location

India, Bangalore

Location

Bangalore

Bengaluru

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Programming

Job Type

Permanent

Description

We are currently seeking a Statistical Programmer II to join our diverse and dynamic team. As a Statistical Programmer II at ICON, you will play a vital role in the development, validation, and execut

Reference

JR138352

Expiry date

01/01/0001

Himangshu Skekhar Das Read more Shortlist Save this role
Clinical Site Associate

Salary

Location

Turkey, Ankara

Department

Clinical Monitoring

Real World Solutions

Location

Ankara

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As a CSA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, c

Reference

JR137245

Expiry date

01/01/0001

Jacek Jaworski Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above