JUMP TO CONTENT

DOCS Operations Manager

JR073408

About the role

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

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

Through combined functional, operational and talent expertise, DOCS offer resourcing solutions and FSP models that significantly improve business performance. This person will effectively manage Contract Placement Consultants (CPCs) who are insourced to a client, ensuring high performance, quality delivery of client objectives and continuous development of DOCS CPCs.

Job Functions and Responsibilities:

The responsibilities of the Operations Manager include, but are not limited to:

  • 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.

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.

Qualifications, Experience & Skills:

  • Bachelor's Degree or local equivalent, in life sciences, medicine or related discipline.
  • Minimum of 5 years of relevant industry experience in either Digital health, data management or medical writing
  • Previous experience in clinical project management or/and line management is preferred but not mandatory.
  • Demonstrated ability to identify, analyze and solve problems.
  • Excellent interpersonal, organizational and management skills.
  • Excellent verbal and written communication skills in English.
  • Strong computer skills.
  • Ability to operate in a multi-cultural environment.

List #1

Day in the life

Headshot image of male
Driving Trials Forward: Study Start-Up Leadership at ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/16/2026

Summary

Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

Teaser label

Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

Read more
Male and female in lab
Who’s Who in a Clinical Trial Team

Teaser label

Inside ICON

Content type

Blogs

Publish date

03/15/2026

Summary

Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

Teaser label

Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

Read more
Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

Teaser label

Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

Read more
View all

Similar jobs at ICON

Clinical Research Nurse I

Salary

Location

US, San Antonio, TX, IDS

Location

San Antonio

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

JR146726

Expiry date

01/01/0001

Stephanie Curran Read more Shortlist Save this role
CRA I / CRA II (Multisponsor)

Salary

Location

Argentina, Buenos Aires

Department

Clinical Monitoring

Location

Buenos Aires

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking CRA I / CRA II (Multisponsor) to join our diverse and dynamic team. You will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data,

Reference

JR140950

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
CRA II

Salary

Location

Argentina, Buenos Aires

Location

Buenos Aires

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli

Reference

JR142578

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
Senior Clinical Trial Manager

Salary

Location

US, Blue Bell (ICON)

Department

Clinical Trial Management

Location

Blue Bell

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic Internal Medicine team. As the Senior Clinical Trial Manager, you will hold a crucial role in ensuring the succ

Reference

JR146821

Expiry date

01/01/0001

Michael Hartley Read more Shortlist Save this role
Pharmacovigilance Associate (Call Center team)

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

Position SummaryThe MI staff member will work in a Medical Call Center and is responsible for all medical information duties to support clients in compliance with applicable regulation, the company St

Reference

JR144500

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
Senior Director, Business Development

Salary

Location

US, Blue Bell (ICON)

Department

Full Service - Commercial Solutions

Location

Blue Bell

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Sales

Job Type

Permanent

Description

We are currently seeking a Senior Director of Business Development to join our diverse and dynamic team. This Business Development role is an individual-contributor sales position dedicated to driving

Reference

JR145956

Expiry date

01/01/0001

Michael Hartley Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above