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 of male
Leading Through Change: Zhong Yao's Journey at ICON in China

Teaser label

Our People

Content type

Blogs

Publish date

12/10/2025

Summary

Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.

Teaser label

From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

Read more
Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
View all

Similar jobs at ICON

Clinical Trial Assistance

Salary

Location

Regional United States (PRA)

Location

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Operations

Job Type

Permanent

Description

We are currently seeking a CTA to join our diverse and dynamic team. As a CTA ICON, you will play a pivotal role in supporting the design, implementation, and management of clinical trials, contributi

Reference

JR139998

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Project Specialist

Salary

Location

Regional United States (PRA)

Location

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Project/ Program Management

Job Type

Permanent

Description

We are currently seeking a Research Operations Coordinator to join our diverse and dynamic team. As a Research Operations Coordinator at ICON, you will play a pivotal role in supporting various projec

Reference

JR141111

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Pharmacovigilance Systems Specialist

Salary

Location

India, Chennai

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Pharmacovigilance Systems Specialist to join our diverse and dynamic team. As a Pharmacovigilance Systems Specialist at ICON, you will be responsible for managing and optimi

Reference

JR136739

Expiry date

01/01/0001

Archana Bakkiyarajan Read more Shortlist Save this role
CDC II

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Job Type

Permanent

Description

What you will be doing  Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.Manage clinical and third-party data reconciliation base

Reference

JR135148

Expiry date

01/01/0001

Daniela Guerrero Read more Shortlist Save this role
Pharmacovigilance Associate - Post Marketing (FSP - Sponsor Dedicated)

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety

Reference

JR141138

Expiry date

01/01/0001

Simone Chan

Author

Simone Chan
Simone Chan

Author

Simone Chan
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above