DOCS Operations Manager
Hi, I am Davidand I manage this role
Talent Acquisition Specialist for EMEA Team
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.
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
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish 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
Inside ICONContent type
BlogsPublish 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
IndustryContent type
BlogsPublish 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
Similar jobs at ICON
Salary
Location
Australia, Sydney
Location
Sydney
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Role: Experienced Clinical Trial ManagerLocation: Sydney (hybrid)As a Clinical Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by he
Reference
JR146418
Expiry date
01/01/0001
Author
Joanne ShinAuthor
Joanne ShinSalary
Location
Canada, Montreal
Location
Montreal
Remote Working
Remote
Business Area
ICON Strategic Solutions
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
JR146393
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Dallas, TX
Location
Atlanta
Houston
Tampa, FL
Dallas, TX
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Project Management
Job Type
Permanent
Description
What You Will Be Doing:Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the
Reference
JR146251
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
Canada, Burlington
Location
Montreal
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. As a CTA at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, i
Reference
JR146002
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a
Reference
JR147014
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
US, Cambridge, MA
Location
Boston
Philadelphia, PA
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Project Management
Job Type
Permanent
Description
What You Will Be Doing:Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the
Reference
JR146133
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan Holmes