UK Clinical Project Manager
- London
- ICON Strategic Solutions
- Clinical Trial Management
Principal Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
An additional UK home-based Oncology Clinical Project Manager is required to manage sites (with some CRA Line Management responsibilities) within the UK region.
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.
You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
Amongst other tasks, your main responsibilities will be to;
- Ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation is archived.
- Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
- Leads and optimises the performance of the Local Study Teams at country level
- Liaison with Senior Management in developing study strategy.
Ideal candidates will be those with Oncology project management experience in the clinical space, with a significant background in clinical research monitoring roles; the candidates operating as Clinical Project Managers would be ideal.
What is Required
- Degree (BA/BS/BSc) in life sciences
- Proven track-record in Oncology Project Management of clinical trials within the Clinical Research industry
- Clinical Project Managers with a CRA background
- Must have demonstrated strong client relationship management skills
- Must be able to manage culturally diverse and practically remote teams
Education and Experience requirements:
Minimum of 4 years progressive experience in clinical operations including project coordination, site management and monitoring with some project management experience or equivalent.
University degree, preferably in a scientific discipline
#LI-Remote
#LI-DB1
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
Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan
Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe
Teaser label
Career ProgressionContent type
BlogsPublish date
07/06/2022
Summary
It's not hard to reel off a list of reasons to become a Medical Director. The chance to ensure that patient care is high-quality will likely be right at the top. But why should you bring your Medical
Similar jobs at ICON
Salary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
What you will be doing: The L-LTM role will be accountable/responsible for ensuring top-quality end-to-end trial delivery at a country level, managing the consistency of Local Trial Management duties
Reference
JR137619
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
France, Paris
Location
Paris
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
JR137592
Expiry date
01/01/0001
Author
Zaklina LomberAuthor
Zaklina LomberSalary
Location
UK, Reading
Location
Barcelona
Reading
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Title - Clinical Risk Surveillance Lead Location - Must be based in the UK or Spain (remote)Sponsor dedicated As a Clinical Risk Surveillance Lead you will be joining the world’s largest & most compre
Reference
JR135967
Expiry date
01/01/0001
Author
Amani YousefAuthor
Amani YousefSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
What you will be doing Work with the clinical trial management staff to support the execution and monitoring of clinical studies and trial deliverables.Participate in study planning and set-up activit
Reference
JR137404
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
South Africa, Johannesburg
Location
Johannesburg
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
JR137509
Expiry date
01/01/0001
Author
Shelley BallAuthor
Shelley BallSalary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
What you will be doing: • Contribute to the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance. • Lead the preparation of country
Reference
JR137206
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan Holmes