Senior Director/Director Project Management - Rare Diseases
TA Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please see similar roles below...
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.
The Director/Senior Director will join our CNS/Rare diseases group where you will be adding value through delivering successful client relationships, upholding and working towards a culture of project group excellence.
The Role:
* Develop full service project plans for portfolio of studies and subsequently lead cross functional study teams in accordance with contractual timelines, client specifications and Good Clinical Practices (GCPs).
* Operate at the forefront in this exciting field, supporting projects in the Rare Diseases field
* Effectively lead study budgets to ensure financial targets are met through regular review of indirect costs and project resources
* Inspire and develop your team through people management; co-ordinate study activities against targets, provide coaching and mentoring to Project Managers
* Demonstrate your executive presence, delivering updates on the portfolio to senior management
* Building an environment to enable employees, add towards our culture and engage with the group success
You will need:
* A Bachelor's Degree in medicine, science or equivalent experience in the Clinical Research field and you have the therapeutic experience in across a wide array of complex indications.
* Minimum of 10 years Project Management experience
* A track record of successfully leading large, global cross functional projects; strong domestic and international project management experience
* High level of integrity and can inspire to the demands of the highest standards from a professional and ethical perspective
* Experience of working with rare diseases and ideally with experience in biotech
Why join us?
* You will be working to accelerate the delivery of new therapies to patients
* Ongoing development as a Project Director and the opportunity to progress your career, with the potential to move into other related areas to improve your skill set
* You will have creative resources to be successful in delivering results, inspiring others and becoming a trusted partner
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.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
Teaser label
Our PeopleContent type
BlogsPublish date
03/27/2024
Summary
Exploring Lucy's Path: From Science to Communications Lucy's career journey is a testament to the power of adaptability and seizing opportunities as they arise. "I've been in Clinical Research si
Teaser label
Career ProgressionContent type
BlogsPublish date
03/27/2024
Summary
Interviews can be nerve-wracking experiences, but with the right preparation, you can enter the room with confidence and increase your chances of success. Preparing for an interview is crucial a
Teaser label
Career ProgressionContent type
BlogsPublish date
03/27/2024
Summary
Clinical research plays a crucial role in advancing medical knowledge and improving patient care. At the heart of every successful clinical research study is a Clinical Research Coordinator (CRC
Who we are
Similar jobs
Salary
Location
Czech Republic, Prague
Department
Clinical Monitoring
Location
Prague
Remote Working
Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Join the innovation wave – ICON plc seeks dynamic Clinical Research Associate(CRA) in the Czech RepublicICON plc is a world-leading healthcare intelligence and clinical research organisation. From mol
Reference
JR118157
Expiry date
01/01/0001
Author
Tereza SvobodovaAuthor
Tereza SvobodovaSalary
Location
Romania, Bucharest
Department
Clinical Monitoring
Real World Solutions
Location
Bucharest
Remote Working
Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
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 I
Reference
JR117494
Expiry date
01/01/0001
Author
Denitsa KrastevaAuthor
Denitsa KrastevaSalary
Location
Czech Republic, Prague
Department
Clinical Monitoring
Location
Prague
Remote Working
Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Job Advert missing.
Reference
JR113944
Expiry date
01/01/0001
Author
Tereza SvobodovaAuthor
Tereza SvobodovaSalary
Location
Paris
Department
Clinical Operations Roles
Location
Paris
Business Area
ICON Strategic Solutions
Job Categories
Contracts Administration
Job Type
Permanent
Description
The Contract Specialist we are looking for will be responsible for overseeing specific clinical contract activities. The primary responsibilities include providing contract process guidance, conductin
Reference
2024-109449
Expiry date
01/01/0001
Author
Theo LambertAuthor
Theo LambertSalary
Location
United Kingdom
Department
Clinical Trial Management
Location
UK
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
UK homebased Clinical Trial Manager performing Clinical Risk Manager (CRM) dutiesAre you an experienced Clinical Research or Clinical Project Manager with a flair for innovation, team leadership and e
Reference
2024-109448
Expiry date
01/01/0001
Salary
Location
Belgium, Mechelen
Department
Clinical Monitoring
Real World Solutions
Location
Mechelen
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
JR117574
Expiry date
01/01/0001
Author
Jakob SchonbergerAuthor
Jakob Schonberger