Senior Director, Project Management - Women's Health
About the role
This vacancy has now expired. Please click here to view live vacancies.
Senior Director, Project Management - Women's Health (Home-based)
At ICON, it's our people that set us apart.
The role
- Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance
- As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs
- Travel (approximately 30%) domestic and/or international
- Line-manage and ensure collaboration within a team of Directors and Project Managers in the planning, execution and governance of projects/portfolios
- Manage the resources to ensure that established cost, time, and quality goals are met
- Manage development, provide direction and support, and mentor PMs/PDs and/or their managers as needed
- Provide technical support and guidance (including scope definition , risk identification and mitigation, resource planning, goals and deliverables) to assigned PM staff
- Plan capacity across new/existing PM/PD resources and secure needed resources whilst optimising staff utilisation/recovery
- Keeps Global VP, PM, business sponsors, business-unit leadership and all stake-holders regularly informed of project/program progress, risks and issues through periodic reporting
- Ensure all necessary training is provided to assigned staff to improve their job performance and knowledge
- In conjunction with colleagues and senior management , responsible for setting agenda and developing training philosophy for ICON PM group, including successful execution throughout the team
- Ensure team alignment with cross-functional leadership goals and company initiatives
- Measure and report PM KPls and lead continuous improvement
- Contribute to the ICON PMO model built on strong teamwork , frequent and transparent inter and intra divisional communication , continuous process improvement, metrics management and global team harmonization
- Act as the key client contact for designated clinical projects/programs , and develop successful relationships with clients to drive increased volume of business. This includes active participation in client operations committee or executive committees as necessary.
- Demonstrate understanding of drug development including planning and delivery for a product (drug asset) through multiple phases of development.
What you 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 Women's Health indications.
- Minimum of 12 years Project Management experience
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
- Working knowledge of project management technique and tools
- Direct work experience in a global, cross-functional project management environment
- Proven experience in people management
- Proven experience in strategic planning, risk management and change management
- Ability to work closely with business unit leadership to understand customer's needs
- Strong analytical skills and business acumen
- Executive presence with ability to confidently deliver complex presentations to senior management
- Willingness to travel up to 25% as needed
- You will be working to accelerate the delivery of new Women's Health therapies to patients
- Ongoing development as a Senior 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
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
IndustryContent type
BlogsPublish date
04/03/2026
Summary
Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re
Teaser label
Our PeopleContent type
BlogsPublish date
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
Teaser label
Our PeopleContent type
BlogsPublish date
03/24/2026
Summary
Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv
Similar jobs at ICON
Salary
Location
Fort Worth, TX
Location
Fort Worth, TX
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Research Site Services
Job Type
Permanent
Description
As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. Th
Reference
JR148277
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.What You Will Do:You will take responsibil
Reference
JR148292
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna DuarteSalary
Location
Regional United States (PRA)
Department
Full Service - Corporate Support
Location
Multiple US Locations
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Human Resources
Talent Acquisition
Job Type
Permanent
Description
We are currently seeking a Senior Talent Acquisition Business Partner to join our diverse and dynamic team. As a Senior Talent Acquisition Business Partner at ICON, you will be responsible for develop
Reference
JR147826
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
US, Raleigh, NC
Department
Full Service - Corporate Support
Location
Raleigh
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Talent Acquisition
Job Type
Temporary Employee
Description
We are currently seeking a Talent Sourcing Recruiter to join our diverse and dynamic team. As a Talent Sourcing Recruiter at ICON, you will focus on building strong talent pipelines for critical roles
Reference
JR147050
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
US, Raleigh, NC
Department
Full Service - Corporate Support
Location
Raleigh
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Talent Acquisition
Job Type
Temporary Employee
Description
We are currently seeking a Talent Sourcing Recruiter to join our diverse and dynamic team. As a Talent Sourcing Recruiter at ICON, you will focus on building strong talent pipelines for critical roles
Reference
JR147054
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Scientist
Job Type
Permanent
Description
We are currently seeking a Clinical Scientist to join our diverse and dynamic team. As a Clinical Scientist at ICON, you will play a critical role in designing and conducting clinical studies that adv
Reference
JR146888
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna Duarte