Patient Recruitment Planning Manager
About the role
This vacancy has now expired. Please click here to view live vacancies.
- Recognize, exemplify and adhere to ICON's values which center 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 10%) domestic and/or international.
- Oversight of the Recruitment Planning groups' input into pre-award and awarded studies to ensure consistent standard of deliverable and process adherence across the group.
- Input into and development of Recruitment Planning processes and procedures including templates and job aids to support the Recruitment Planning group and development and delivery of training materials to support these processes across both pre-award and awarded stages.
- Develop strategic relationships with designated Recruitment vendors to ensure effective communication channels and processes at both pre-award and awarded study stages.
- Provide strategic support and act as a functional lead I technical expert on all aspects of Recruitment and Retention Planning for proposals including reaching out to appropriate Recruitment vendors and the provision of internal and pass-through budgets.
- Support, preparation and attendance at Bid Defense meetings in support of ICON business development opportunities
- Attendance at Kick-off meetings, project meetings as required to input into and discuss recruitment and retention strategies.
- Development of study and country recruitment and retention strategies and tactics customized to the need of the study and or sponsor in a format appropriate to be incorporated into the Study Recruitment Plan
- Input into the Site ID questionnaire, or specific recruitment questionnaire (dependent on study/ sponsor requirements), in collaboration with internal and external team members to ensure that the appropriate recruitment and retention questions are addressed and thereafter oversee and manage the process of transitioning the data from site survey through to setting up study specific recruitment plans in awarded projects
- Contract review - ensure specifications are in line with plan. Ensure contract or RAP/Start up agreement in place prior to study start
- Manage the implementation of global patient recruitment campaigns including the development of materials, management of internal and external resources, media campaigns and design and execution in line with the project scope
- Manage/Discuss any strategy or scope changes with the Sponsor/PM in relation to the Recruitment Planning
- Ensure study information saved to Recruitment and Retention eRoom appropriately - including but not limited to, presentations, text, disease information, examples of materials I tactics and any tracking.
- Maintain communication and relationships between all the relevant internal and external parties to ensure all intelligence is utilized in order to make best recruitment planning decision. Review and management oversight of Recruitment Vendors and set up/negotiate Master Services Agreements.
- Assist with the training I mentoring of assigned team members in the principles and conduct of the services offered by the Patient Recruitment Planning group, the system used to support these services and adherence to SOPs and ICON system compliance.
- Line management of all assigned Managers and I or Specialists within the Patient Recruitment Planning group and leadership of the team including being able to effectively manage a remote global Recruitment Planning team.
- Offering assistance and mentoring to team members to create a supportive working environment, developing effective working relationships with the team to enable an atmosphere of motivation, creativity and innovation whilst providing opportunities for future grown and career development within the team.
- Act as a mentor to team members and encourage and train others to mentor more junior staff as part of their personal development and to lead by example and set high standards that others will follow.
- 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.
- Have a background in medicine, science or other relevant discipline with substantial international experience in clinical drug development across a broad range of therapeutic areas
- Good commercial awareness of current practices and trends Recruitment Planning across the industry
- US/LATAM/CAN: A minimum of 7 years industry experience with a minimum of 5 years' experience in recruitment planning in addition to a minimum of 5 years' experience across a broad range of therapeutic areas as a manager and I or project manager.
- EU/APAC: In depth proven experience in industry with in depth proven experience in recruitment planning in addition to experience across a broad range of therapeutic areas as a manager and I or project manager.
- Excellent communicator, both in written and spoken language. Able to produce reports and project plans to a high standard in addition to being able to review the quality and content of reports produced by the Recruitment planning Team. Fluent in English is essential
- Well-developed negotiation skills with the ability to liaise successfully with senior management, clinical project teams, other ICON departments and clients. As well as to influence and present to both small and large groups.
- Competent computer skills in MS Word, Excel and PowerPoint
- Highly developed organizational, problem solving and analytical skill, with the ability to prioritize time sensitive tasks and work independently, to make decision and to progress projects
- Able to milt-task and work well within high pace pressurized environment
- Due to the nature of this position it may be required for the employee to travel. Therefore, dependent
- on the employee's location, the employee may be required to possess a valid Driver's license
- Bachelor's degree, or local equivalent, in a life-science, scientific discipline, medical and I or communication or business studies.
- A higher level degree is preferred.
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. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
06/06/2025
Summary
Building Connections that Drive Progress In an industry where collaboration is critical to advancing science and improving patient outcomes, networking is more than a professional courtesy - it’s
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/29/2025
Summary
Blood Cancer Day Blood Cancer Day is a powerful reminder of the millions of individuals and families whose lives are affected by hematological malignancies every year. These diseases are complex,
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/22/2025
Summary
World Schizophrenia Awareness Day 2025 Every year on 24 May, World Schizophrenia Awareness Day offers a vital opportunity to raise awareness, dismantle stigma, and celebrate the strength of individ
Similar jobs at ICON
Salary
Location
Japan, Tokyo
Location
Osaka
Tokyo
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Liasion
Job Type
Permanent
Description
ICON’s field-based Clinical Trial Liaisons are highly trained site engagement specialists who support clinical trials by providing scientific and clinical support to investigators and site staff to en
Reference
JR128617
Expiry date
01/01/0001
Author
Haruna YamabayashiAuthor
Haruna YamabayashiSalary
Location
France
Department
Clinical Trial Management
Location
France
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
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
2025-119954
Expiry date
01/01/0001
Author
Dominique CarilienAuthor
Dominique CarilienSalary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Logistics & Supplies
Job Type
Permanent
Description
As a Clinical Packaging Technician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This is a Monday- Friday - First shi
Reference
2025-119723
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Canada
Department
Clinical Operations Roles
Location
Canada
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Senior Clinical Trial Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119978
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
United States
Department
Clinical Operations Roles
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Contracts Administration
Job Type
Permanent
Description
As a Sr. Site Contract Management Associate - you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This is a remote role wit
Reference
2025-119982
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Brazil
Department
Clinical Monitoring
Location
Brazil
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
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
2025-119862
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna Duarte