Manager, Study Start Up
- Netherlands
- Study Start Up
- ICON Strategic Solutions
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are looking for candidates based in Belgium or the Netherlands who are speaking fluently Dutch.
GENERAL POSITION SUMMARY:
Working directly with Investigative Sites, this role will manage and perform activities at a site level associated with study start‐up including regulatory document collection, preparation of ethics submission documents, informed consent review and essential document package review. Reporting to the SAM Line Manager, the Site Activation Manager must have an in‐depth understanding of study start‐up activities and associated regulatory requirements.
KEY RESPONSIBILITIES:
- Build and cultivate relationships with key study personnel, including Study Coordinators
- Work directly with Investigative Sites for all aspects of study start‐up including: activation timeline development, regulatory document preparation and collection, assisting with IRB/EC submissions and informed consent review
- Assist in creation, review and customization of country/site specific Informed Consent Forms
(ICFs)
- Assist in drafting and responding to IRB queries and facilitating responses to EC queries
- Assist in contract and budget negotiations, as necessary
- Manage translations of relevant study documents
- Proactively identify site challenges and implement appropriate mitigations
- Provide regular local status updates to study team and escalated risks to timelines
- Manage and track issues and escalations to internal stakeholders
- Assist in the development of start‐up plans
- Update study‐tracking tools and databases with site status
- May participate in feasibility and/or site identification activities
- Performs other duties as assigned
KEY COMPETENCIES REQUIRED:
Ability to work under pressure to meet deadlines
Self‐motivated and ability to work well independently and in a team environment
Ability to effectively manage a high volume of multiple priorities
Excellent communication skills (written and verbal) to be able to interact with internal client groups (legal, medical monitors, clinical safety, regulatory affairs and others) as well as external groups (IRBs, Investigators, and others)
Excellent project management skills
Excellent collaboration skills in a cross‐functional environment
Provides input and executes department initiatives
Meticulous attention to detail and process oriented
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
ICON, including subsidiaries, 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, colour, 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 or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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
Similar jobs at ICON
Salary
Location
Colombia, Bogota
Location
Bogota
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Senior Study Start Up Associate to join our diverse and dynamic team. As a Senior Study Start Up Associate at ICON, you will be working within a large-scale, fast-paced envi
Reference
JR141987
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Poland, Warsaw
Location
Warsaw
Gdansk
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinica
Reference
JR141931
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara DrozdowskaSalary
Location
Spain, Madrid
Location
Madrid
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Study Support Assistant, you’ll play an important role in helping our clinical studies get up and running efficiently. This is an ideal position for someone looking to begin a career in clinical
Reference
JR137366
Expiry date
01/01/0001
Author
Persis DavisAuthor
Persis DavisSalary
Location
Japan, Osaka
Location
Osaka
Tokyo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
当社では、IPH・IBT・ICO の Site Activation 業務を横断的に統合し、日本の臨床試験環境の変革を推進するための FSA(Feasibility / Site Activation)ディレクター を募集しています。■ポジション概要 本ポジションは、各部門に分散していた Feasibility / Site Activation 機能を統合し、最適なプロセス設計、効率的なリソース
Reference
JR133204
Expiry date
01/01/0001
Author
Hiroyuki OtsukaAuthor
Hiroyuki OtsukaSalary
Location
Minnesota
Location
Minnesota
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
Through coordination with the Contract & Budget team, and collaboration with divisional and regional clinical teams, the SSU Associate II conducts clinical trial site start-up activities related to th
Reference
JR141979
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
Minnesota
Location
Minnesota
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
Through coordination with the Contract & Budget team, and collaboration with divisional and regional clinical teams, the SSU Associate II conducts clinical trial site start-up activities related to th
Reference
JR141978
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica Hawkins