Site Manager (Senior CRA)
- Belgium, Netherlands
- Clinical Monitoring
- ICON Strategic Solutions
- Remote
TA Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please see similar roles below...
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, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
For our client in the Antwerp region, we are looking for a Senior Clinical Research Associate (Snr Site Manager) to join our ICON team! You will be working for one of the most attractive employers in Belgium, creating a real impact on the health of patients worldwide.
As a Senior CRA your main responsibilities will be to provide trial coordination and site management services for your assigned studies/sites. For this you will independently ensure that your sites are inspection read at all times, perform pretrial assessment,site selection, subject recruitment and retention planning, site initiation, monitoring and close-out.
Key responsibilities:
- Perform site qualification, site initiation, and closeout visits, ensuring regulatory and protocol compliance. Visits may be on-site or remote.
- Generate queries and manage resolutions with site personnel.
- Document activities via confirmation letters, follow-up letters, trip reports, communication logs and other required study documents as per SOPs and Study Monitoring Plan.
- Perform investigational product accountability as per the protocol and Study Monitoring Plan.
- Ensure to set up proper recruitment/maintenance plan based on appropriate analysis of capability of sites selected.
- Act as primary liaison with site personnel.
- Management and collection of site's study regulatory documents.
- Enter data into tracking systems as required.
- Assist and support audit preparation and CAPA implementation.
- AE/SAE and expedited reporting and management.
Requirements
- Degree in a health or sciences related field
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
- Proven experience in on-site monitoring of clinical studies is a must. Minimum experience of 3 years.
- Demonstrated proficiency in problem solving, juggling multiple priorities and a commitment to quality and customer focus.
- Proven ability to work independently in a fast-paced environment.
- Strong communication, interpersonal, and organizational skills.
- Must demonstrate good computer skills.
- Fluently Dutch, French and English
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.
#LI-Hybrid
#LI-VV1
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
![A picture of Debora Oh](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2023.17000.2380/img/Oi_Ywfaw1E2c5AjadgdpUA/75/debora-oh-thumbnail.jpg)
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
![A picture of Yemi Moses](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2023.17000.2380/img/voIjKGzvOUdxWAjadgXIBA/75/yemi-moses-thumbnail.jpg)
Teaser label
Our PeopleContent type
BlogsPublish date
05/23/2023
Summary
How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce
![A picture of Suzaita](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2023.17000.2380/img/x7o-Djy2R0cv_gjbLGx6Ig/75/Suzaita.png)
Teaser label
A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?
by
Suzaita Hipolito
Who we are
Press play to find out more
![](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2023.17000.2380/Blob/img/full-width-video.jpg?v=2023.15273-main)
Similar jobs at ICON
Salary
Location
Beijing
Department
Clinical Monitoring
Location
Beijing
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 organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2024-111232
Expiry date
01/01/0001
Author
Sally ZengAuthor
Sally ZengSalary
Location
Zhengzhou
Department
Clinical Monitoring
Location
Zhengzhou
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Clinical Research Associate Zhengzhou h
Reference
2024-111051
Expiry date
01/01/0001
Author
Xiangilan LiuAuthor
Xiangilan LiuSalary
Location
ShenYang
Department
Clinical Monitoring
Location
ShenYang
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Clinical Research Associate Shenyang ho
Reference
2024-111050
Expiry date
01/01/0001
Author
Xiangilan LiuAuthor
Xiangilan LiuSalary
Location
Guangzhou
Department
Clinical Monitoring
Location
Guangzhou
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Clinical Research Associate
Reference
2024-110354
Expiry date
01/01/0001
Author
Sunshine YangAuthor
Sunshine YangSalary
Location
Chengdu
Department
Clinical Monitoring
Location
Chengdu
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 organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2024-111301
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Brazil
Department
Clinical Monitoring
Location
Brazil
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As the Senior Manager – Pharmacovigilance, you will be responsible for overseeing a large team of PV professionals, for an assigned FSP client program. Reporting into the Director of Clinical Operatio
Reference
2024-110646
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna Duarte