Regional Mobile Data Coordinator
TA Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please see similar roles below...
Regional Mobile Data Coordinator (Non-Manager Level) (UK, France, Germany, Spain, Italy and US
Icon plc - Global Oncology Site Network
Discretionary Bonus Scheme
Travel (Approximately 60%) domestic and/or international
Introduction
At ICON, it's our people that set us apart.
Are you looking for an outstanding opportunity to develop your career with a leading edge Global Commercial Oncology Site Network which is growing fast?
As a global provider of drug development solutions, our work is a serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
Our Oncology Site Network concentrates on fast site set up, quick patient enrolment, high data and quality standards, delivering excellent patient experience resulting in a high level of patient retention. These qualities are what our Sponsors look for in a leading Oncology Site Network and you can be part of our success story. We are growing our international footprint and you can play a part in our expansion and be involved in the future of oncology treatments across the globe.
This is an excellent opportunity for a mobile Data Coordinator with exposure to CROs, Research Sites and Networks to play an implemental role in driving our organisation towards success.
As a Data Coordinator, you will be accountable for ensuring all data generated at site has been processed and entered accurately into electronic systems within the set timelines. You will be responsible for data quality and CRA liaison. Able to travel at a short notice both domestically and internationally (Approximately 60%).
Main Responsibilities
Data Management
· Transcribing all data generated at site into electronic systems within the set timelines.
· Maintaining, filing and organising patient source notes and any associated data and files.
· Maintaining, filing and organising Investigator site files and associated documents.
· Ensure all folders are up to date, correctly labelled and stored securely and in an organised manner.
· Working to SOP/COPs and GCP guidelines
Query Resolution, data cleaning and Quality control
- Resolve queries generated by sponsor representatives and electronic systems within the set timelines.
- Liaise with relevant members of the clinical team to resolve queries and improve data quality.
- Maintain high quality standards by regularly checking data for any discrepancies.
- Provide review of source data worksheets during study start up.
- Assist operation compliance team in carrying out any data cleaning activities and internal audits.
- Ensure audit and inspection readiness and assist with preparation of audits and inspections.
- Ensure version control of all documents and liaise with QA team regularly.
Coordinating CRA and other sponsor representative visits
- Book and coordinate CRA visits and phone calls to site for monitoring purposes.
- Address any findings during and after the visit and follow up letters within the set timelines.
- Ensure all files are inspection ready.
Administration
- As a team member at your site you are expected to work closely with Doctors/Nurses and other Site members under the supervision of the Principal Investigator to ensure the best outcome with regards to patient care and quality of service.
To be successful you will need:
- Excellent communication and influencing skills
- Qualification - BSc or MSc preferably in science or biomedical fields
- Bilingual - English with another European language that is widely used in Europe
- Able to travel at short notice - around your home and Europe
- IT skills - fluent and familiar with IT
- Attitude - passionate
- Excellent interpersonal skills and telephone manner
- Pro-active, flexible and able to multi-task
- Good organisational skills with attention to detail
- Able to work under pressure and to deadlines
- Self-motivated
- Travel (Approximately 60%) domestic and/or international
Why join us?
Ongoing development is vital to us, and as one of the Data Coordinators in our Global Oncology Site Network, you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment
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
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
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
JR116519
Expiry date
01/01/0001
Author
Kashifa TahseenAuthor
Kashifa TahseenSalary
Location
Netherlands, Groningen GRQM (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Groningen
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Job Type
Temporary Employee
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
JR116495
Expiry date
01/01/0001
Author
Stephanie Broize-ArrieuAuthor
Stephanie Broize-ArrieuSalary
Location
Japan, Tokyo
Department
Full Service - Project Management
Location
Osaka
Tokyo
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Project/ Program 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
JR114298
Expiry date
01/01/0001
Author
Daiki MatsumotoAuthor
Daiki MatsumotoSalary
Location
Taiwan, Taipei
Department
Clinical Monitoring
Location
Taipei
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
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
JR118189
Expiry date
01/01/0001
Author
Candice WangAuthor
Candice WangSalary
Location
Korea, Seoul
Department
Study Start Up
Location
Seoul
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
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
JR117225
Expiry date
01/01/0001
Author
Daisy ParkAuthor
Daisy ParkSalary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Logistics & Supplies
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
2024-109389
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon Pupek