Clinical Trial Manager (PMS/IIT)
- South Korea, Seoul
- ICON Strategic Solutions
- Clinical Trial Management
- Remote
TA Business Partner
- Icon Strategic Solutions
About the role
Home-Based, Seoul, South Korea
As a (PMS/IIT - Clinical Trial Manager) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true “one team” approach that provides limitless opportunity to develop through training, mentorship, and support from leadership.
What you will be doing:
The PMS is responsible for the timely reporting and processing of respective Serious Adverse Events (SAE), Adverse Event (AE) Serious and non-Serious Adverse Drug Reaction (SADR) and other medically related project information within agreed timelines to Health Authorities and other Key Stakeholders. They are responsible for document archiving, data tracking communication of respective safety reports in compliance with company’s and relevant regulator’s requirements.
Responsibilities:
- Perform initial review of the adverse event perform seriousness and relatedness assessment and follow up SAE/AE/ADR/SADR queries to investigator sites or reporters
- Liaise with the investigational site and or reporter regarding safety issue
- Ensure accurate entry of safety data into the safety database or relevant system
- May assist the team in create patient adverse event narratives (if appropriate)
- Archive document related to entered safety data and other in accordance with regulatory requirement, respective SOPs and manuals
- Communicate with relevant stakeholder (Health Authority, Site Staff) to clarify enquiry of entered data on the safety database
- May assist the Medical team to train member from other department on how to collect safety information for Spontaneous safety reporting of marketed product to the company
- Assist the team member with safety case monitoring/ Screening activity on safety database
- May attend the project team meeting and teleconference as needed
#LI-Remote
#LI-SO1
You are:
- Computer literacy desirable
- Good oral and written English communication skills
- Bachelor degree, or local equivalent, in medicine, science or related discipline
- At least 2~3 years of PM with Medical affairs studies (RMP, PMS, and IIS)
- Home-Based
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
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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. See all locations Learn more about Our Culture at ICON
Day in the life
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv
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
Teaser label
Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan
Similar jobs at ICON
Salary
Location
Australia
Department
Clinical Trial Management
Location
Australia
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Role: Local Trial ManagerLocation: Australia (home-based) As a Local Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare i
Reference
2024-115899
Expiry date
01/01/0001
Author
Krisztina AuthAuthor
Krisztina AuthSalary
Location
Canada
Department
Clinical Trial Management
Location
Canada
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2024-115860
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
United States
Department
Clinical Trial Management
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Senior Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2024-115826
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Poland, Spain, United Kingdom
Department
Clinical Trial Management
Location
Poland
Spain
UK
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Job title - Clinical Trial Manager Location - UK, nationwide travel Fully Sponsor dedicated As a CTM you will be joining the world’s largest & most comprehensive clinical research organisation, powere
Reference
2024-115707
Expiry date
01/01/0001
Author
Amani YousefAuthor
Amani YousefSalary
Location
Germany
Department
Clinical Trial Management
Location
Germany
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2024-115868
Expiry date
01/01/0001
Author
Alexander SourounisAuthor
Alexander SourounisSalary
Location
London
Department
Clinical Trial Management
Location
London
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
UK home-based (Non-Oncology) Clinical Project Manager is required to manage sites (with some CRA Line Management responsibilities) within the UK region. You will be partnering with a well-known global
Reference
2024-115832
Expiry date
01/01/0001
Author
Dominic BradyAuthor
Dominic Brady