Medical Data Reviewer
- Mexico City
- ICON Full Service & Corporate Support
- Medical Data Review
- Remote
Talent Acquisition Business Partner
- Full Service Division
About the role
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ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With our patients at the center 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.
We have an exciting opportunity for a Medical Data Reviewer to join ICON Biotech’s Medical Affairs team.
LOCATION: Mexico (home-based)
OVERVIEW OF THE ROLE:
The Medical Data Reviewer (MDR), in close cooperation with the Medical Director (MD), sets up and coordinates the medical data review process, conducts medical data review and manages medical queries. The MDR role requires a close collaboration with various members of the Clinical Data Science, Project Management, and Clinical Delivery teams. Specifically, the MDR reviews medical data for consistency and medical plausibility and ensures that the data is comprehensive from a medical point of view across different studies and projects.
- Prepares listings with medical data for medical review for plausibility and consistency
- Drafts the Medical Data Review Plan (MDRP) and medical line items of the Integrated Data Review Plan (IDRP)
- Assures MDRP consistency with other project plans (i.e. DMP), contracted scope of work, and ICON SOPs and procedures
- Together with the ICON MD, reviews the electronic Case Report Form (eCRF), and CRF Completion Guidelines (CCG)
- Manages CRF queries in cooperation with ICON MD, Sponsor and other departments
- Participates in or attends internal and client Kick-Off meetings
- Reviews the protocol together with the ICON MD to determine which standard outputs will be appropriate for medical review and decides whether any customized outputs are needed per study specific requirements
- Reviews and approves all test outputs for medical data review in collaboration with the ICON MD and Clinical Data Science team
- Plans and coordinates the medical review cycles and runs standard/customized outputs as needed according to timeline
- Conducts medical review of the data as per MDRP and IDRP in close collaboration with ICON MD, using pre-established criteria to assure that the data is medically plausible and to clarify inconstancies and missing Adverse Events (AE)
- Ensures a structured medical query management
- Raises and responds to medical queries, following through until query resolution.
Reviews data for protocol deviations - Solves technical problems, reaching out to the Clinical Data Science and Clinical Delivery teams for support as needed
- Ensures that all medical data review activities are completed within the agreed timelines and meet defined quality standards
- Files the MDR related documentation and communication in the TMF, per approved project plans and filing guidance
- Reviews and responds to Quality Control (QC) and audit findings in close cooperation with the ICON MD and People Leader, as needed
- Supports business development activities by providing input into feasibility activities related to medical data review
- Coaches and mentors more junior medical team members, as needed
TO BE SUCCESSFUL, YOU WILL NEED:
- 2+ years of relevant clinical trial industry experience (either in a CRO, sponsor, or clinical site)
- Bachelor’s degree in healthcare/medical field (Nursing, Pharmacist, Medicine, etc.)
- Knowledge of medical terminology and coding systems
- Advanced reading, writing, and verbal English communication skills
- Time management skills with a strong ability to prioritize
- Comfortability working on multiple projects simultaneously
- Strong attention to detail
BENEFITS OF WORKING IN ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.
In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
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, 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.
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Who we are
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Salary
Location
Poland, Warsaw
Department
Full Service - Biometrics
Full Service - Early Clinical and Bioanalytical Solutions
Location
Budapest
Warsaw
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical Data Review
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
JR117664
Expiry date
01/01/0001
Author
Caroline LockAuthor
Caroline Lock