Job Description
We are seeking a talented Clinical Database Designer to join our team. This is an exciting opportunity for someone who wants to work on the design of clinical studies, edit specifications, and system configurations.
Job Description
As a Clinical Database Designer, you will be responsible for interpreting study protocols, designing and updating eCRFs, creating and updating Edit Specification Documents, generating specifications for EDC build components, and completing Study Authorization Forms and Trial Capacity Request Forms.
You will also be attending Pre-Design Meetings, Online Screen Review Meetings, Unblinded Data Review Meetings, Internal Design Review Meetings, and Edit Specification Review Meetings. Additionally, you will facilitate discussions regarding Edit Specification Documents, design databases to collect LLRR data within the InForm database, and ensure Rights and Roles documents have appropriate access for Entry and Updates.
Your responsibilities will include communicating project risks to the Data Team Lead, escalating potential quality issues, ensuring completion and documentation of project-specific training, and staying current with required Standard Operating Procedures.
Required Skills and Qualifications
To be successful in this role, you will need a Bachelor's Degree in Science, Computer Science, Information Technology, or a related field, as well as 0-2 years of relevant core Technical Designer experience and a total experience of 5+ years.
Benefits
As a Clinical Database Designer at IQVIA, you will have the opportunity to work on cutting-edge projects, collaborate with a talented team of professionals, and contribute to the development of innovative medical treatments that improve patient outcomes and population health worldwide.
Job Description
As a Clinical Database Designer, you will be responsible for interpreting study protocols, designing and updating eCRFs, creating and updating Edit Specification Documents, generating specifications for EDC build components, and completing Study Authorization Forms and Trial Capacity Request Forms.
You will also be attending Pre-Design Meetings, Online Screen Review Meetings, Unblinded Data Review Meetings, Internal Design Review Meetings, and Edit Specification Review Meetings. Additionally, you will facilitate discussions regarding Edit Specification Documents, design databases to collect LLRR data within the InForm database, and ensure Rights and Roles documents have appropriate access for Entry and Updates.
Your responsibilities will include communicating project risks to the Data Team Lead, escalating potential quality issues, ensuring completion and documentation of project-specific training, and staying current with required Standard Operating Procedures.
Required Skills and Qualifications
To be successful in this role, you will need a Bachelor's Degree in Science, Computer Science, Information Technology, or a related field, as well as 0-2 years of relevant core Technical Designer experience and a total experience of 5+ years.
Benefits
As a Clinical Database Designer at IQVIA, you will have the opportunity to work on cutting-edge projects, collaborate with a talented team of professionals, and contribute to the development of innovative medical treatments that improve patient outcomes and population health worldwide.
💡 Quick Summary
Seeking a career-building opportunity? The Clinical Database Specialist position is now open for candidates interested in the Database Administrator sector. This role in India offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Database Administrator is a plus.
