2.0 - 6.0 years

0 Lacs

kochi, kerala

On-site

As a Clinical Database Designer, you will be responsible for various aspects related to study build & design, edit specifications, system configurations, and associated study design components. Your role will involve collaborating with stakeholders such as DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. Additionally, you will also be accountable for project financials from a programming shared services perspective. Your key responsibilities will include interpreting the study protocol, designing and updating the eCRF, and creating/editing the Edit Specification Document. You will be involved in generating specifications for EDC build components, completi...

Posted 1 month ago

AI Match Score

Apply

Programmer Analyst ProcDNA

3.0 - 5.0 years

0 Lacs

Bengaluru, Karnataka, India

On-site

About ProcDNA: ProcDNA is a global rocket ship in life sciences consulting. We fuse design thinking with cutting-edge tech to create game-changing Commercial Analytics and Technology solutions for our clients. We&aposre a passionate team of 300+ across 6 offices, all growing and learning together since our launch during the pandemic. Here, you won&apost be stuck in a cubicle - you&aposll be out in the open water, shaping the future with brilliant minds. Ready to join our epic growth journey What we are looking for We are seeking a Programmer Analyst with strong hands-on experience in EDC platforms such as Medidata RAVE, InForm, Central Designer, or Veeva Studio. The ideal candidate will have...

Posted 2 months ago

AI Match Score

Apply

Clinical Programmer - II (Rave) Syneos Health

4.0 - 6.0 years

8 - 12 Lacs

Hyderabad

Hybrid

Immediate Joiners preferable. Role & responsibilities •Utilizes primary development tools including Oracle RDC, Oracle Inform, Medidata, Rave, SAS, and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures. •Generates and maintains all required documentation, including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports. •Serves on project teams to coordinate and l...

Posted 3 months ago

AI Match Score

Apply

Clinical DB Designer Iqvia Biotech

5.0 - 8.0 years

5 - 8 Lacs

Bengaluru, Karnataka, India

On-site

Interprets the study protocol. Design and update the eCRF. Create and update Edit Specification Document. Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page) Complete the Study Authorization Form and Trial Capacity Request Form (InForm) Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document. Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate acc...

Posted 3 months ago

AI Match Score

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.