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We are currently partnered with one of our leading global health care clients who are seeking Clinical Database Developer on a remote basis in Canada
Job Summary :
- Develops programming / configuration of Veeva and Medrio CRFs, folders, edit checks, derivations, integrations, migrations, and reports, based on protocol requirements.
- Sets up Coder, Local Lab, Targeted SDV modules.
- Leads eCRF design and review meetings.
- Provides user support and technical support and conduct end user training
Key Information :
The Clinical Database Developer will collaborate closely with data management and statistical teams to design and develop electronic case report forms (eCRFs), visit schedules, and data quality checks for medical research studies. This role requires working in a dynamic, team-oriented environment to create and implement solutions, including system development, testing, and integrations.
While the primary focus will be on Veeva CDMS, the Clinical Database Developer may also be responsible for building case report forms using other electronic data capture (EDC) systems, such as Medrio or Rave.
All activities must be performed in compliance with applicable regulatory requirements, industry guidelines, and standard operating procedures (SOPs), while ensuring alignment with sponsor expectations and project timelines.
About Planet Pharma :
Planet Pharma is an American parented Employment Business / Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including : Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion / belief, sexual orientation or age.