ICF Specialist
Sofiaonsitemid
Posted today · via Workday
About this role
Job Overview Under the guidance of Global Clinical Study Support (“CSS”) management, this position will be responsible for review, coordination and finalization of Global Informed Consent Form templates for all sponsor clinical studies that are managed by Development Operations. It could be possible to include also to perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Master ICFs: The reviewer checks the ICF created by the study team against the protocol, the biological samples plan, and other documents to confirm accuracy.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: css
2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Sofia. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
css
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