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A clinical research consultancy is seeking a Plain Language Summary Specialist to develop accessible trial summaries. This remote role involves ensuring EU compliance and collaborating with pharmaceutical teams. Strong medical writing and editing skills are essential, along with a background in life sciences. Join a mission-driven team dedicated to enhancing transparency and patient engagement.
Plain Language Summary (PLS) Specialist – EU CTR Compliance (Remote, UK-based)
Do you have a passion for making clinical research more accessible to patients and the public? Join a fast-growing team dedicated to producing clear, compliant plain language summaries (PLS) in line with the EU Clinical Trial Regulation (CTR).