Parexel job vacancy for Associate Medical Writer

About the job

Basic experience/understanding of Clinical Trial Disclosure/Clinical Trial Transparency. The candidates with the below experience would be preferred.

Experience handling regulatory websites such as ClinicalTrials.gov, EudraCT/ Clinical Trials Information System (CTIS), and European Union electronic Register of Post-Authorization Studies (EU PAS Register)
Protocol Registration/ Maintenance for ClinicalTrials.gov and EU PAS Register
Results postings for ClinicalTrials.gov, EudraCT/ Clinical Trials Information System (CTIS), and European Union electronic Register of Post-Authorization Studies (EU PAS Register)
Plain language summaries (for distribution to study participants, posting on customer websites or upload onto the EMA portal as per the EU Clinical Trials Regulation 536/2014 [Article 37])
Anonymisation and Redaction (EU-CTR (CTIS), EMA Policy 0070, Health Canada (PRCI), ClincalTrials.gov, EU PAS Register)