Dein persönlicher KI-Karriere-Agent
Principal Medical Writer – Clinical Pharmacology(m/w/x)
Authoring full Phase 1 Clinical Study Reports and regulatory modules (2.7.1/2.7.2) at a global CRO. Strong experience with Phase 1 CSR and Module 2.7.1/2.7.2 writing required. Flexible remote work.
Anforderungen
- Strong experience in full CSR writing for Phase 1 clinical pharmacology studies
- Strong experience in protocol writing and Module 2.7.1/2.7.2 (SBAAM/SCP) writing
- Proficiency with Word templates and document formatting
- Experience authoring Health Authority responses
- Proficiency in Word templates and document formatting
- Excellent oral and written communication skills in English
Aufgaben
- Write full Clinical Study Reports (CSRs) for Phase 1
- Develop protocols
- Prepare regulatory modules (2.7.1/2.7.2)
- Ensure deliverables are inspection-ready
- Ensure compliance with regulatory and internal guidelines
- Maintain central planning for document writing
- Maintain central planning for QC deliverables
- Recommend process improvements to enhance team collaboration
- Drive document shell creation
- Drive quality control (QC) processes
- Drive timeline management
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Word
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Principal Medical Writer – Clinical Pharmacology(m/w/x)
Authoring full Phase 1 Clinical Study Reports and regulatory modules (2.7.1/2.7.2) at a global CRO. Strong experience with Phase 1 CSR and Module 2.7.1/2.7.2 writing required. Flexible remote work.
Anforderungen
- Strong experience in full CSR writing for Phase 1 clinical pharmacology studies
- Strong experience in protocol writing and Module 2.7.1/2.7.2 (SBAAM/SCP) writing
- Proficiency with Word templates and document formatting
- Experience authoring Health Authority responses
- Proficiency in Word templates and document formatting
- Excellent oral and written communication skills in English
Aufgaben
- Write full Clinical Study Reports (CSRs) for Phase 1
- Develop protocols
- Prepare regulatory modules (2.7.1/2.7.2)
- Ensure deliverables are inspection-ready
- Ensure compliance with regulatory and internal guidelines
- Maintain central planning for document writing
- Maintain central planning for QC deliverables
- Recommend process improvements to enhance team collaboration
- Drive document shell creation
- Drive quality control (QC) processes
- Drive timeline management
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Word
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
IQVIA
Branche
Pharmaceuticals
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
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