PK/PD Documentation Specialist (m/w/d)
PK/PD Documentation Specialist (m/w/d)
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Deliver high quality coordination of the centralized support by the document service management group for upload of relevant Clinical Pharmacology & Pharmacometrics (CPP) documents (e.g. population PK/PD data transfer plans population PK/PD analysis plans and population PK/PD reports) within the required regulatory system per global aligned procedures of client. Perform memo and report strawman support document quality control (QC) prepare Clinical Pharmacology & Pharmacometrics documents for submission or health authority interactions provide writing support implement QC process refinement as defined by the Clinical Pharmacology & Pharmacometrics organization and track the operational progress amongst stakeholders. Services are delivered by applying organizational and scientific writing skills to support document writing and QC in line with applicable guidelines and regulations.
Responsibilities
- Clear communication with clinical pharmacology & pharmacometric leaders and other team members.
- Ensure deliverables are inspection ready and compliant with relevant requirements.
- Maintain the central planning of population PK/PD document writing and QC deliverables.
- Provide advice/recommendation on process improvements in support of interactions between Clinical Pharmacology & Pharmacometrics and the document service management group.
- Drive the PK/PD document shell writing document QC process management of deliverable timelines; receive and review documents (e.g. reports) compile comments and edits; follow up on comment resolution in close collaboration with the team.
- Provide PK/PD document QC of reports and manage the review process documentation within QC checklist including comment resolution follow up within projected timelines in line with the analysis plan and internal guidelines.
- Support the development of CPP reporting templates analysis plans data transfer plans as required in close partnership with the document service management group.
Education and Experience Requirements/Qualifications:
- Minimum degree: BA/BS Degree in a health science or computer science related field.
- Strong experience working in Pharmaceutical or CRO Industry
- Proficient with word templates and document formatting.
- Experienced in scientific report writing and document QC procedures.
- Project Management and organizational skills ability to prioritize multiple projects.
- Proficient in speaking and writing in English. Effective communication skills oral and written.
- Experience in population PK/PD report writing and review is preferred.
This role is not eligible for UK visa sponsorship
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Unclear Seniority
Employment Type
Full-Time
