PV AssociateLiterature
PV AssociateLiterature
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Job Description
- Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoring
- Contributes to achieving companys goals and objectives
- Ensures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the highest quality and in compliance with global regulations and company policies and in accordance with any Pharmacovigilance (PV) agreement.
- Works under supervision of more experienced colleague
- To assist with the development of literature search strategy
- To participate in weekly and ad hoc literature searches
- To participate in weekly and ad hoc literature screening activities to identify potential ICSRs and other relevant safety related information pertaining to nominated products
- To assist with ordering copies of full literature articles for review
- To maintain a record and track all literature abstracts screened and full literature article reviewed with actions taken and the reason
- To forward any ICSRs to PV Associates for data entry into the global drug safety database
- File other relevant safety related information for use in signal detection and PSURs
- To participate in the screening of local nonindexed literature as required
- To assist in peer review QC of abstracts
- Accessing EV on daily basis and downloading MLM search and MLM ICSR results (excel spreadsheets)
- Tracking all the MLM search results MLM ICSRs list downloads and exported ICSRs
- Uploading the MLM search results and the list of ICSRs in the designated PrimeVigilance Portal area
- Reviewing the list of ICSRs daily
- Checking all urgent/immediate issues have been addressed in a timely manner;
- Keeping the EMA MLM Literature Screening Tracker up to date with the latest information received from the EMA
- Reporting to the unit head and more senior unit team members and providing them with regular updates regarding project status and metrics concerning enquiries
- To assist with the development and improvement of literature screening processes and procedures
- Assisting in departmental regulatory inspection preparedness for the company PV system in the EU and actively participating in PV inspections or audits
Qualifications :
Life science / bio medical background healthcare related degree (chemistry biology biotechnology veterinary science) previous experience is not required.
People who are excited to learn and contribute to patient safety
Time and issue management delegation organization and multitasking skills with good attention to detail
Strong interpersonal and communication skills
Advanced English skills both verbal and written at least B2
Additional Information :
We prioritize diversity equity and inclusion by creating an equal opportunities workplace and a humancentric environment where people of all cultural backgrounds genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly supportive working environment
Opportunity to work with colleagues based all over the world with English as the company language
Our core values are key to how we operate and if you feel they resonate with you then PrimeVigilance could be a great company to join!
Quality
Integrity & Trust
Drive & Passion
Agility & Responsiveness
Belonging
Collaborative Partnerships
We look forward to welcoming your application.
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
