Job Description:
- Assure and exert activities leading to effective cooperation with clients in the area of literature monitoring.
- Ensure that Literature Screening responsibilities and activities are managed cost-efficiently, with the highest quality, in compliance with global regulations, company policies, and Pharmacovigilance (PV) agreements.
- Assist with the development of literature search strategies.
- Participate in weekly and ad hoc literature screening activities to identify potential ICSRs and other relevant safety-related information for nominated products.
- Assist with ordering copies of full literature articles for review.
- Maintain a record and track all literature abstracts screened and full literature articles reviewed, including actions taken and reasons.
- 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.
- Participate in the screening of local non-indexed literature as required.
- Assist in peer review QC of abstracts.
Qualifications:
- Life science/biomedical background – healthcare-related degree (chemistry, biology, biotechnology, veterinary science). Previous experience is not required.
- Strong 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 level.