Literature Review Advisor

Job Title: Literature Review Advisor

Location-

Hybrid opportunity!

Notice period-

Experience-

Introduction to role

:Are you ready to make a difference in the pharmaceutical industry As a Literature Review Advisor, you'll be at the forefront of ensuring the quality and accuracy of comprehensive literature reviews within the pharmaceutical sector. Working closely with the local PS team, you'll provide technical and operational support to the Literature Review Team, ensuring compliance with company and regulatory standards. Your role will involve building relationships with internal and external collaborators, supporting drug development, regulatory submissions, and clinical practice through insightful literature-based analysis. Dive into a dynamic environment where your analytical skills and understanding of pharmaceutical research methodologies will shine

!Accountabilities

• :Literature Review Procedure
• sEnsure the quality and comprehensiveness of literature searches, including the use of AstraZeneca databases
• .Conduct reconciliations ensuring the accuracy of pharmacovigilance data that is transferred and received
• .Oversee the identification, collection, and analysis of relevant scientific publications, clinical studies, and regulatory reports
• .Keep up to date with industry developments, particularly automation and technology changes, to ensure AstraZeneca leads the way in conducting literature searches
• .Collaboration & Cross Functional Suppor
• tCollaborate with cross-functional teams (Marketing Company collaborators, R&D, regulatory, medical affairs, clinical operations) to provide literature-based insights that inform drug development and regulatory strategies
• .Work closely with subject matter experts to develop clear, concise, and scientifically sound literature materials, summaries, and reports
• .Collaborate with external collaborators and/or academic institutions on literature review-related tasks
• .Regulatory & Compliance Adherenc
• eActively contribute to maintaining the core components of Good Pharmacovigilance Practice by contributing to all safety-related processes and brand activities within countries of remit and being audit and inspection ready
• .Support external service providers to meet company and local regulatory PV requirements
• .Complete all required patient safety trainings in adherence to internal processes and external regulations, obtaining access to relevant systems such as Safety Database, Regulatory systems, Human Resources systems, Quality Management Systems, and other global or local systems commercial databases as appropriate
• .Maintain current and in-depth knowledge of
• :Global and local procedural and guidance documents
• .Marketed status of products in the local country and reference documents (i.e., Core Data Sheet)
• .Conditions, obligations, and other commitments relating to product safety or the safe use of AstraZeneca products

.Essential Skills/Experience

• :Pharmacovigilance knowledge excellenc
• eGood Pharmacovigilance Practic
• eKnowledge of health authority's regulation
• sCross functional collaborative approac
• hEffective and lateral thinkin
• gProblem solvin
• gVendor managemen
• tExcellent attention to detai
• lExcellent written and verbal communication skill

sDesirable Skills/Experience

• :Influencing and Conflict Resolution skill
• sMedical knowledge in company Therapeutic Area
• sProject managemen
• tSuccessful participation in above-market project
• sAudit & Inspection experienc