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Scientist, Clinical Trial Safety

2+ years
Not Disclosed
10 July 24, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Scientist, Clinical Trial Safety

Career Level - C

Introduction to the Role:

Join our innovative team at the Trial Safety Review Center (TRISARC) within the Research and Development function of AstraZeneca. As a Scientist in Clinical Trial Safety, you will play a critical role in ensuring the accuracy and completeness of patient data in clinical trials. This position offers a unique opportunity to collaborate with Senior Scientists, Senior Analysts, and Associate Directors in reviewing crucial medical data.

Key Responsibilities:

In this role, you will support the team during study start-up activities, conduct ongoing reviews of patient-level clinical/safety data, schedule and facilitate various meetings, and create visualizations using applicable tools. Additionally, you will perform quality checks on documents, update study statuses in trackers, and maintain the currency of information on TRISARC platforms.

Essential Skills/Experience:

  • Educational background in Life Sciences (BSc/MSc/PhD) or equivalent work experience in related fields.
  • Knowledge of ICH/GCP Guidelines.
  • Understanding of Serious Adverse Event (SAE) reporting requirements.
  • Strong attention to detail and analytical skills.
  • Ability to manage multiple tasks in a high-volume environment with shifting priorities.
  • Excellent time management skills.
  • Team player with the ability to work independently.
  • Proficiency in computer applications.
  • Excellent verbal and written communication skills in English.
  • Background in pharmacovigilance or experience with clinical studies.
  • Clinical/medical knowledge and practical experience with SAEs and other safety events.
  • Understanding of the clinical study and drug development process.
  • Experience with programming is a plus.

At AstraZeneca, we believe in fostering bold thinking and collaboration. Our commitment to in-person work, typically three days a week, allows us to connect, innovate, and challenge the status quo. We also offer flexibility, balancing office presence with individual needs.

Why Join Us?

At AstraZeneca, we are united by our vision to eliminate cancer as a cause of death. As part of our Oncology R&D team, you will work on pioneering new drug modalities and remain at the cutting edge of biotechnology advancements. We are a science-driven, leading, and decisive Oncology enterprise that pushes the boundaries of medicine to transform the lives of cancer patients. We are committed to creating a collaborative environment where everyone has a voice.

Are you ready to make a meaningful impact in the world of Oncology? Apply today and join us in our mission to eliminate cancer as a cause of death!

Commitment to Diversity and Inclusion:

AstraZeneca embraces diversity and equality of opportunity. We are dedicated to building an inclusive and diverse team that represents a wide range of backgrounds and perspectives. We welcome applications from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment, as well as work authorization and employment eligibility verification requirements.

Join us and be a part of our journey to innovate and lead in the fight against cancer.