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Senior/Clinical Research Associate

2+ years
Not Disclosed
10 Oct. 22, 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, CPC Certified, 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: Senior/Clinical Research Associate
Location: Sydney or Melbourne
Contract: Full-time, 12-month initial contract

Are you an experienced CRA passionate about making a positive impact through Clinical Research?

Join AstraZeneca and contribute to our Biopharmaceutical pipeline!

About AstraZeneca

Be part of our vision to lead in Cardiovascular, Renal, Metabolism, Respiratory, and Immunology by 2025. We aim to evolve with the healthcare landscape, becoming a digitally-enabled enterprise and accelerating launches. We challenge the status quo, reflect on insights, spot opportunities, and take smart risks.

What You’ll Do

As a Senior/Clinical Research Associate, you will manage sites effectively across various high-profile studies, overseeing all aspects from site selection and start-up to initiation, monitoring, and closure. To succeed in this role, you should possess:

  • Strong knowledge of clinical study management, including monitoring, study drug handling, and data management.
  • Experience working in a similar capacity.
  • Excellent understanding of international guidelines (ICH-GCP), relevant local regulations, and a solid grasp of the drug development process.

Essential Requirements

  • Bachelor’s degree in a related discipline (preferably life sciences) or equivalent qualification.
  • Experience at the CRA level.
  • Familiarity with a risk-based monitoring approach, including remote monitoring.
  • In-depth knowledge of ICH-GCP and basic understanding of GMP/GDP.
  • Sound medical knowledge and ability to learn about relevant AZ Therapeutic Areas.
  • Good understanding of clinical study management, including monitoring, study drug handling, and data management.
  • Strong analytical and problem-solving skills with a solutions-focused mindset.

Desirable Attributes

  • Ability to thrive in a fun, collaborative team environment while also working autonomously.
  • Positive approach to change, seeing it as an opportunity to enhance performance and add value.
  • A champion for continuous improvement, aiming to deliver high-quality clinical trials efficiently.
  • Proven ability to prioritize and manage multiple tasks with conflicting deadlines.

Why AstraZeneca?

At AstraZeneca, we are driven by a shared purpose: pushing the boundaries of science to deliver life-changing medicines to patients worldwide. Our work is meaningful, and we are committed to our people. Our patient-first approach informs all decision-making, and we invest in both team and individual development. We foster an energetic, fast-paced, solutions-focused, and collaborative working environment.

AstraZeneca in Australia is recognized as an Employer of Choice for Gender Equality by the Workplace Gender Equality Agency (WGEA) and as a Bronze Tier Employer within the Australian Workplace Equality Index (AWEI). Visit our ANZ Careers Page to learn more about our commitment to fostering a flexible, diverse, and inclusive environment.

What’s Next?

We want to unlock your potential and inspire you to be your best. Join us to expand your horizons, extend your knowledge, and grow to your fullest.

If you’re curious to learn more, please reach out to Danielle Jones.

Where Can I Find Out More?

Visit our website: AstraZeneca Australia

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive team representing all backgrounds, with a wide range of perspectives. We welcome applications from all qualified candidates and comply with all applicable laws and regulations regarding non-discrimination in employment.