At a Glance
- Tasks: Design and conduct epidemiological studies to generate real-world evidence in oncology.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Remote work, access to global network, and opportunities for professional growth.
- Other info: Collaborate with a dedicated sponsor and gain deep expertise in their therapies.
- Why this job: Make a real impact on patient outcomes while advancing your career in healthcare.
- Qualifications: PhD in Epidemiology or related field with relevant experience in cancer studies.
The predicted salary is between 60000 - 80000 £ per year.
Location: Remote, candidates must be based in one of the selected locations. Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
Core Function Description:
- Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies.
- Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.
- Lead, design, and manage epidemiological, biomarker and/or data science projects.
- Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries).
- Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
- Construct cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed.
- Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers.
- Support the effective communication of study/analysis results to support internal and external decisions.
- Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
- Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.
Technical Expertise:
- Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes.
- Ability to design studies independently, (i.e., ability to translate research questions to create study design).
Subject Matter Expertise:
- Extensive experience conducting cancer epidemiology studies (solid tumor experience a plus), experience with commercial Oncology EMR databases.
- Leverage RWE expertise to identify evidence gaps and develop options to address the evidence gaps in support of Clinical Development Programs in early phase (ph1/2).
- Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, registry data) for methodologic research questions.
- Expert knowledge and extensive experience with cancer epi (solid tumor experience a plus), extensive experience with oncology EMR databases, extensive experience with conducting cancer epi studies.
- Experience with Clinico-genomic multi-modal data (e.g., Tempus AI) or population biobank data (UK biobank) is a plus.
Minimum Qualifications:
- PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment.
- Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.
- Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.
- Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.
- A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.
- Demonstrated ability to function with an increasing level of autonomy and to develop productive cross-functional collaborations in a matrix environment.
- Ability to manage priorities and performance targets.
- Experience in leading drug development project for 2+ years for therapeutic area of assignment preferred.
What’s in it for you?
- Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
- Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
- Access IQVIA’s global network who supports your growth.
- This is your chance to make an impact, while building a career that matters.
Senior Epidemiologist, Oncology (FSP Sponsor Dedicated) in London employer: IQVIA
At IQVIA, we pride ourselves on being a forward-thinking employer that empowers our employees to make a meaningful impact in healthcare. As a Senior Epidemiologist in our Sponsor-Dedicated FSP team, you will enjoy a collaborative work culture that fosters professional growth and offers access to a global network of expertise. With opportunities to lead innovative research projects and contribute to evidence-based healthcare, you'll be part of a mission-driven organisation dedicated to improving patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Epidemiologist, Oncology (FSP Sponsor Dedicated) in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at IQVIA or similar companies. A friendly chat can lead to insider info about the role and even a referral!
✨Tip Number 2
Prepare for the interview by diving deep into the company's projects and values. Show us that you understand how your expertise in epidemiology can directly contribute to improving patient outcomes.
✨Tip Number 3
Practice your storytelling skills! Be ready to share specific examples of your past work, especially those related to cancer epidemiology. We want to hear how you've tackled challenges and made an impact.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows us you’re serious about joining our team and making a difference in healthcare.
We think you need these skills to ace Senior Epidemiologist, Oncology (FSP Sponsor Dedicated) in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Epidemiologist role. Highlight your experience in epidemiological studies, especially in oncology, and showcase any relevant projects you've led. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about real-world evidence and how your background makes you a perfect fit for this role. Let us know what excites you about working with one sponsor and advancing healthcare.
Showcase Your Research Skills:Since this role involves designing and conducting studies, be sure to highlight your research skills. Mention specific methodologies you've used and any significant findings from your past work. We love seeing concrete examples of your expertise!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about our team and values!
How to prepare for a job interview at IQVIA
✨Know Your Epidemiology Inside Out
Make sure you brush up on your epidemiological methods and real-world evidence (RWE) knowledge. Be prepared to discuss how you've designed studies in the past, especially in oncology. Highlight any specific experiences with solid tumours or EMR databases, as these will be key to impressing the interviewers.
✨Showcase Your Project Leadership Skills
Since this role involves leading projects, come ready with examples of how you've successfully managed epidemiological studies or data science projects. Talk about your experience in developing study protocols and analysis plans, and how you’ve navigated challenges during project execution.
✨Communicate Clearly and Effectively
You’ll need to convey complex research findings to various stakeholders. Practice explaining your past research results in a straightforward manner. Think about how you can simplify technical jargon without losing the essence of your work, as this will demonstrate your ability to communicate effectively.
✨Prepare Questions That Show Your Interest
Interviews are a two-way street! Prepare thoughtful questions that show your genuine interest in the company and the role. Ask about their current RWE strategies or how they envision the future of oncology research. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.
