Research Sci II RWELP

About the job

Responsible for planning, designing, implementing, and reporting for Real-World Evidence (RWE) and Health Economics & Outcomes Research (HEOR) studies. This includes working closely with pharmaceutical, medical device, and diagnostics clients, among others in the development of project-specific methods and project deliverables. The person in this role will also contribute to face-to-face client meetings, teleconference calls, study design, reporting and publication strategies. RWE clinical study scope includes both prospective and retrospective site-based studies, pragmatic trials, decentralized trials, existing secondary data only studies as well as HEOR projects, including literature reviews, meta-analyses, and medical writing activities

What You'll Do:

- Develop Real-World Evidence study protocols/analysis plans, clinical study reports, abstracts and manuscripts ensuring quality and completeness of client deliverables.

- Lead the conduct of systematic literature reviews and meta-analyses

- Lead studies involving health economics and outcomes research, including patient/provider perspective, patient reported outcomes measures (PROMs), and cost/benefit analyses

- Lead studies utilizing existing secondary data sources (e.g., registries, medical claims, electronic healthcare records). Includes programming requirements, analysis and final reporting writing.

- Interact with clients and team members to determine real-world evidence (RWE) or health economics and outcomes research (HEOR) needs, objectives, and project scope.

- Participate in internal and client launch meetings to understand the project background, study requirements, timelines and deliverables.

- Identify appropriate literature, data sources and tools for research to meet client needs.

- Distill input from clients, clinicians, medical coders, existing data and published literature to assist in the overall study design.

- Provide epidemiologic input into the statistical analysis plan and output required to meet study objectives.

- Responsible for ongoing data review from an epidemiologic standpoint.

- Prepare for and attend expert panels and advisory boards, assist in collection of information and elaboration of meeting reports.

- Responsible for interpreting clinical outcomes research results and providing epidemiologic expertise in using the most appropriate statistical analysis methods for each study.

- Work closely with a statistician in the analysis and reporting of clinical study results

- Prioritize and manage time effectively to meet the needs of multiple clients.

- Work within project budgets and complete high-quality deliverables in a timely manner.

- Assist in developing proposals, including providing input into the scientific rationale, methodology, timelines, and budgets.

- Collaborate with various CTI departments, based on project or study scope

What You'll Bring:

- At least 3 years experience in working in outcomes research and/or epidemiology.

- Masters degree in public health, epidemiology, health services research, pharmacy, nursing, natural science, biostatistics, or closely related discipline

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

Why CTI?

Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.

Please Note

We will never ask for your bank account information at any point during the recruitment process