Senior Research Associate

Syneos Health•Unorganized Thunder Bay District, ON

18h•Hybrid

About The Position

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. JOB TITLE: Research Associate/Senior Research Associate, Real World Evidence SELECT ONE: Clinical Solutions JOB CODE: SH1317/ SH1323 REPORTS TO: Associate Director, Real World Evidence; or designee Business Unit: Real World & Late Phase (RWLP) Industry: Life Sciences Location: US or Canada (Hybrid/Remote) Position Overview The Research Associate/Senior Research Associate, Real World Evidence (RWE) is part of the global Real World & Late Phase (RWLP) Business Unit, supporting the generation of real-world evidence, and patient outcomes evidence across the drug development lifecycle. In this role, you will contribute to and or lead real-world research initiatives that inform clinical strategy, regulatory engagement, and market access decisions for life sciences clients. Working closely with senior team members, you will support the design and execution of retrospective and prospective studies while developing your expertise in RWE and outcomes research methodologies. This position is well suited to professionals seeking meaningful exposure to or to deepen their expertise in evidence generation within a collaborative, well-supported team environment that values high-quality work and sustainable performance.

Requirements

Master’s degree in public health, epidemiology, health sciences, or a related field (or equivalent combination of education and experience).
1–2 years (Research Associate), or 2+ years (Senior Research Associate) of relevant experience within the life sciences industry (e.g., HEOR, RWE, clinical research, pharmaceutical industry, healthcare consulting, or academia).
Foundational understanding of real-world research methodologies and study design.
Overall understanding of the drug development lifecycle.
Strong analytical and critical thinking skills.
Proficiency in Microsoft Excel, Word, and PowerPoint.
Working knowledge of statistical software (e.g., SAS, R, Stata, or similar).
Business-level conversational English (written and spoken).

Nice To Haves

Graduate degree (Master’s or PhD) in a relevant discipline.
Academic or industry research experience.
Conducting analyses in databases and/or registries

Responsibilities

Contribute to study design and methodology development
Develop innovative approaches, frameworks and solutions to client problems
Deliver project outputs that meet established quality standards, timelines, and budget requirements.
Conduct structured literature reviews and targeted secondary research to support RWE initiatives.
Participate in qualitative research activities, including patient interviews, to generate actionable healthcare insights.
Analyze and interpret qualitative and quantitative ‘real-world’ data for deliverables
Conduct workshops and moderate discussions
Present results to external clients
Contribute to the development of: Study protocols, Technical reports, Manuscripts and scientific posters, Client presentations
Develop and format materials using PowerPoint, Word, and Excel.
Summarize and synthesize complex clinical and outcomes data into clear, structured findings.
Support retrospective and prospective real-world studies under senior guidance.
Demonstrate openness to leveraging emerging technologies, including AI-enabled tools, to improve efficiency, analytical rigor, and personal productivity.