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Syneos Health/ inVentiv Health Commercial LLC

Senior Research Associate

Job Description

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3,676 of 10,000 More Like This

Salary Not Available

Position range in Kansas City, MO-KS Metropolitan Statistical Area $132k

  • $194k Per Year Senior Research Associate
    Syneos Health/ inVentiv Health Commercial LLC
Occupation:

Biofuels/Biodiesel Technology and Product Development Managers

Location:

Kansas City, MO

  • 64118
Job Type:

Full Time (30 Hours or More)

Posted:

06/30/2026

Positions available: 1

Source:

FileImport

  • Syneos Health/ inVentiv Health Commercial LLC
Web Site:

commercialcareers.syneoshealth.com

Expires:

10/17/2026

Job #: 25109549MO

Job Requirements and Properties

Help for Job Requirements and Properties. Opens a new window. Work Onsite

Full Time Schedule

Full Time

Job Description

Help for Job Description. Opens a new window. Senior Research Associate

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 Responsibilities

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 SciencesLocation:

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.

Key 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, ...For full information see follow application link.

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