Senior Project Specialist - Real World Evidence (S

at Syneos Health LLC in Chicago, Illinois, United States

Job Description

Senior Project Specialist - Real World Evidence (Sponsor Dedicated /Remote -US Based)

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
Senior Project Specialist - Real World Evidence (Sponsor Dedicated /Remote -US Based)

Are you looking to grow your career in one of the fastest-evolving areas of clinical research and healthcare analytics?

We are seeking a Senior Project Specialist - Real World Evidence (RWE) to join a sponsor-dedicated team supporting innovative pharmaceutical research programs focused on real-world data and evidence generation. This role is ideal for someone who enjoys organization, coordination, problem-solving, and working behind the scenes to help complex research programs run smoothly.

While this is an administrative and operational support-focused position, it is important that candidates already have exposure to the Real World Evidence (RWE) space and understand the fundamentals of how RWE studies and teams operate.

This could be a great fit for someone who has supported:

Real World Evidence (RWE) teams

Epidemiology or observational research programs

Outcomes research initiatives

Data Management teams within Pharmaceutical, Biotechnology, or CRO environments
and is looking to continue building their career in this exciting and growing specialty area.
What You'll Be Doing

In this role, you will support project teams responsible for both:

Secondary data studies

Primary data collection studies

You'll work closely with Project Leads, epidemiologists, data analysts, Data Management teams, and cross-functional stakeholders to help keep projects organized, on track, and moving forward.

Your day-to-day work may include:

Coordinating and updating study milestones and timelines

Supporting project tracking within CTMS systems

Scheduling and coordinating meetings

Preparing meeting minutes and follow-up action items

Helping teams stay organized across multiple deliverables

Supporting operational activities for ongoing RWE studies

Assisting with documentation, reporting, and project coordination

Helping facilitate communication between study teams, analysts, and stakeholders

This is a highly collaborative role where organization, communication, and attention to detail are key.
What We're Looking For

Required

Prior experience supporting work within:

Real World Evidence (RWE)

Clinical Data Management

Epidemiology

Observational or outcomes research environments

Experience within a Pharmaceutical, Biotechnology, or CRO setting

Understanding of:

Secondary data research

Primary data collection studies

CTMS systems and/or clinical research operations

Strong organizational and coordination skills

Ability to manage multiple tasks and deadlines in a fast-paced environment

Strong communication and interpersonal skills

Proficiency with Microsoft Office applications

Experience with Late Phase and RWE projects supporting regulatory purposes, including pivotal or supportive evidence generation, is considered a strong asset

Nice to Have (But Not Required)

Experience working directly with epidemiology or data analytics teams

Sponsor-dedicated or embedded team... For full info follow application link.