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Clinical Trial Assistant Remote Jobs in Raleigh, NC

Pricing Analyst (Pricing Analytics)

Durham, NC · On-site +1

$62.80K - $157.10K/yr

... clinical trial sites. * Mentor and train new pricing assistants, pricing analysts, and site contract managers as needed. * Ensure inspection ready by complying with relevant training requirements and ...

Pricing Analyst (Pricing Analytics)

Durham, NC · On-site +1

$62.80K - $157.10K/yr

... clinical trial sites. * Mentor and train new pricing assistants, pricing analysts, and site contract managers as needed. * Ensure inspection ready by complying with relevant training requirements and ...

... Trial Supporting Documents (Protocol Amendments, Investigator Updates, Investigator's Brochure ... Clinical regulatory support H Regulatory operations Q2: Are you open to work remote and open for 4 ...

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Clinical Trial Assistant Remote information

See Raleigh, NC salary details

$11

$36

$66

How much do clinical trial assistant remote jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical trial assistant remote in Raleigh, NC is $36.61, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.73 per hour, depending on experience, location, and employer.

What is a Clinical Trial Assistant Remote job?

A Clinical Trial Assistant (CTA) Remote job involves supporting clinical research teams in coordinating, documenting, and managing clinical trials from a remote location. Responsibilities typically include maintaining regulatory documents, tracking study progress, assisting with patient enrollment, and ensuring compliance with protocols and guidelines. CTAs work closely with Clinical Research Associates (CRAs) and Study Managers to facilitate smooth trial operations. Strong organizational skills, attention to detail, and proficiency with clinical trial management systems (CTMS) are essential for success in this role.

What are the key skills and qualifications needed to thrive in the Clinical Trial Assistant Remote position, and why are they important?

To thrive as a Clinical Trial Assistant Remote, you need a strong foundation in clinical research processes, attention to detail, and familiarity with regulatory compliance, often supported by a degree in life sciences or related field. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of GCP (Good Clinical Practice) guidelines or related certifications is highly beneficial. Excellent organizational skills, proactive communication, and the ability to manage time effectively while working independently are key soft skills. These competencies are crucial for ensuring smooth trial operations, accurate documentation, and effective collaboration with clinical teams from a remote setting.

What does a typical day look like for a Clinical Trial Assistant working remotely?

A typical day for a remote Clinical Trial Assistant involves managing and tracking important study documents, supporting site communications, ensuring data accuracy in trial management systems, and assisting with regulatory submissions. You’ll often coordinate with study coordinators, project managers, and other team members via email and virtual meetings to address queries and maintain trial timelines. The role requires a high level of organization and self-motivation, as you’ll balance multiple administrative tasks and respond quickly to shifting priorities. This collaborative and detail-oriented environment provides opportunities to expand your skills in clinical research and prepare for more advanced roles in the field.
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Infographic showing various Clinical Trial Assistant Remote job openings in Raleigh, NC as of May 2026, with employment types broken down into 84% Full Time, 8% Part Time, and 8% Contract. Highlights an 3% In-person, and 97% Remote job distribution, with an average salary of $76,155 per year, or $36.6 per hour.
Patient Engagement Lead - Global Clinical Trial Recruitment and Retention

Patient Engagement Lead - Global Clinical Trial Recruitment and Retention

Syneos Health/ inVentiv Health Commercial LLC

Morrisville, NC • Remote

$79.80K - $139.60K/yr

Other

Posted 14 days ago


Syneos Health rating

8.5

Company rating: 8.5 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

18th of 70 rated pharmaceutical


Job description

Patient Engagement Lead - Global Clinical Trial Recruitment and Retention

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

Patient Engagement Lead - Global Clinical Trial Recruitment and Retention Location: Remote, U.S.Salary Range: $79,800 - $139,600Overview

The Patient Engagement Lead is a senior-level role responsible for the end-to-end ownership of global patient recruitment and retention (R&R) strategy and execution across clinical trials. This is not a support function-this role is accountable for defining, operationalizing, and delivering recruitment strategy in partnership with sponsors.

You will lead the day-to-day execution of global enrollment strategies, ensuring performance against timelines, budgets, and quality expectations. This role requires a candidate who can step in immediately, operate autonomously, and drive results across complex, global studies.

Key Responsibilities

Full Ownership of Global Recruitment Strategy

  • Own and lead the global patient recruitment and retention strategy across assigned studies from start-up through closeout

  • Translate strategy into execution by driving day-to-day delivery, performance tracking, and continuous optimization

  • Serve as the accountable lead for enrollment outcomes, proactively identifying risks and implementing mitigation plans

Global Program Leadership

  • Lead global, multi-region recruitment programs, ensuring alignment across geographies, study teams, and solution partners

  • Operate as the central point of coordination across stakeholders to ensure seamless execution and delivery

  • Drive consistency and quality in strategy implementation across all regions and phases of the study

Sponsor-Facing Leadership

  • Act as a primary point of contact for sponsors on all recruitment-related activities

  • Provide strategic guidance, performance insights, and clear recommendations to optimize enrollment outcomes

  • Lead discussions on strategy performance, risks, and innovative approaches to accelerate recruitment

Vendor & Partner Oversight

  • Identify and lead selection of recruitment solution partners aligned to study needs and indication

  • Oversee vendor performance, ensuring accountability to scope, timelines, and quality standards

  • Resolve vendor-related challenges independently, maintaining momentum and delivery

Operational Execution & Delivery

  • Own the development and lifecycle management of the Participant Engagement Plan (PEP)

  • Oversee execution of patient-facing tactics, including material development, translation, distribution, and inventory management

  • Ensure all deliverables meet sponsor expectations, regulatory requirements, and internal quality standards

Financial & Project Accountability

  • Manage recruitment-related budgets, forecasts, and scope changes

  • Ensure financial discipline and proactively address out-of-scope activities through appropriate change processes

  • Provide accurate reporting, projections, and updates to support overall study success

Leadership & Continuous Improvement

  • Mentor junior team members and provide oversight where needed

  • Contribute to process improvements, innovation, and departmental growth initiatives

  • Support business development activities, including pre-award strategy and consultation

Required Qualifications
  • Bachelor's degree in Life Sciences, Healthcare, or a related field

  • 5+ years of experience with full ownership of global patient recruitment and retention strategy and execution within clinical research

  • Demonstrated experience serving as the accountable lead for day-to-day delivery of recruitment strategy for sponsors

  • Proven track record managing global, multi-phase clinical trials (Phase I-IV) across a variety of therapeutic areas

  • Experience leading global programs across regions, with accountability for overall management, execution, and results

  • Ability to operate independently and "hit the ground running" in a fast-paced, sponsor-facing environment

  • Strong expertise in data-driven enrollment strategies, including performance tracking and mitigation planning

  • Advanced vendor management experience, including selection, oversight, and performance optimization

  • Demonstrated experience managing budgets, forecasting, and scope changes

  • Excellent communication and stakeholder management skills, with the ability to influence at all levels

Preferred Qualifications
  • Experience supporting pre-award strategy and feasibility

  • Background in patient advocacy and community engagement initiatives

  • Experience contributing to innovation in patient recruitment approaches

Why Join Us

You'll join a highly collaborative, supportive, and growth-oriented team that values ownership, innovation, and continuous development. This is an opportunity to take full accountability for global recruitment strategy while working alongside experienced leaders committed to your success and career progression!

Get to know Syneos Health


Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.


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