2

Remote Pediatric Clinical Research Jobs (NOW HIRING)

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

... remote work, or add more interesting, diverse pediatric imaging reads to their careers. DESIRED ... clinical value, technology, service, and economics, while elevating the role of radiology and ...

... remote work, or add more interesting, diverse pediatric imaging reads to their careers. DESIRED ... clinical value, technology, service, and economics, while elevating the role of radiology and ...

Pediatric Clinical Dietitian We are looking for team members who are passionate about challenging ... Partial remote work may be available! Provides optimal nutrition care for inpatients and ...

Pediatric Clinical Dietitian We are looking for team members who are passionate about challenging ... Partial remote work may be available! Provides optimal nutrition care for inpatients and ...

New

Pediatric Clinical Dietitian We are looking for team members who are passionate about challenging ... Partial remote work may be available! Provides optimal nutrition care for inpatients and ...

Showing results 21-40

Remote Pediatric Clinical Research information

See salary details

$13

$24

$40

How much do remote pediatric clinical research jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for remote pediatric clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is remote pediatric clinical research?

Remote pediatric clinical research involves conducting studies and trials focused on children's health and medical conditions, but with participants, researchers, or both operating outside of traditional clinical settings. This can include collecting data through telemedicine, digital platforms, or home visits, allowing for greater flexibility and accessibility for families. Remote research aims to improve participation rates, reduce travel burdens, and maintain high standards of data collection and patient safety. It often relies on secure technology to monitor patients, collect consent, and ensure effective communication between healthcare providers and participants.

What are the key skills and qualifications needed to thrive in remote pediatric clinical research?

To excel in Remote Pediatric Clinical Research, you need a strong background in clinical research methodologies, pediatric healthcare, and relevant academic qualifications such as a degree in nursing, medicine, or life sciences. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and certifications like Good Clinical Practice (GCP) are typically required. Strong organizational skills, attention to detail, and effective virtual communication are crucial soft skills for coordinating studies and engaging with pediatric patients and their families remotely. These competencies are essential to ensure regulatory compliance, high-quality data collection, and successful study outcomes in a remote setting.

What are some common challenges faced when working in remote pediatric clinical research, and how can they be managed?

One common challenge in remote pediatric clinical research is maintaining effective communication with both participants' families and multidisciplinary research teams, given the virtual nature of the role. Ensuring data integrity and participant compliance can also be more complex compared to on-site studies. Utilizing secure, user-friendly digital platforms for data collection and regular virtual check-ins helps address these issues. Additionally, remote researchers often collaborate closely with site coordinators and healthcare providers to support families and ensure study protocols are followed, which requires strong organizational and interpersonal skills.

What is the difference between Remote Pediatric Clinical Research vs Remote Pediatric Research Coordinator?

AspectRemote Pediatric Clinical ResearchRemote Pediatric Research Coordinator
CredentialsTypically requires clinical research certifications, healthcare background, or related degreesOften requires research experience, coordination skills, and relevant certifications
Work EnvironmentConducts clinical trials, data analysis, and protocol adherence remotely or in clinical settingsManages participant recruitment, scheduling, and data collection remotely or in clinical sites
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsResearch institutions, hospitals, clinical trial sites

Remote Pediatric Clinical Research involves overseeing and conducting pediatric clinical trials, focusing on data and protocol management. In contrast, Remote Pediatric Research Coordinators handle participant coordination, recruitment, and data collection. Both roles require research experience and certifications but differ in daily responsibilities and focus areas.

More about Remote Pediatric Clinical Research jobs

What cities are hiring for Remote Pediatric Clinical Research jobs?

Cities with the most Remote Pediatric Clinical Research job openings:

What are the most commonly searched types of Pediatric Clinical Research jobs?

The most popular types of Pediatric Clinical Research jobs are:

What states have the most Remote Pediatric Clinical Research jobs?

States with the most job openings for Remote Pediatric Clinical Research jobs include:

Infographic showing various Remote Pediatric Clinical Research job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Senior Clinical Research Associate

WEP Clinical

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Job description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.
 
 
Role Objectives:
The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs. They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential documentation, and keep site and patient data inspection-ready. The Senior CRA builds strong relationships with sponsors and sites, serving as a key point of contact throughout the study. They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist in training or coordinating other CRAs.
 
Complex Study Experience Required 
The Ideal Candidate:
  • Leader
  • Detail Oriented
  • Problem Solver
  • Adaptable
What You'll Do:
  • Contribute to the design and review of study documents (protocols, CRFs, ICFs, and study plans).
  • Lead site feasibility activities: distribute/collect questionnaires, evaluate responses, conduct SQVs, and recommend sites for selection.
  • Planned and conducted SIVs, routine monitoring, and close-out visits in line with protocol, ICH-GCP, and regulatory requirements.
  • Build strong relationships with site staff; deliver training and ongoing guidance on protocol compliance and regulations.
  • Verify source data and CRFs for completeness, accuracy, and consistency; always keep site files audit-ready.
  • Review IP accountability, safety event documentation, and protocol deviations; drive corrective and preventative actions.
  • Manage and resolve data queries, analyze error trends, and provide targeted retraining to prevent recurrence.
  • Track and close action items within study or company timelines; maintain clear oversight of monitoring deliverables.
  • Support investigator meetings and key internal/external meetings; contribute to SOPs, monitoring tools, and templates.
  • (Lead CRA, if assigned) Oversee monitoring on complex studies; develop study-specific monitoring documents (e.g., CMP, deviation plan, report templates); finalize visit reports; train/coordinate CRAs; act as primary clinical monitoring contact for PM/Sponsor and handle CRA escalations.
What You'll Need:
  • Bachelor's degree (life sciences, nursing, or related field preferred)
  • 5-7+ years' experience conducting on-site and remote monitoring visits (or equivalent clinical research experience)
  • Senior CRA levelling: SCRA I (3-5 yrs) - independently manages complex sites; SCRA II (5+ yrs) - oversees complex sites/regions, mentors peers, and drives process improvements
  • Broad therapeutic exposure across multiple study types and indications
  • Strong technical/scientific aptitude with the ability to quickly grasp and execute clinical protocols
  • Advanced organizational and logistical skills; able to manage multiple sites/protocols within budget and timelines
  • Excellent written and verbal communication; confident stakeholder engagement
  • Solid understanding of medical/therapeutic areas and medical terminology
  • Proven ability to train, coach, and mentor clinical research staff
  • Proficient with MS Office and EDC systems; willing to travel up to 80%
  • Ability to remain in a stationary position for extended periods as part of normal day-to-day activities, with reasonable accommodations considered where appropriate 
Location eligibility applies. Candidates must reside in a U.S. state where the company is authorized to hire. This role is not eligible for residents of: California, Colorado, New York, Washington, New Jersey, Massachusetts, Illinois, Hawaii, and District of Columbia. 
 
What We Offer:
Medical, dental, and vision insurance
FSA, HSA
Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
Group short-term and long-term disability insurance
Group Life Insurance
401K safe harbor plan and company match
Paid vacation, holiday, sick and volunteer time
Paid maternity & paternity leave
 
What Sets Us Apart:
WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments. 
 
We're Committed to Our Team:
WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees. 
 
How We Work at WEP Clinical:
At WEP Clinical, we look for individualswho are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment. 
 
Our Services Include:
Access Programs
Clinical Trial Services
Patient Site Solutions
Clinical Trial Supply
Market Access and Commercialization
 
Data Privacy Notice:
WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.
 
Privacy Policy: https://www.wepclinical.com/privacy-policy/
Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/
 
How to Apply:
To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn's Easy Apply option. Please ensure your resume is in English. 
 
Important Note:
To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page (https://www.wepclinical.com/careers/) or our verified LinkedIn page.
 
For Your Safety, Please Note:

We will never communicate with you via Microsoft Teams or text message

We will never ask for your bank account information at any stage of recruitment 

 
WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.
 
WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual's race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
 
#LI-fulltime #LI-remote
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job