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Remote Ppd Clinical Research Jobs (NOW HIRING)

The IMA Group

Clinical Research Patient Recruiter - Remote

$23 - $25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Description Clinical Research Patient Recruiter Remote $23-$25/hour Full-Time Are you confident on the phone and motivated by connecting with people? IMA Clinical Research is seeking an energetic ...

The IMA Group

Clinical Research Patient Recruiter - Remote

$23 - $25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Clinical Research Patient Recruiter Remote | $23-$25/hour | Full-Time Are you confident on the phone and motivated by connecting with people? IMA Clinical Research is seeking an energetic, personable ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

  • Medical

  • Life

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 ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring ...

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How much do remote ppd clinical research jobs pay per year?

As of Aug 17, 2026, the average yearly pay for remote ppd clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a remote PPD Clinical Research professional?

A Remote PPD Clinical Research job involves working for PPD (Pharmaceutical Product Development), a global contract research organization, to support clinical trials and research projects from a remote location. Professionals in this role help design, manage, and monitor clinical studies to ensure compliance with protocols, regulatory standards, and data integrity. Responsibilities may include data management, coordinating with study sites, and supporting trial documentation. Working remotely allows employees to collaborate with international teams and clients while maintaining flexibility. This role is essential in advancing new treatments and therapies to market efficiently and safely.

How does working remotely as a PPD Clinical Research professional impact collaboration with on-site teams and study sites?

As a remote PPD Clinical Research professional, you will collaborate closely with on-site teams, investigators, and study coordinators through virtual communication platforms. While you may not be physically present, regular video calls, emails, and project management tools are used to maintain effective communication and ensure study protocols are followed. Adapting to different time zones and proactively addressing challenges in real-time are common aspects of the role. Strong organizational and interpersonal skills are essential for building trust and maintaining seamless coordination across dispersed teams.

What are the key skills and qualifications needed to thrive as a remote PPD Clinical Research professional?

To excel as a Remote PPD Clinical Research professional, you need a comprehensive understanding of clinical trial processes, regulatory guidelines (such as GCP), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and certifications like ACRP or SOCRA are typically valuable. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing studies and collaborating with distributed teams. These competencies ensure compliance, data integrity, and the successful execution of clinical research in a remote environment.
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Remote Ppd Clinical Research jobs near you
Infographic showing various Remote Ppd Clinical Research job openings in the United States as of August 2026, with employment types broken down into 2% Internship, 76% Full Time, 10% Part Time, and 12% Contract. Highlights an 2% In-person, and 98% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Senior Clinical Research Associate - CNS

Cognitive Research Corporation

Remote

Full-time

Re-posted 10 days ago

Job description

The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Essential Duties & Responsibilities
  • Initiates, monitors, and closes-out investigative sites in accordance with FDA/ICH regulations.
  • Tracks and maintains study specific non-Case Report Form database
  • Administers Clinical research projects; collects investigator documentation, site management, clinical contact, and prepare reports as required
  • Ensures appropriate source document review and source document verification as required
  • Reviews Case Report Forms to identify erroneous, missing, or incomplete data
  • Generates queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly
  • Verifies study drug accountability; generates and tracks drug shipments and storage
  • Travels as necessary, based on project needs and according to Clinical Monitoring Plan requirements
  • Performs data collection, retrieval, entry and clean up as necessary
  • Develops and maintains strong relationships with Investigator(s) and site staff
  • Independently manages sites resulting in acceptable Quality Assurance reports.
  • Escalates study/site issues/deviations appropriately
  • Serves as lead monitor for a protocol or project by creating study files, arranges monitoring schedules, leads the project team, organize and run meetings and performs other project management duties as assigned by management
  • Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format
  • Reports, writes narratives, and follows-up on reported serious adverse events
  • Interacts and attends client meetings, as appropriate
  • Mentors junior staff/CRAs
  • Quality oversight checks of monitoring
  • Performs other duties as assigned

Qualifications
  • Bachelor's degree, or RN, in a related field or equivalent combination of education, training and experience
  • Minimum 5 years' experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
  • Ability to work and travel independently with minimal supervision
  • Experience with numerous EDC systems.
  • Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Office, Zoom and Adobe
  • Excellent writing and verbal skills, English language proficiency
  • Meticulous attention to detail
  • Time management and ability to prioritize tasks
  • Ability to travel up to 70%

Department Clinical Operations Role Senior Clinical Research Associate Locations Remote, US Remote status Fully Remote Employment type Full-time

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